Abstract
Soybean (Glycine max (L.) Merrill) is the most widely cultivated oilseed crop accounting for more than 50 % of the world’s oilseed production. Yield gain in soybean estimated to be 0.5–0.7 % per year in North America has been driven by the adoption of agronomic or management practices and genetic improvement. While genetic improvement through breeding will continue to play a significant role in enhancing yield by the development of cultivars adapted to a wide range of latitudes, biotech traits such as enhanced insect protection and weed control contribute indirectly to yield improvement. An understanding of physiological traits associated with genetic gain in yield offers vast opportunities for further advances in yield improvement. Potential targets for genetic improvement include source capacity (leaf area index, leaf area duration, carbon and nitrogen assimilation, and dry matter partitioning), sink strength (number of primary and secondary yield components, seed-filling rate and duration), and tolerance to suboptimal conditions (water limitation and high/low temperature). Manipulating single or multiple traits using breeding and biotechnology approaches will help to improve intrinsic yield potential and yield stability traits in soybean. Application of multiple technologies to improve yield gain is vital, with the changing climatic conditions and increasing global demand for food and feed.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Abogadallah G, Nada R, Malinowski R, Quick P (2011) Overexpression of HARDY, an AP2/ERF gene from Arabidopsis, improves drought and salt tolerance by reducing transpiration and sodium uptake in transgenic Trifolium alexandrinum L. Planta 233:1265–1276
Ackerson RC, Havelka UD, Boyle MG (1984) CO2-enrichment effects on soybean physiology II Effects of stage-specific CO2 exposure. Crop Sci 24:1150–1154
Ainsworth EA, Yendrek CR, Skoneczka JA, Long SP (2012) Accelerating yield potential in soybean: potential targets for biotechnological improvement. Plant Cell Env 35:38–52
Alvim FC, Carolino SMB, Cascardo JCM, Nunes CC, Martinez CA, Otoni WC, Fontes EPB (2001) Enhanced accumulation of BiP in transgenic plants confers tolerance to water stress. Plant Physiol 126:1042–1054
Andrade FH, Ferreiro M (1996) Reproductive growth of maize, sunflower and soybean at different source levels during grain filling. Field Crops Res 48:155–165
Aref S, Pike DR (1998) Midwest farmers’ perceptions of crop pest infestations. Agron J 90:819–825
ASA (2013) Introduction American Soybean Association, St Louis, Missouri. http://soystats.com. Accessed May 2014
Asada K (2006) Production and scavenging of reactive oxygen species in chloroplasts and their functions. Plant Physiol 141:391–396
Atkins CA, Smith PM (2007) Translocation in legumes: assimilates, nutrients, and signaling molecules. Plant Physiol 144:550–561
Badawi GH, Kawano N, Yamauchi Y, Shimada E, Sasaki R, Kubo A, Tanaka K (2004) Over-expression of ascorbate peroxidase in tobacco chloroplasts enhances the tolerance to salt stress and water deficit. Physiol Plant 121:231–238
Bahieldin A, Mahfouz HT, Eissa HF, Saleh OM, Ramadan AM, Ahmed IA et al (2005) Field evaluation of transgenic wheat plants stably expressing the HVA1 gene for drought tolerance. Physiol Plant 123:421–427
Bakhetia M, Urwin PE, Atkinson HJ (2007) qPCR analysis and RNAi define pharyngeal gland cell-expressed genes of Heterodera glycines required for initial interactions with the host. Mol Plant Microbe Int 20:306–312
Bao AK, Wang SM, Wu GQ, Xi JJ, Zhang JL, Wang CM (2009) Overexpression of the Arabidopsis H+ PPase enhanced resistance to salt and drought stress in transgenic alfalfa (Medicago sativa L). Plant Sci 176:232–240
Bartels D, Sunkar R (2005) Drought and salt tolerance in plants. Crit Rev Plant Sci 24:23–58
Baud S, Wuilleme S, Lemoine R, Kronenberger J, Caboche M, Lepiniec L, Rochat C (2005) The AtSUC5 sucrose transporter specifically expressed in the endosperm is involved in early seed development in Arabidopsis. Plant J 43:824–836
Board JE, Harville BG (1998) Late-planted soybean yield response to reproductive source/sink stress. Crop Sci 38:763–771
Board JE, Kahlon CS (2011) Soybean yield formation: what controls it and how it can be improved. In: El-Shemy HA (ed.) Soybean physiology and biochemistry. Intech publishing, pp. 1–36. http://www.intechopen.com/articles/show/title/soybean-yield-formation-what-controls-itand-how-it-can-be-improved
Board JE, Wier AT, Boethel DJ (1994) Soybean yield reductions caused by defoliation during mid to late seed filling. Agron J 86:1074–1079
Board JE, Wier AT, Boethel DJ (1995) Source strength influence on soybean yield formation during early and late reproductive development. Crop Sci 35:1104–1110
Board JE, Kumudini S, Omielan J, Prior E, Kahlon CS (2010) Yield response of soybean to partial and total defoliation during the seed-filling period. Crop Sci 50:703–712
Boerma RL (1979) Comparison of past and recently developed soybean cultivars in maturity groups VI, VII and VIII. Crop Sci 19:611–613
Bortiri E, Chuck G, Vollbrecht E, Rocheford T, Martienssen R, Hake S (2006) ramosa2 encodes a LATERAL ORGAN BOUNDARY domain protein that determines the fate of stem cells in branch meristems of Maize. Plant Cell 18:574–585
Boyer JS (1982) Plant productivity and environment. Science 218:443–448
Capell T, Bassie L, Christou P (2004) Modulation of the polyamine biosynthetic pathway in transgenic rice confers tolerance to drought stress. Proc Natl Acad Sci U S A 101:9909–9914
Carlson DR, Brun WA (1984) Alteration of C-assimilate partitioning in leaves of soybeans having increased reproductive loads at one node. Plant Physiol 75:887–890
Castiglioni P, Warner D, Bensen RJ, Anstrom DC, Harrison J, Stoecker M, Abad M, Kumar G, Salvador S, D’Ordine R et al (2008) Bacterial RNA chaperones confer abiotic stress tolerance in plants and improved grain yield in maize under water-limited conditions. Plant Physiol 147:446–455
Caviness CE, Thomas JD (1980) Yield reduction from defoliation of irrigated and non-irrigated soybeans. Agron J 72:977–980
Century K, Reuber TL, Ratcliffe OJ (2008) Regulating the regulators: the future prospects for transcription factor based agricultural biotechnology products. Plant Physiol 147:20–29
Chen LM, Li KZ, Miwa T, Izui K (2004) Overexpression of a cyanobacterial phosphoenol pyruvate carboxylase with diminished sensitivity to feedback inhibition in Arabidopsis changes in amino acid metabolism. Planta 219:440–449
Chen Z, Hong X, Zhang H, Wang Y, Li X, Zhu JK, Gong Z (2005) Disruption of the cellulose synthase gene, AtCesA8/IRX1, enhances drought and osmotic stress tolerance in Arabidopsis. Plant J 43:273–283
Chen H, Hwang JE, Lim CJ, Kim DY, Lee SY, Lim CO (2010) Arabidopsis DREB2 C functions as a transcriptional activator of HsfA3 during the heat stress response. Biochem Biophys Res Commun 401:238–244
Chincinska IA, Liesche J, Krugel U, Michalska J, Geigenberger P, Grimm B, Kuhn C (2008) Sucrose transporter StSUT4 from potato affects flowering, tuberization and shade avoidance response. Plant Physiol 146:515–528
Chinnusamy V, Schumaker K, Zhu JK (2004) Molecular genetic perspectives on cross-talk and specificity in abiotic stress signaling in plants. J Exp Bot 55:225–236
Cho MH, Jang A, Bhoo SH, Jeon JS, Hahn TR (2012) Manipulation of triose phosphate/phosphate translocator and cytosolic fructose-1,6-bisphosphatase, the key components in photosynthetic sucrose synthesis, enhances the source capacity of transgenic Arabidopsis plants. Photosynthesis Res 111:261–268
Choi JY, Seo YS, Kim SJ, Kim WT, Shin JS (2011) Constitutive expression of CaXTH3, a hot pepper xyloglucan endotransglucosylase/ hydrolase, enhanced tolerance to salt and drought stresses without phenotypic defects in tomato plants (Solanum lycopersicum cv Dotaerang). Plant Cell Rep 30:867–877
Clement M, Lambert A, Herouart D, Boncompagni E (2008) Identification of new up-regulated genes under drought stress in soybean nodules. Gene 426:15–22
Collier R, Tegeder M (2012) Soybean ureide transporters play a critical role in nodule development, function and nitrogen export. Plant J 72:355–367
Coombe BG (1976) The development of fleshy fruits. Ann Rev Plant Physiol 27:507–528
Cortina C, Culianez-Macia F (2005) Tomato abiotic stress enhanced tolerance by trehalose biosynthesis. Plant Sci 169:75–82
Dalley CD, Kells JJ, Renner KA (2001) Weed interference in glyphosate resistant soybean and corn as influenced by timing of weed control and crop row spacing. Weed Sci Soc Am 41:5
De Bruin JL, Pedersen P (2009) Growth, yield and yield component changes among old and new soybean cultivars. Agron J 101:124–130
de Souza PI, Egli DB, Bruening WP (1997) Water stress during seed filling and leaf senescence in soybean. Agron J 89:807–812
Desclaux D, Huynh TT, Roumet P (2000) Identification of soybean plant characteristics that indicate the timing of drought stress. Crop Sci 40:716–722
Desimone M, Catoni E, Ludewig U, Hilpert M, Schneider A, Kunze R, Tegeder M, Frommer WB, Schumacher K (2002) A novel superfamily of transporters for allantoin and other oxo derivatives of nitrogen heterocyclic compounds in Arabidopsis. Plant Cell 14:847–856
Ding X, Gopalakrishnan B, Johnson LB, White FF, Wang X, Morgan TD, Kramer KJ, Muthukrishnan S (1998) Insect resistance of transgenic tobacco expressing an insect chitinase gene. Trans Res 7:77–84
Doebley J, Gaut BS, Smith BD (2006) The molecular genetics of crop domestication. Cell 127:1309–1321
Dogan E, Kirnak H, Copur O (2007) Deficit irrigations during soybean reproductive stages and CROPGRO-soybean simulations under semi-arid climatic conditions. Field Crop Res 103:154–159
Dornbos DL, Mullen RE, Shibles RM (1989) Drought stress effects during seed fill on soybean seed germination and vigor. Crop Sci 29:476–480
Doyle MR, Davis SJ, Bastow RM, McWatters HG, Kozma-Bognar L, Nagy F, Millar AJ, Amasino RM (2002) The ELF4 gene controls circadian rhythms and flowering time in Arabidopsis thaliana. Nature 419:74–77
Du H, Wang N, Cui F, Li X, Xiao J, Xiong L (2010) Characterization of the β-carotene hydroxylase gene DSM2 conferring drought and oxidative stress resistance by increasing xanthophylls and abscisic acid synthesis in rice. Plant Physiol 154:1304–1318
Edwards GE, Furbank RT, Hatch MD, Osmond CB (2001) What does it take to be C4? Lessons from the evolution of C4 photosynthesis. Plant Physiol 125:46–49
Egli DB (1998) Seed biology and the yield of grain crops. CAB, Wallingford, p 178
Egli DB (1999) Variation in leaf starch and sink limitations during seed filling in soybean. Crop Sci 39:1361–1368
Egli DB, Bruening WP (2001) Source-sink relationships, seed sucrose levels and seed growth rates in soybean. Ann Bot 88:235–242
Egli DB, Donald LS (2004) Seed-fill duration and yield of grain crops. Advances in agronomy. Academic, Waltham, pp 243–279
Egli DB, Leggett JE (1976) Rate of dry matter accumulation in soybean seed with varying source-sink ratios. Agron J 68:371–374
Egli DB, Leggett JE (1985) Nitrogen mobilization during seed fill in soybeans. In: Shibles R (ed) Proceedings of the third world soybean research conference, Ames. Westview, Boulder, pp 884–890
Egli DB, Leggett JE, Cheniae A (1980) Carbohydrate levels in soybean leaves during reproductive growth. Crop Sci 20:468–473
Egli DB, Ramseur EL, Zhenwen Y, Sullivan CH (1989) Source-sink alterations affect the number of cells in soybean cotyledons. Crop Sci 29:732–735
Evans LT (1975) Beyond photosynthesis-the role of respiration, translocation and growth potential in determining productivity. In: Cooper IP (ed) Photosynthesis and productivity in different environments. Cambridge University Press, Cambride, pp 501–507
Evans LT (1993) Crop evolution, adaptation, and yield. Cambridge University Press, Cambridge, pp 500
Evans LT, Fischer RA (1999) Yield potential: its definition, measurement and significance. Crop Sci 39:1544–1551
FAO (2013) Crop water information:Soybean. In FAO water, land and water division.http://www.fao.org/nr/water/cropinfo_soybean.html
Farrar JF (1988) Temperature and the partitioning and translocation of carbon. In: Long SP, Woodward FI (eds) Plants and temperature. Symposium of the society of experimental biology 42. Company of Biologists, Cambridge, pp 203–235
Fehr WR, Caviness CE (1981) Reproductive stages of soybean development. Iowa State University Cooperative Extension, Ames, pp 6–7
Feng L, Han Y, Liu G, An B, Yang J, Yang G et al (2007) Overexpression of sedoheptulose-1,7-bisphosphatase enhances photosynthesis and growth under salt stress in transgenic rice plants. Func Plant Biol 34:822–834
Fischer RA, Edmeades GO (2010) Breeding and cereal yield progress. Crop Sci 50:85–98
Floyd RA, Nagy ZS (1984) Formation of long lived hydroxyl free radical adducts of proline and hydroxy-proline in a Fenton reaction. Biochem Biophys Acta 790:94–97
Foulkes MJ, Reynolds MP, Sylvester-Bradley R (2009) Genetic improvement of grain crops: yield potential. In: Sadras VO, Calderini DF (eds) Crop physiology: applications for genetic improvement and agronomy. Elsevier, Burlington, pp 355–385
Froissard M, Belgareh-Touze N, Buisson N, Desimone M, Frommer WB, Haguenauer-Tsapis R (2006) Heterologous expression of a plant uracil transporter in yeast: improvement of plasma membrane targeting in mutants of the Rsp5p ubiquitin protein ligase. Biotechnol J 1:308–320
Fu JM, Zhang GL, Su F, Wang ZL, Dong Y, Shi CY (1999) Partitioning of 14 C-Assimilates and effects of source-sink manipulation at seed-filling in soybean. Acta Agronomica Sinica 25:170–173 (Chinese)
Gao SQ, Chen M, Xia LQ, Xiu HJ, Xu ZS, Li LC, Zhao CP, Cheng XG, Ma YZ (2009) A cotton (Gossypium hirsutum) DRE-binding transcription factor gene, GhDREB, confers enhanced tolerance to drought, high salt, and freezing stresses in transgenic wheat. Plant Cell Rep 28:301–311
Gao SQ, Chen M, Xu ZS, Zhao CP, Li LC, Xu HJ, Tang YM, Zhao X, Ma YZ (2011a) The soybean GmbZIP1 transcription factor enhances multiple abiotic stress tolerances in transgenic plants. Plant Mol Biol 75:537–553
Gao T, Wu Y, Zhang Y, Liu L, Ning Y, Wang D, Tong H, Chen S, Chu C, Xie Q (2011b) OsSDIR1 overexpression greatly improves drought tolerance in transgenic rice. Plant Mol Biol 76:145–156
Garay AF, Wilhelm WW (1983) Root system characteristics of two soybean isolines undergoing water stress conditions. Agron J 75:973–977
Garg AK, Kim JK, Owens TG, Ranwala AP, Choi YD, Kochian LV, Wu RJ (2002) Trehalose accumulation in rice plants confers high tolerance levels to different abiotic stresses. Proc Natl Acad Sci U S A 99:15898–15903
Gatehouse LN (1995) Novel genes for insect resistance in transgenic plants. PhD Thesis University of Durham, UK
Gatehouse AMR, Shi Y, Powell KS, Brough C, Hilder VA, Hamilton WDO et al (1993) Approaches to insect resistance using transgenic plants. Phil Trans Roy Soc Lond 342:279–286
Gbikpi PJ, Crookston RK (1981) Effect of flowering date on accumulation of dry matter and protein in soybean seeds. Crop Sci 21:652–655
Gifford RM, Evans LT (1981) Photosynthesis, carbon partitioning and yield. Ann Rev Plant Physiol 32:485–509
Giroux MJ, Shaw J, Barry G, Cobb GB, Greene T, Okita T, Hannah CL (1996) A single gene mutation that increases maize seed weight. Proc Natl Acad Sci U S A 93:5824–5829
Goli A, Weaver DB (1986) Defoliation responses of determinate and indeterminate late planted soybean. Crop Sci 26:156–159
Good AG, Johnson SJ, DePauw M, Carroll RT, Savidov N, Vidmar JJ, Lu Z, Taylor GT, Stroeher V (2007) Engineering nitrogen use efficiency with alanine aminotransferase. Can J Bot 85:252–262
Gordon AJ, Ryle GJA, Mitchell DF, Powell CE (1985) The flux of 14C labeled photosynthate through soybean root nodules during N2 fixation. J Exp Bot 36:756–769
Greb T, Clarenz O, Schafer E, Muller D, Herrero R, Schmitz G, Theres K (2003) Molecular analysis of the lateral suppressor gene in Arabidopsis reveals a conserved control mechanism for axillary meristem formation. Genes Dev 17:1175–1187
Grossi-de-Sa MF, Pelegrini PB, Fragoso RR (2011) Genetically modified soybean for insect-pests and disease control. In: Sudaric A (ed) Soybean—molecular aspects of breeding. ISBN:978-953-307-240-1, InTech, Rijeka
Gubis R, Vankova V, Cervena M, Dragunova M, Hudcovicova H, Lichtnerovia et al (2007) Transformed tobacco plants with increased tolerance to drought. South Afr J Bot 73:505–511
Guo Q, Zhang J, Gao Q, Xing S, Li F, Wang W (2008) Drought tolerance through overexpression of monoubiquitin in transgenic tobacco. J Plant Physiol 165:1745–1755
Haigler CH, Singh B, Zhang D, Hwang S, Wu C, Cai WX et al (2007) Transgenic cotton over-producing spinach sucrose phosphate synthase showed enhanced leaf sucrose synthesis and improved fiber quality under controlled environmental conditions. Plant Mol Biol 63:815–832
Halpin C (2005) Gene stacking in transgenic plants—the challenge for 21st century plant biotechnology. Plant Biotech J 3:141–155
Han T, Wu C, Tong Z, Mentreddy RS, Tan K, Gai J (2006) Post flowering photoperiod regulates vegetative growth and reproductive development of soybean. Env Exp Bot 55:120–129
Hanway JJ, Thompson HE (1967) How a soybean plant develops. Iowa State University Special Report, Ames, pp 20
Harding JA (1976) Heliothis species: seasonal occurrence, hosts and host importance in the lower Rio Grande Valley. Env Ent 5:666–668
Hardman LL, Brun WA (1971) Effect of atmospheric carbon dioxide enrichment at different developmental stages on growth and yield components of soybean. Crop Sci 11:886–888
Harper JE (1987) Nitrogen metabolism. In: Wilcox JR (ed) Soybeans: improvement, production, and uses. 2nd edn. ASA, Madison, pp 497–533
Hartman GL, Hill CB (2010) Diseases of soybean and their management. In: Singh G (ed) Soybean: botany, production, and uses. CAB, Wallingford, pp 276–299
Hartman GL, Wang TC, Tschanz AT (1991) Soybean rust development and the quantitative relationship between rust severity and soybean yield. Plant Dis 75:596–600
Hartman GL, Sinclair JB, Rupe JC (1999) (eds) Compendium of soybean diseases, 4th edn. American Phytopathological Society, St Paul, pp 1–128
Hartman GL, West ED, Herman TK (2011) Crops that feed the World 2 Soybean—worldwide production, use and constraints caused by pathogens and pests. Food Sec 3:5–17
He CM, Zhang WW, Gao QA, Yang AF, Hu XR, Zhang JR (2011) Enhancement of drought resistance and biomass by increasing the amount of glycine betaine in wheat seedlings. Euphytica 177:151–167
Heatherly LG, Elmore RW (2004) Managing inputs for peak production. In: Boerma HR, Specht JE (eds) Soybean: improvement, production and uses. ASA, Madison, pp 451–536
Heindl JC, Brun WA (1983) Light and shade effects on abscission and C-photoassimilate partitioning among reproductive structures in Soybean. Plant Physiol 73:434–439
Henderson JB, Kamprath EJ (1970) Nutrient and dry matter accumulation by soybean. Technical Bulletin. North Carolina State University Agricultural Experiment Station, Raleigh, pp 27
Heyer AG, Raap M, Schoreer B, Marty B, Willmitzer L (2004) Cell wall invertase expression at the apical meristem alters floral, architectural, and reproductive traits in Arabidopsis thaliana. Plant J 39:161–169
Hibberd JM, Sheehy JE, Langdale JA (2008) Using C4 photosynthesis to increase the yield of rice—rationale and feasibility. Curr Opin Plant Biol 11:228–231
Hicks DR, Pendleton JW (1969) Effect of floral bud removal on performance of soybeans. Crop Sci 9:435–437
Higley LG, Boethel DJ (1994) Handbook of soybean insect pests. The Entomological Society of America, Maryland, pp 1–10
Hilder VA, Gatehouse AMR, Sheerman SE, Baker RF, Boulter D (1987) A novel mechanism of insect resistance engineered into tobacco. Nature 330:160–163
Hinson K, Nino RH, Boote KJ (1978) Characteristics of removed leaflets and yield response of artificially defoliated soybeans. Soil Crop Sci Soc Fla Proc 37:104–109
Hirasawa T, Tanaka K, Miyamoto D, Takei M, Ishihara K (1994) Effects of pre-flowering moisture deficits on dry matter production and ecophysiological characteristics in soybean plants under drought conditions during grain filling. Jpn J Crop Sci 63:721–730
Ho LC (1979) Regulation of assimilate translocation between leaves and fruits in the tomato. Ann Bot 43:437–448
Ho LC (1984) Partitioning of assimilates in fruiting tomato plants. Plant Growth Regul 2:277–285
Ho LC (1988) Metabolism and compartmentation of imported sugars in sink organs in relation to sink strength. Ann Rev Plant Physiol Plant Mol Biol 39:355–378
Hoeft RG, Nafziger ED, Johnson RR, Aldrich SR (2000) Soybean as a crop. In: Aldrich SR, Nafziger ED, Johnson RR (eds) Modern corn and soybean production. MCSP, Illinois, pp 1–353
Holmstrom KO, Mantyla E, Welin B, Mandal A, Tunnela OE, Londesborough J, Palva ET (1996) Drought tolerance in tobacco. Nature 379:683–684
Holshouser DL (2010) Days to soybean physiological maturity. Virginia Cooperative Extension, Blacksburg, pp 1009–1459
Hou X, Xie K, Yao J, Qi Z, Xiong L (2009) A homolog of human ski-interacting protein in rice positively regulates cell viability and stress tolerance. Proc Natl Acad Sci U S A 106:6410–6415
Hsieh TH, Lee JT, Charng YY, Chan MT (2002) Tomato plants ectopically expressing Arabidopsis CBF1 show enhanced resistance to water deficit stress. Plant Physiol 130:618–626
Hsieh TH, Li CW, Su RC, Cheng CP, Sanjaya S, Tsai YC, Chan MT (2010) A tomato bZIP transcription factor, SlAREB, is involved in water deficit and salt stress response. Planta 231:1459–1473
Hu Y, Xie Q, Nam-Hai C (2003) The Arabidopsis Auxin-Inducible Gene ARGOS controls lateral organ size. Plant Cell 15:1951–1961
Hu Y, Poh HM, Nam-Hai C (2006) The Arabidopsis ARGOS-LIKE gene regulates cell expansion during organ growth. The Plant J 47:1–9
Huang J, Sun SJ, Xu DQ, Yang X, Bao YM, Wang ZF, Tang HJ, Zhang H (2009a) Increased tolerance of rice to cold, drought and oxidative stresses mediated by the overexpression of a gene that encodes the zinc finger protein ZFP245. Biochem Biophys Res Commun 389:556–561
Huang XY, Chao DY, Gao JP, Zhu MZ, Shi M, Lin HX (2009b) A previously unknown zinc finger protein, DST, regulates drought and salt tolerance in rice via stomatal aperture control. Genes Dev 23:1805–1817
Huck MG, Ishihara K, Peterson CM, Ushijima T (1983) Soybean adaptation to water stress at selected stages of growth. Plant Physiol 73:422–427
Huff A, Dybing D (1980) Factors affecting shedding of flowers in soybean (Glycine max (L) Merrill). J Exp Bot 31:751–762
Hufstetler EV, Boerma HR, Carter TE, Earl HG (2007) Genotypic variation for three physiological traits affecting drought tolerance in soybean. Crop Sci 47(25-):35
Hunt TE, Baldin ELL (2012) Soybean insects: ecology and control. In: Cookosn R (ed)Encyclopedia of pest management. (Published online 08 Aug), Taylor and Francis, New York, pp 1–4
Hymowitz T (1970) On domestication of soybean. Econ Bot 24:408–421
Hymowitz T, Newell CA (1981) Taxonomy of the genus Glycine, domestication and uses of soybeans. Econ Bot 35:272–288
Hymowitz T, Shurtleff WR (2005) Debunking soybean myths and legends in the historical and popular literature. Crop Sci 45:473–476
Ihnatowicz A, Pesaresi P, Varotto C, Richly E, Schneider A, Jahns P, Leister D (2004) Mutants for photosystem I subunit D of Arabidopsis thaliana: effects on photosynthesis, photosystem I stability and expression of nuclear genes for chloroplast functions. Plant J 37:839–852
Imaizumi T (2010) Arabidopsis circadian clock and photoperiodism: time to think about location. Curr Opinion Plant Biol 13:83–89
Imaizumi T, Tran HG, Swartz TE, Briggs WR, Kay SA (2003) FKF1 is essential for photoperiodic-specific light signaling in Arabidopsis. Nature 426:302–306
Imsande J (1988) Interrelationship between plant development stage, plant growth rate, nitrate utilization and nitrogen fixation in hydroponically grown soybean. J Exp Bot 39:775–785
Ingram KT, Herzog DC, Boote KJ, Jones JW, Barfield CS (1981) Effects of defoliating pests on soybeans canopy CO2 exchange and reproductive growth. Crop Sci 21:961–968
Ishimaru K, Hirotsu N, Kashiwagi T, Madoka Y, Nagasuga K, Ono K, Ohsugi R (2008) Overexpression of a maize SPS gene improves yield characters of potato under field conditions. Plant Prod Sci 11:104–107
James RF, Carl RC, Philip JB (2001) Drought stress effects on branch and main seed yield and yield components of determinate soybean. Crop Sci 41:759–763
James C (2009) Global status of commercialized biotech/GM crops. The International Service for the Acquisition of Agri-biotech Application (ISAAA) Brief No 41. ISAAA: Ithaca
Jang IC, Oh SJ, Seo JS, Choi WB, Song SI, Kim CH et al (2003) Expression of a bifunctional fusion of the Escherichia coli genes for trehalose-6-phosphate synthase and trehalose-6-phosphate phosphatase in transgenic rice plants increases trehalose accumulation and abiotic stress tolerance without stunting growth. Plant Physiol 131:516–524
Jenner CF (1985) Control of the accumulation of starch and protein in cereal grains. In: Jeffcoat B, Hawkins AF, Stead AD (eds) Regulation of sources and sinks in crop plants. British Plant Growth Regulator Group, Long Ashton, pp 195–209
Jenner CF, Ugalde TD, Aspinall D (1991) The physiology of starch and protein deposition in the endosperm of wheat. Aust J Plant Physiol 18:211–226
Jeong JS, Kim YS, Baek KH, Jung H, Ha SH, Do Choi Y, Kim M, Reuzeau C, Kim JK (2010) Root-specific expression of OsNAC10 improves drought tolerance and grain yield in rice under field drought conditions. Plant Physiol 153:185–197
Ji W, Zhu Y, Li Y, Yang L, Zhao X, Cai H, Bai X (2010) Over-expression of a glutathione S-transferase gene, GsGST, from wild soybean (Glycine soja) enhances drought and salt tolerance in transgenic tobacco. Biotechnol Letts 32:1173–1179
Jones P, Allen LH Jr, Jones JW, Boote KJ, Campbell WJ (1984) Soybean canopy growth, photosynthesis, and transpiration responses to whole-season carbon dioxide enrichment. Agron J 76:633–637
Kadhem FA, Specht JE, Williams JH (1985) Soybean irrigation serially timed during stages R1 to R6 II Yield component responses. Agron J 77:299–304
Kallarackal J, Milburn JA (1984) Specific mass transfer and sink-controlled phloem translocation in castor bean. Austr J Plant Physiol 11:483–490
Kanneganti V, Gupta AK (2008) Overexpression of OsiSAP8, a member of stress associated protein (SAP) gene family of rice confers tolerance to salt, drought and cold stress in transgenic tobacco and rice. Plant Mol Biol 66:445–462
Kaplan SL, Koller HR (1974) Variation among soybean cultivars in seed growth rate during the linear phase of seed growth. Crop Sci 14:613–614
Kar RK (2011) Plant responses to water stress: role of reactive oxygen species. Plant Signal Behav 6:1741–1745
Karim S, Aronsson H, Ericson H, Pirhonen M, Leyman B, Welin B, Mantyla E, Palva ET, Van Dijck P, Holmstrom KO (2007) Improved drought tolerance without undesired side effects in transgenic plants producing trehalose. Plant Mol Biol 64:371–386
Karl TR, Melillo JM, Peterson TC (2009) (eds) Global climate change impacts in the United States. Cambridge University Press, New York, pp 196
Kasuga M, Miura S, Shinozaki K, Yamaguchi-Shinozaki K (2004) A combination of the Arabidopsis DREB1 A gene and stress inducible rd29 A promoter improved drought- and low temperature stress tolerance in tobacco by gene transfer. Plant Cell Physiol 45:346–350
Kavi-Kishor P, Hong Z, Miao GH, Hu C, Verma D (1995) Overexpression of [delta]-pyrroline-5-carboxylate synthetase increases proline production and confers osmotolerance in transgenic plants. Plant Physiol 108:1387–1394
Kebeish R, Niessen M, Thiruveedhi K, Bari R, Hirsch HJ, Rosenkranz R, Stabler N, Schonfeld B, Kreuzaler F, Peterhansel C (2007) Chloroplastic photorespiratory bypass increases photosynthesis and biomass production in Arabidopsis thaliana. Nat Biotech 25:593–599
Keller T, Abbott J, Moritz T, Doernera P (2006) Arabidopsis REGULATOR OF AXILLARY MERISTEMS1 controls a leaf axil stem cell niche and modulates vegetative development. Plant Cell 18:598–611
Kim MH, Sasaki K, Imai R (2009) Cold shock domain Protein 3 regulates freezing tolerance in Arabidopsis thaliana. J Biol Chem 284:23454–23460
Klink VP, Alkharouf N, Macdonald M, Matthews B (2005) Laser capture microdissection (LCM) and expression analyses of Glycine max (soybean) syncytium containing root regions formed by the plant pathogen Heterodera glycines (soybean cyst nematode). Plant Mol Biol 59:965–979
Klink VP, Kim KH, Martins V, Macdonald MH, Beard HS, Alkharouf NW et al (2009) A correlation between host-mediated expression of parasite genes as tandem inverted repeats and abrogation of development of female Heterodera glycines cyst formation during infection of Glycine max. Planta 230:53–71
Kocsy G, Laurie R, Szalai G, Szilagyi V, Simon-Sarkadi L, Galiba G et al (2005) Genetic manipulation of proline levels affects antioxidants in soybean subjected to simultaneous drought and heat stresses. Physiol Plant 124:227–235
Kokubun M, Watanabe K (1983) Analysis of the yield determining process of field grown soybeans in relation to canopy structure VII Effects of source and sink manipulations during reproductive growth on yield and yield components. Japan J Crop Sci 52:215–219
Kokubun M, Shimada S, Takahashi M (2001) Flower abortion caused by pre-anthesis water deficit is not attributed to impairment of pollen in soybean. Crop Sci 4:1517–1521
Kumar A, Li C, Portis AR Jr (2009) Arabidopsis thaliana expressing a thermostable chimeric Rubisco activase exhibits enhanced growth and higher rates of photosynthesis at moderately high temperatures. Photosynth Res 100:143–153
Kunz HH, Hausler RE, Fettke J, Herbst K, Niewiadomski P, Gierth M, Bell K, Steup M, Flugge UI, Schneider A (2010) The role of plastidial glucose-6-phosphate/phosphate translocators in vegetative tissues of Arabidopsis thaliana mutants impaired in starch biosynthesis. Plant Biol 1:115–128
Labate MT, Ko K, Ko ZW, Pinto LS, Real MJ, Romano MR, Barja PR, Granell A, Friso G, van Wijk KJ, Brugnoli E, Labate CA (2004) Constitutive expression of pea Lhcb 1-2 in tobacco affects plant development, morphology and photosynthetic capacity. Plant Mol Biol 55:701–714
Lang A, During H (1991) Partitioning control by water potential gradient: evidence for compartmentation breakdown in grape berries. J Exp Bot 42:1117–1122
Lang A, Thorpe MR (1986) Water potential, translocation and assimilate partitioning. J Exp Bot 37:495–503
Laporte MM, Shen B, Tarczynski MC (2002) Engineering for drought avoidance: expression of maize NADP-malic enzyme in tobacco results in altered stomatal function. J Exp Bot 53:699–705
Layzell DB, LaRue TA (1982) Modeling C and N transport to developing soybean fruits. Plant Physiol 70:1290–1298
Lecardonnel A, Chauvin L, Jouanin L, Beaujean A, Prevost G, Sangwan B (1999) Effects of rice cystatin I expression in transgenic potato on Colorado potato beetle larvae. Plant Sci 140:71–79
Lee SK, Hwang SK, Han M, Eom JS, Kang HG, Han Y, Choi SB, Cho MH, Bhoo SH, An G, Hahn TR, Okita TW, Jeon JS (2007) Identification of the ADP-glucose pyrophosphorylase isoforms essential for starch synthesis in the leaf and seed endosperm of rice (Oryza sativa L). Plant Mol Biol 65:531–546
Lee SK, Jeon JS, Börnke F, Voll L, Cho JI, Goh CH, Jeong SW, Park YI, Kim SJ, Choi SB, Miyao A, Hirochika H, An G, Cho MH, Bhoo SH, Sonnewald U, Hahn TR (2008) Loss of cytosolic fructose-1,6-bisphosphatase limits photosynthetic sucrose synthesis and causes severe growth retardations in rice (Oryza sativa). Plant Cell Env 31:1851–1863
Lefebvre S, Lawson T, Fryer M, Zakhleniuk OV, Lloyd JC, Raines CA (2005) Increased sedoheptulose-1,7-bisphosphatase activity in transgenic tobacco plants stimulates photosynthesis and growth from an early stage in development. Plant Physiol 138:451–460
Leggewie G, Kolbe A, Lemoine R, Roessner U, Lytovchenko A, Zuther E, Kehr J, Frommer W, Riesmeier J, Willmitzer L, Fernie A (2003) Overexpression of the sucrose transporter SoSUT1 in potato results in alterations in leaf carbon partitioning and in tuber metabolism but has little impact on tuber morphology. Planta 217:158–167
Lewis JM, Mackintosh CA, Shin S, Gilding E, Kravchenko S, Baldridge G, Zeyen R, Muehlbauer GL (2008) Overexpression of the maize Teosinte Branched1 gene in wheat suppresses tiller development. Plant Cell Rep 27:1217–1225
Li S, Yin D, Wu F, Wang S, Deng Q, Tang Y, Zhou H, Ping L (2006) Introduction of the PPF1 gene into rice (Oryza sativa L.) results in delayed leaf senescence. Euphytica 153:257–265
Li F, Ma C, Wang X, Gao C, Zhang J, Wang y, Cong N, Li X, Wen J, Yi B, Shen J, Tu J, Fu T (2011a) Characterization of sucrose transporter alleles and their association with seed yield-related traits in Brassica napus L. BMC Plant Biol 11:168–181
Li N, Zhang S, Zhao Y, Li B, Zhang J (2011b) Over-expression of AGPase genes enhances seed weight and starch content in transgenic maize. Planta 233:241–250
Li X, Cheng X, Liu J, Zeng H, Han L, Tang W (2011c) Heterologous expression of the Arabidopsis DREB1 A/CBF3 gene enhances drought and freezing tolerance in transgenic Lolium perenne plants. Plant Biotech Rep 5:61–69
Lian HL, Yu X, Ye Q, Ding X, Kitagawa Y, Kwak SS, Su WA, Tang ZCT (2004) The role of aquaporin RWC3 in drought avoidance in rice. Plant Cell Physiol 45:481–489
Lieman-Hurwitz J, Rachmilevitch S, Mittler R, Marcus Y, Kaplan A (2003) Enhanced photosynthesis and growth of transgenic plants that express ictB, a gene involved in HCO3—accumulation in cyanobacteria. Plant Biotech J 1:43–50
Lilley CJ, Goodchild SA, Atkinson HJ, Urwin PE (2005) Cloning and characterization of a Heterodera glycines aminopeptidase cDNA. Int J Parasitol 35:1577–1585
Liu F, Andersen MN, Jensen CR (2003) Loss of pod set caused by drought stress is associated with water status and ABA content of reproductive structures in soybean. Funct Plant Biol 30:271–280
Liu W, Wu C, Fu Y, Hu G, Si H, Zhu L, Luan W, He Z, Sun Z (2009a) Identification and characterization of HTD2:a novel gene negatively regulating tiller bud outgrowth in rice. Planta 230:649–658
Liu WY, Wang MM, Huang J, Tang HJ, Lan HX, Zhang HS (2009b) The OsDHODH1 gene is involved in salt and drought tolerance in rice. J Int Plant Biol 51:825–833
Liu B, Xiao-Bing L, Wang C, Yan-Sheng L, Jin J, Herbert SJ (2010) Long distance transport of assimilates is shown to exist in soybean plants. African J Agric Res 5:551–554
Long SP, Ainsworth EA, Leakey ADB, Nosberger J, Ort DR (2006a) Food for thought: lower-than-expected crop yield stimulation with rising CO2 concentrations. Sci 312:1918–1921
Long SP, Xin-Guang Z, Naidu SL, Ort DR (2006b) Can improvement in photosynthesis increase crop yields? Plant Cell Environ 29:315–330
Lu G, Gao C, Zheng X, Han B (2009) Identification of OsbZIP72 as a positive regulator of ABA response and drought tolerance in rice. Planta 229:605–615
Luedders VD (1977) Genetic improvement in yield of soybeans. Crop Sci 17:971–972
Luo M, Dennis ES, Berger F, Peacock WJ, Chaudhury A (2005) MINISEED3 (MINI3), a WRKY family gene, and HAIKU2 (IKU2), a leucine rich repeat (LRR) KINASE gene, are regulators of seed size in Arabidopsis. Proc Natl Acad Sci U S A 102:17531–17536
Lv SL, Lian LJ, Tao PL, Li ZX, Zhang KW, Zhang JR (2009) Overexpression of Thellungiella halophila H+ -PPase (TsVP) in cotton enhances drought stress resistance of plants. Planta 229:899–910
Lytovchenko A, Schauer N, Willmitzer L, Fernie AR (2005) Tuber-specific cytosolic expression of a bacterial phosphoglucomutase in potato (Solanum tuberosum L) dramatically alters carbon partitioning. Plant Cell Physiol 46:588–597
Ma Y, Baker RF, Magallanes-Lundback M, DellaPenna D, Braun DM (2008) Tie-dyed1 and sucrose export defective1 act independently to promote carbohydrate export from maize leaves. Planta 227:527–538
MacRae TC, Baur ME, Boethel DJ, Fitzpatrick BJ, Gao AG, Gamundi JC et al (2005) Laboratory and field evaluations of transgenic soybean exhibiting high dose expression of a synthetic Bacillus thuringiensis cry1 A gene for control of Lepidoptera. J Econ Entomol 98:577–587
Major DJ, Johnson DR, Tanner JW, Anderson IC (1975) Effects of daylength and temperature on soybean development. Crop Sci 15:174–179
Mallikarjuna G, Mallikarjuna K, Reddy M, Kaul T (2011) Expression of OsDREB2 A transcription factor confers enhanced dehydration and salt stress tolerance in rice (Oryza sativa L). Biotechnol Letts 33:1689–1697
Manavalan LP, Chen X, Clarke J, Salmeron J, Nguyen HT (2012) RNAi-mediated disruption of squalene synthase improves drought tolerance and yield in rice. J Exp Bot 63:163–175
Maqbool B, Zhong H, El-Maghraby Y, Ahmad A, Chai B, Wang W, Sabzikar R, Sticklen B (2002) Competence of oat (Avena sativa L) shoot apical meristems for integrative transformation, inherited expression, and osmotic tolerance of transgenic lines containing hva1. Theor Appl Genet 105:201–208
Marcelis LFM (1996) Sink strength as a determinant of dry matter partitioning in the whole plant. J Exp Bot 47:1281–1291
Masumoto C, Shin-Ichi M, Ohkawa H, Fukuda T, Taniguchi Y, Murayama S, Kusano M, Saito K, Fukayama H, Miyao M (2010) Phosphoenolpyruvate carboxylase intrinsically located in the chloroplast of rice plays a crucial role in ammonium assimilation. Proc Natl Acad Sci U S A 107:5226–5531
Matsukura S, Mizoi J, Yoshida T, Todaka D, Ito Y, Maruyama K, Shinozaki K, Yamaguchi-Shinozaki K (2010) Comprehensive analysis of rice DREB2-type genes that encode transcription factors involved in the expression of abiotic stress-responsive genes. Mol Genet Gent 283:185–196
McAlister DF, Krober OA (1958) Response of soybean to leaf and pod removal. Agron J 50:674–677
McKersie BD, Bowley SR, Harjanto E, Leprince O 1996) Water deficit tolerance and field performance of transgenic Alfalfa overexpressing Superoxide Dismutase. Plant Physiol 111:1177–1181
Mcpherson RM, Macrae TC (2009) Evaluation of transgenic soybean exhibiting high expression of a synthetic Bacillus thuringiensis cry1 A transgene for suppressing lepidopteran population densities and crop injury. J Econ Entomol 102:1640–1648
McWilliams DA, Berglund DR, Endres GJ (2004) Soybean growth and management: quick guide. North Dakota State University Extension Service, Fargo, pp 8
Melis A (2009) Solar energy conversion efficiencies in photosynthesis: minimizing the chlorophyll antennae to maximize efficiency. Plant Sci 17:272–280
Meng Z, Barg R, Yin M, Gueta-Dahan Y, Leikin-Frenkel A, Salts Y, Shabtai S, Ben-Hayyim G (2005) Modulated fatty acid desaturation via overexpression of two distinct omega-3 desaturases differentially alters tolerance to various abiotic stresses in transgenic tobacco cells and plants. Plant J 44:361–371
Meyer S, Melzer M, Tuernit E, Hummer C, Besenbeck R, Stadler R, Sauer N (2000) AtSUC3, a gene encoding a new Arabidopsis sucrose transporter is expressed in cells adjacent to the vascular tissue and in a carpel cell layer. Plant J 24:869–882
Mian MAR, Mailey MA, Ashley DA, Wells R, Carter TE, Parrot WA et al (1996) Molecular markers associated with water use efficiency and leaf ash in soybean. Crop Sci 36:1252–1257
Miklos JA, Alibhai MF, Bledig SA, Connor-Ward DC, Gao AG, Holmes BA et al (2007) Characterization of soybean exhibiting high expression of a synthetic Bacillus thuringiensis cry1 A transgene that confers a high degree of resistance to lepidopteran pests. Crop Sci 47:148–157
Mishra M, Mahajan N, Tamhane VA, Kulkarni MJ, Baldwin IT, Gupta VS, Giri AP (2012) Stress inducible proteinase inhibitor diversity in Capsicum annuum. BMC Plant Biol 12(217):14
Mittler R (2006) Abiotic stress, the field environment and stress combination. Trends Plant Sci 11:15–19
Mittler R, Blumwald E (2010) Genetic engineering for modern agriculture: challenges and perspectives. Ann Rev Plant Biol 61:443–462
Mittler R, Vanderauwera S, Gollery M, Van Breusegem F (2004) Reactive oxygen gene network of plants. Trends Plant Sci 9:490–497
Mizoguchi T, Wright L, Fujiwara S, Cremer F, Lee K, Onouchi H, Mouradov A, Fowler S, Kamada H, Putterill J et al (2005) Distinct roles of GIGANTEA in promoting flowering and regulating circadian rhythms in Arabidopsis. Plant Cell 17:2255–2270
Mizoi J, Shinozaki K, Yamaguchi-Shinozaki K (2012) AP2/ERF family transcription factors in plant abiotic stress responses. Biochim Biophys Acta 1819:86–96
Morran S, Eini O, Pyvovarenko T, Parent B, Singh R, Ismagul A, Eliby S, Shirley N, Langridge P, Lopato S (2011) Improvement of stress tolerance of wheat and barley by modulation of expression of DREB/CBF factors. Plant Biotech J 9:230–249
Morrison MJ, Voldeng HD, Cober ER (2000) Physiological changes from fifty-eight years of genetic improvement of short-season cultivars in Canada. Agron J 92:780–784
Mueller TA, Miles MR, Morel W, Marios JJ, Wright DL, Kemerait RC et al (2009) Effect of fungicide and timing of application on soybean rust severity and yield. Plant Dis 93:243–248
Munier-Jolain NG, Munier-Jolain NM, Roche R, Ney B, Duthion C (1998) Seed growth rate in grain legumes I: effect of photoassimilate availability on seed growth rate. J Exp Bot 49:1963–1969
Munoz-Bertomeu J, Cascales-Minana B, Mulet JM, Baroja-Fernandez E, Pozueta-Romero J, Kuhn JM, Segura J, Ros R (2009) Plastidial glyceraldehyde-3-phosphate dehydrogenase deficiency leads to altered root development and affects the sugar and amino acid balance in Arabidopsis. Plant Physiol 151:541–558
Murchie EH, Sarrobert C, Contard P, Betsche T, Foyer CH, Galtier N (1999) Overexpression of sucrose phosphate synthase in tomato plants grown with carbondioxide enrichment leads to decreased foliar carbohydrate accumulation relative to untransformed controls. Plant Physiol Biochem 37:251–260
Na-Gyong L, Stein B, Suzuki H, Verma DS (1993) Expression of antisense nodulin-35 RNA in Vigna aconitifolia transgenic root nodules retards peroxisome development and affects nitrogen availability to the plant. Plant J 3:599–606
Nakagawa H, Chang-Jie J, Sakakibara H, Kojima M, Honda I, Ajisaka H, Nishijima T, Koshioka M, Homma T, Mander LN, Takatsuji H (2005) Overexpression of a petunia zinc-finger gene alters cytokinin metabolism and plant forms. Plant J 41:512–523
Nakamoto H, Hasegawa M (1999) Targeted Inactivation of the gene psaK encoding a subunit of photosystem I from the cyanobacterium, Synechocystis sp PCC 6803. Plant Cell Physiol 40:9–16
Nakamoto H, Shao-Hui Z, Tanaka K, Yamazaki A, Furuya T, Iwaya-Inoue M, Fukuyama M (2004) Effects of carbon dioxide enrichment during different growth periods on flowering, pod set and seed yield in soybean. Plant Prod Sci 7(1):11–15
Niblack TL, Chen S (2004) Cropping systems. In: Schmitt DP, Wrather JA, Riggs RD (eds) Biology and management of the soybean cyst nematode, 2nd edn. Schmitt and Associates, Marceline, pp 181–206
Niittyla T, Messerli G, Trevisan M, Chen J, Smith AM, Zeeman SC (2004) A preciously unknown maltose transporter essential for starch degradation in leaves. Science 303:87–89
Ning Y, Jantasuriyarat C, Zhao Q, Zhang H, Chen S, Liu J, Liu L, Tang S, Park CH, Wang X et al (2011) The SINA E3 ligase OsDIS1 negatively regulates drought response in rice. Plant Physiol 157:242–255
Nunes-Nesi A, Fernie AR, Stitt M (2010) Metabolic and signaling aspects underpinning the regulation of plant carbon nitrogen interactions. Mol Plant 3:973–996
Obana Y, Omoto D, Kato C, Matsumoto K, Nagai Y, Kavakli H et al (2006) Enhanced turnover of transitory starch by expression of up-regulated ADP-glucose pyrophosphorylases in Arabidopsis thaliana. Plant Sci 170:1–11
Oberschall A, Deak M, Torok K, Saa L, Vass I, Kovacs I et al (2000) A novel aldose/aldehyde reductase protects transgenic plants against lipid peroxidation under chemical and drought stresses. Plant J 24:437–446
Oh SJ, Song SI, Kim YS, Jang HJ, Kim SY, Kim M et al (2005) Arabidopsis CBF3/DREB1 A and ABF3 in transgenic rice increased tolerance to abiotic stress without stunting growth. Plant Physiol 138:341–351
Oh SJ, Kim YS, Kwon CW, Park HK, Jeong JS, Kim JK (2009) Overexpression of the transcription factor AP37 in rice improves grain yield under drought conditions. Plant Physiol 150:1368–1379
Ohyama T, Kawai S (1982) Nitrogen assimilation and transport in soybean leaves: investigation by petiole girdling treatment. Soil Sci Nutr 29:227–231
Okita TW, Sun J, Sakulringharoj C, Choi SB, Edwards GE, Kato C, Ito H, Matsui H (2001) Increasing rice productivity and yield by manipulation of starch synthesis. Novartis Found Symp 236:135–146
Ort DR, Zhu XG, Melis A (2011) Optimizing antenna size to maximize photosynthetic efficiency. Plant Physiol 155:79–85
Park JY, Canam T, Kyu-Young K, Ellise DD, Mansfield SD (2008) Over-expression of an Arabidopsis family A sucrose phosphate synthase (SPS) gene alters plant growth and fibre development. Trans Res 17:181–192
Park GG, Park JJ, Yoon J, Yu SN, An GA (2010) RING finger E3 ligase gene, Oryza sativa Delayed Seed Germination 1 (OsDSG1), controls seed germination and stress responses in rice. Plant Mol Biol 74:467–478
Parry MAJ, Madgwick PJ, Carvalho JFC, Andralojc PJ (2007) Prospects for increasing photosynthesis by overcoming the limitations of Rubisco. J Agric Sci 145:31–43
Pasapula V, Shen G, Kuppu S, Paez-Valencia J, Mendoza M, Hou P, Chen J, Qiu X, Zhu L, Zhang X et al (2011) Expression of an Arabidopsis vacuolar H+ -pyrophosphatase gene (AVP1) in cotton improves drought- and salt tolerance and increases fibre yield in the field conditions. Plant Biotech J 9:88–99
Pate and coworkers (1977) Nutrition of a developing legume fruit. Plant Physiol 59:506–510
Patrick JW (1988) Assimilate partitioning in relation to crop productivity. Hort Sci 23:33–40
Patrick JW (1997) Phloem unloading: sieve element unloading and post-sieve element transport. Ann Rev Plant Physiol Plant Mol Biol 48:191–222
Patten KD, Patterson ME, Proebsting EL (1986) Factors accounting for the within-tree variation of fruit quality in sweet cherries. J Amer Soc Hort Sci 111:356–360
Paul C, Hartman GL (2009) Sources of soybean rust resistance challenged with single-spored isolates of Phakopsora pachyrhizi collected from the USA. Crop Sci 49:1781–1785
Pedersen P (2008) Weed management matters in soybean. Iowa Soybean Review, Iowa Soybean Association, Spring:13. extension.agron.iastate.edu/soybean/aboutus_techpubs2.html.
Pedersen P, Kumudini S, Board J, Conley S (2007) Soybean growth and development. In: Dorrance AE (ed) Using foliar fungicides to manage soybean rust. Dep. of Plant Pathology Extension Publication, The Ohio State University, Columbus, pp 41–47
Peet MM, Kramer PJ (1980) Effects of decreasing source/sink ratio in soybeans on photosynthesis, photorespiration, transpiration and yield. Plant Cell Env 3:201–206
Peleg Z, Reguera M, Tumimbang E, Walia H, Blumwald E (2011) Cytokinin-mediated source/sink modifications improve drought tolerance and increase grain yield in rice under water-stress. Plant Biotech J 9:747–758
Pelissier HC, Frerich A, Desimone M, Schumacher K, Tegeder M (2004) PvUPS1, an allantoin transporter in nodulated roots of French bean. Plant Physiol 134:664–675
Pellegrineschi A, Reynolds M, Pacheco M, Brito RM, Almeraya R, Yamaguchi-Shinozaki K, Hoisington D (2004) Stress-induced expression in wheat of the Arabidopsis thaliana DREB1 A gene delays water stress symptoms under greenhouse conditions. Genome 47:493–500
Peterhansel C, Niessen M, Kebeish R (2008) Metabolic engineering towards the enhancement of photosynthesis. Photochem Photobiol 84:1317–1321
Pham TA, Miles MR, Frederick RD, Hill CB, Hartman GL (2009) Differential responses of resistant soybean genotypes to ten isolates of Phakopsora pachyrhizi. Plant Dis 93:224–228
Pickle CS, Caviness CE (1984) Yield reduction from defoliation and plant cut-off of determinate and semi-determinate soybean. Agron J 76:474–476
Pilon-Smits EAH, Terry N, Sears T, Kim H, Zayed A, Hwang S, van Dun K, Voogd E, Verwoerd TC, Krutwagen RWHH, Goddijn OJM (1998) Trehalose-producing transgenic tobacco plants show improved growth performance under drought stress. J Plant Physiol 152:525–532
Pilon-Smits EAH, Terry N, Sears T, van Dun K (1999) Enhanced drought resistance in fructan-producing sugar beet. Plant Physiol Biochem 37:313–317
Preuss SB, Meister R, Xu Z, Urwin CP, Tripodi FA, Screen SE, Anil VS, Zhu Z, Morrell JA, Liu G, Ratcliffe OJ, Reuber TL, Khanna R, Goldman BS, Bell E, Ziegler TE, McClerren AL, Ruff TG, Petracek ME (2012) Expression of the Arabidopsis thaliana BBX32 Gene in Soybean Increases Grain Yield. PLoS ONE 7:e30717
Purcell LC, Specht JE (2004) Physiological traits for ameliorating drought stress. In: Specht JE, Boema HR (eds) Soybeans: improvement, production, and uses. Agronomy monographs, 3rd edn. ASA, Madison, pp 569–620
Quan R, Hu S, Zhang Z, Zhang H, Zhang Z, Huang R (2010) Overexpression of an ERF transcription factor TSRF1 improves rice drought tolerance. Plant Biotech J 8:476–488
Que Q, Chilton MDM, de Fontes CM, He C, Nuccio M, Zhu T, Wu Y, Chen JS, Shi L (2010) Trait stacking in transgenic crops: Challenges and opportunities. GM Crops 1:220–229
Rainbird RM, Thorne JH, Hardy RW (1984) Role of amides, amino acids, and ureides in the nutrition of developing soybean seeds. Plant Physiol 74:329–334
Raper CD, Kramer PJ (1987) Stress physiology. In: Wilcox JR (ed) Soybeans: improvement, production, and uses, 2nd edn. ASA, Madison, pp 589–641
Rentsch D, Schmidt S, Tegeder M (2007) Transporters for uptake and allocation of organic nitrogen compounds in plants. FEBS Lett 581:2281–2289
Rizhsky L, Liang H, Mittler R (2002) The combined effect of drought stress and heat shock on gene expression in tobacco. Plant Physiol 130:1143–1151
Rizhsky L, Liang H, Mittler R (2003) The water-water cycle is essential for chloroplast protection in the absence of stress. J Biol Chem 278:38921–38925
Rizhsky L, Liang H, Shuman J, Shulaev V, Davletova S, Mittler R (2004) When defense pathways collide the response of Arabidopsis to a combination of drought and heat stress. Plant Physiol 134:1683–1696
Robson PRH, McCormac AC, Irvine AS, Smith H (1996) Genetic engineering of harvest index in tobacco through overexpression of a phytochrome gene. Nat Biotechnol 14:995–998
Rogers HH, Cure JD, Thomas JF, Smith JM (1984) Influence of elevated CO2 on growth of soybean plants. Crop Sci 24:361–366
Rolletschek H, Borisjuk L, Radchuk R, Miranda M, Heim U, Wobus U, Weber H (2004) Seed-specific expression of a bacterial phosphoenolpyruvate carboxylase in Vicia narbonensis increases protein content and improves carbon economy. Plant Biotech J 2:211–219
Rolletschek H, Nguyen TH, Hausler RE, Rutten T, Gobel C, Feussner I, Radchuk R, Tewes A, Claus B, Klukas C, Linemann U, Weber H, Wobus U, Borisjuk L (2007) Antisense inhibition of the plastidial glucose-6-phosphate/phosphate translocator in Vicia seeds shifts cellular differentiation and promotes protein storage. Plant J 51:468–484
Rontein D, Basset G, Hanson AD (2002) Metabolic engineering of osmoprotectant accumulation in plants. Metab Eng 4:49–56
Rosche E, Blackmore D, Tegeder M, Richardson T, Schroeder H, Higgins TJV, Frommer WB, Offler CE, Patrick JW (2002) Seed-specific overexpression of a potato sucrose transporter increases sucrose uptake and growth rates of developing pea cotyledons. Plant J 30:165–175
Rosche EG, Blackmore D, Offler CE, Patrick JW (2005) Increased capacity for sucrose uptake leads to earlier onset of protein accumulation in developing pea seeds. Func Plant Biol 32:997–1007
Rosenthal DM, Locke AM, Khozaei M, Raines CA, Long SP, Ort DR (2011) Over-expressing the C3 photosynthesis cycle enzyme sedoheptulose-1-7 bisphosphatase improves photosynthetic carbon gain and yield under fully open air CO2 fumigation (FACE). BMC Plant Biol 11:123–134
Roy M, Wu R (2001) Arginine decarboxylase transgene expression and analysis of environmental stress tolerance in transgenic rice. Plant Sci 160:869–875
Sahrawy M, Avila C, Chueca A, Canovas FM, Lopez-Gorge J (2004) Increased sucrose level and altered nitrogen metabolism in Arabidopsis thaliana transgenic plants expressing antisense chloroplastic fructose-1,6-bisphosphatase. J Exp Bot 55:2495–2503
Saijo Y, Hata S, Kyozuka J, Shimamoto K, Izui K (2000) Over-expression of a single Ca2+ -dependent protein kinase confers both cold and salt/drought tolerance on rice plants. Plant J 23:319–327
Sakuma Y, Liu Q, Dubouzet JG, Abe H, Shinozaki K, Yamaguchi-Shinozaki K (2002) DNA-binding specificity of the ERF/AP2 domain of Arabidopsis DREBs, transcription factors involved in dehydration and cold inducible gene expression. Biochem Biophys Res Commun 290:998–1009
Sakuma Y, Maruyama K, Qin F, Osakabe Y, Shinozaki K, Yamaguchi-Shinozaki K (2006) Dual function of an Arabidopsis transcription factor DREB2 A in water-stress-responsive and heat-stress-responsive gene expression. Proc Natl Acad Sci U S A 103:18822–18827
Sanders A, Collier R, Tretheway A, Gould G, Sieker R, Tegeder M (2009) AAP1 regulated import of amino acids into developing Arabidopsis embryos. Plant J 59:540–552
Satyendra R, Stewart JM, Wilkins T (1998) Assessment of resistance of cotton transformed with lectin genes to tobacco budworm. Special Report Arkansas Agricultural Experiment Station, Fayetteville, USA, No 188, pp 95–98
Schaik PH, Probst AH (1958) The inheritance of inflorescence type, peduncle length, flower per node and percent flower shedding in soybeans. Agron J 50:98–102
Schmidt A, Su YH, Kunze R, Warner S, Hewitt M, Slocum RD, Ludewig U, Frommer WB, Desimone M (2004) UPS1 and UPS2 from Arabidopsis mediate high affinity transport of uracil and 5-fluorouracil. J Biol Chem 279:44817–44824
Schmidt A, Baumann R, Schwarzkopf A, Frommer WB, Desimone M (2006) Comparative studies on ureide permeases in Arabidopsis thaliana and analysis of two alternative splice variants of AtUPS5. Planta 22:1329–1340
Schmitt DP, Barker KR, Riggs RD (2004) Potential means of management. In: Schmitt DP, Wrather JA, Riggs RD (eds) Biology and management of soybean cyst nematode, 2nd edn. Schmitt and Associates, Marceline, pp 57–72
Schou JB, Jeffers DL, Streeter JG (1978) Effects of reflectors, black boards, or shades applied at different stages of plant development on yield of soybeans. Crop Sci 18:29–34
Schubert KR (1981) Enzymes of purine biosynthesis and catabolism in Glycine max I Comparison of activities with N2 fixation and composition of xylem exudate during nodule development. Plant Physiol 68:1115–1122
Scofield GN, Aoki N, Hirose T, Takano M, Jenkins CL, Furbank RT (2007) The role of the sucrose transporter, OsSUT1, in germination and early seedling growth and development of rice plants. J Exp Bot 58:483–495
Seo JS, Joo J, Kim MJ, Kim YK, Nahm BH, Song SI, Cheong JJ, Lee JS, Kim JK, Do Choi Y (2011) OsbHLH148, a basic helix-loop-helix protein, interacts with OsJAZ proteins in a jasmonate signaling pathway leading to drought tolerance in rice. Plant J 65:907–921
Shan J, Zhu MZ, Shi M, Gao JP, Lin HX (2009) Fine mapping and candidate gene analysis of spd6, responsible for small panicle and dwarfness in wild rice (Oryza rufipogon Griff). Theor Appl Gen 119:827–836
Sharma HC, Sharma KK, Seetharama N, Ortiz R (2000) Prospects for using transgenic resistance to insects in crop improvement. Electronic J Biotech 3:1–20
Shaw RH, Laing DR (1966) Moisture stress and plant response. In: Pierre WH, Kirkham D, Pesek J, Shaw RH (eds) Plant environment and efficient water use. American Society of Agronomy, Madison, pp 73–94
Sheveleva E, Chmara W, Bohnert HJ, Jensen RG (1997) Increased salt and drought tolerance by D-ononitol production in transgenic Nicotiana tabacum L. Plant Physiol 115:1211–1219
Shibles RM, Anderson IC, Gibson AH (1975) Soybean. In: Evans LT (ed) Crop physiology. Cambridge University Press, London, pp 151–190
Shibles RM, Secor J, Ford DM (1987) Carbon assimilation and metabolism. In: Wilcox JR (Ed) Soybeans: improvement, production and uses, 2nd edn. ASA, Madison, pp 535–588
Shinozaki K, Yamaguchi-Shinozaki K (1997) Gene expression and signal transduction in water-stress response. Plant Physiol 115:327–334
Shou H, Bordallo P, Wang K (2004) Expression of the Nicotiana protein kinase (NPK1) enhanced drought tolerance in transgenic maize. J Exp Bot 55:1013–1019
Shou-Min X, Brill E, llewellyn DJ, Furbank RT, Yong-Ling R (2012) Overexpression of a potato sucrose synthase gene in cotton accelerates leaf expansion, reduces seed abortion, and enhances fiber production. Mol Plant 5:430–441
Shpak ED, Lakeman MB, Torii KU (2003) Dominant-Negative receptor uncovers redundancy in the Arabidopsis ERECTA leucine-rich repeat receptor-like kinase signaling pathway that regulates organ shape. Plant Cell 15:1095–1110
Shrawat AK, Carroll RT, DePauw M, Taylor GJ, Good AG (2008) Genetic engineering of improved nitrogen use efficiency in rice by the tissue specific expression of alanine aminotransferase. Plant Biotech J 6:722–732
Shukla RK, Raha S, Tripathi V, Chattopadhyay D (2006) Expression of CAP2, an APETALA2-family transcription factor from chickpea, enhances growth and tolerance to dehydration and salt stress in transgenic tobacco. Plant Physiol 142:113–123
Siefritz F, Tyree MT, Lovisolo C, Schubert A, Kaldenhoff R (2002) PIP1 plasma membrane aquaporins in tobacco: from cellular effects to function in plants. Plant Cell 14:869–876
Sinclair TR, Serraj R (1995) Legume nitrogen fixation and drought. Nature 378:344
Sinclair TR, Purcell LC, King CA, Sneller CH, Chen P, Vadez V (2007) Drought tolerance and yield increase of soybean resulting from improved symbiotic N2 fixation. Field Crops Res 107:68–71
Sindhu AS, Maier TR, Mitchum MG, Hussey RS, Davis EL, Baum TJ (2009) Effective and specific in planta RNAi in cyst nematodes: expression interference of four parasitism genes reduces parasitic success. J Exp Bot 60:315–324
Singh RJ, Hymowitz T (1999) Soybean genetic resources and crop improvement. Genome 42:605–616
Sivamani E, Bahieldin A, Wraith JM, Al-Niemi T, Dyer WE, Ho TD, Qu RI (2000) Improved biomass productivity and water use efficiency under water deficit conditions in transgenic wheat constitutively expressing the barley HVA1 gene. Plant Sci 155:1–9
Sivitz AB, Reinders A, Johnson ME, Krentz AD, Grof PLC, Perroux JM, Ward JM (2006) Arabidopsis sucrose transporter AtSUC9, high-affinity transport activity, intragenic control of expression and early flowering mutant phenotype. Plant Physiol 143:188–198
Smidansky ED, Clancy M, Meyer FD, Lanning SP, Blake NK, Talbert LE, Giroux MJ (2002) Enhanced ADP-glucose pyrophosphorylase activity in wheat endosperm increases seed yield. Proc Natl Acad Sci U S A 99:1724–1729
Smidansky ED, Martin JM, Hannah CL, Fischer AM, Giroux MJ (2003) Seed yield and plant biomass increases in rice are conferred by deregulation of endosperm ADP-glucose pyrophosphorylase. Planta 216:656–664
Smidansky ED, Meyer FD, Blakeslee B, Weglarz TE, Greene TW, Giroux MJ (2007) Expression of a modified ADP-glucose pyrophosphorylase large subunit in wheat seeds stimulates photosynthesis and carbon metabolism. Planta 225:965–976
Smith PMC, Atkins CA (2002) Purine biosynthesis: big in cell division, even bigger in nitrogen assimilation. Plant Physiol 128:793–802
Smith PM, Winter H, Storer PJ, Bussell JD, Schuller KA, Atkins CA (2002) Effect of short-term N2 deficiency on expression of the ureide pathway in cowpea root nodules. Plant Physiol 129:1216–1221
Song YH, Ito S, Imaizumi T (2010) Similarities in the circadian clock and photoperiodism in plants. Curr Opin Plant Biol 13:594–603
Song SY, Chen Y, Chen J, Dai XY, Zhang WH (2011) Physiological mechanisms underlying OsNAC5-dependent tolerance of rice plants to abiotic stress. Planta 234:331–345
Sonnewald U, Mohammad Reza H, Kossmann J, Heyer A, Trethewey RN, Willmitzer L (1997) Increased potato tuber size resulting from apoplastic expression of a yeast invertase. Nat Biotechnol 15:794–797
Sorefan K (2003) MAX4 and RMS1 are orthologous dioxygenase-like genes that regulate shoot branching in Arabidopsis and pea. Genes Dev 17:1469–1474
Soria-Guerra R, Rosales-Mendoza S, Chang S, Haudenshield JS, Padmanaban A, Rodriguez-Zas S et al (2010) Transcriptome analysis of resistant and susceptible genotypes of Glycine tomentella during Phakopsora pachyrhizi infection reveals novel rust resistance genes. Theor Appl Genet 120:1315–1333
Specht JE, Williams JH (1984) Contribution of genetic technology to soybean productivity—retrospect and prospect. In: Fehr WR (ed) Genetic contributions of yield gains of five major crop plants. CSSA, Wisconsin, pp 49–74 (Chapter 3)
Specht JE, Williams JH, Pearson DR (1985) Near-isogenic analyses of soybean pubescence genes. Crop Sci 25:92–96
Specht JE, Hume DJ, Kumudini SV (1999) Soybean yield potential—a genetic and physiological perspective. Crop Sci 39:1560–1570
Spollen WG, Wiebold WJ, Glenn DS (1986) Intra-raceme competition in field-grown soybean. Agron J 78:280–283
Spreitzer RJ, Salvucci ME (2002) Rubisco: structure, regulatory interactions and possibilities for a better enzyme. Ann Rev Plant Biol 53:449–475
Staswick PE (1989) Developmental regulation and the influence of plant sinks on vegetative storage protein gene expression in soybean leaves. Plant Physiol 89:309–315
Steeves RM, Todd TC, Essig JS, Trick HN (2006) Transgenic soybeans expressing siRNAs specific to a major sperm protein gene suppress Heterodera glycines reproduction. Funct Plant Biol 33:991–999
Streeter JG, Jeffers DL (1979) Distribution of total nonstructural carbohydrates in soybean plants having increased reproductive load. Crop Sci 19:729–234
Stewart CN, Adang MJ, All JN, Boerma HR, Cardineau G, Tucker D et al (1996) Genetic transformation, recovery and characterization of fertile soybean transgenic for a synthetic Bacillus thuringiensis cryIAc gene. Plant Physiol 112:121–129
Sugano S, Kaminaka H, Rybka Z, Catala R, Salinas J, Matsui K, Ohme-Takagi M, Takatsuji H (2003) Stress-responsive zinc finger gene ZPT2-3 plays a role in drought tolerance in petunia. Plant J 36:830–841
Sun J, Zhang J, Larue C, Huber SC (2011) Decrease in leaf sucrose synthesis leads to increased leaf starch turnover and decreased RuBP regeneration-limited photosynthesis but not Rubisco-limited photosynthesis in Arabidopsis null mutants of SPSA1. Plant Cell Env 34:592–604
Suzuki Y, Miyamoto T, Yoshizawa R, Mae T, Makino A (2009) Rubisco content and photosynthesis of leaves at different positions in transgenic rice with an overexpression of RBCS. Plant Cell Env 32:417–427
Swiatek M, Kuras R, Sokolenko A, Higgs D, Olive J, Cinque G, Müller B, Eichacker LA, Stern DB, Bassi R, Herrmann RG, Francis-André W (2001) The chloroplast gene ycf9 encodes a photosystem II (PSII) core subunit, PsbZ, that participates in PSII supramolecular architecture. Plant Cell 13:1347–1367
Takasaki H, Maruyama K, Kidokoro S, Ito Y, Fujita Y, Shinozaki K, Yamaguchi-Shinozaki K, Nakashima K (2010) The abiotic stress-responsive NAC-type transcription factor OsNAC5 regulates stress-inducible genes and stress tolerance in rice. Mol Genet Gen 284:173–183
Tamoi M, Nagaoka M, Miyagawa Y, Shigeoka S (2006) Contribution of Fructose-1,6-bisphosphatase and Sedoheptulose-1,7-bisphosphatase to the photosynthetic rate and carbon flow in the Calvin Cycle in transgenic plants. Plant Cell Physiol 47:380–390
Tarantino D, Vannini C, Bracale M, Campa M, Soave C, Murgia I (2005) Antisense reduction of thylakoidal ascorbate peroxidase in Arabidopsis enhances paraquat-induced photooxidative stress and nitric oxide induced cell death. Planta 221:757–765
Thiele A, Herold M, Lenk I, Quail PH, Gatz C (1999) Heterologous expression of Arabidopsis phytochrome B in transgenic potato influences photosynthetic performance and tuber development. Plant Physiol 120:73–82
Thipyapong P, Hunt MD, Steffens JC (2004) Antisense downregulation of polyphenol oxidase results in enhanced disease susceptibility. Planta 220:105–117
Thompson JF, Madison JT, Muenster AE (1977) In vitro culture of immature cotyledons of soya bean (Glycine max L Merrill). Ann Bot 41:29–39
Thorne JH (1985) Phloem unloading of C and N assimilates in developing seeds. Ann Rev Plant Physiol 36:317–343
Tian H, Ma L, Zhao C, Hao H, Gong B, Yu X, Wang X (2010) Antisense repression of sucrose phosphate synthase in transgenic muskmelon alters plant growth and fruit development. Biochem Biophys Res Commun 393:365–370
Todd JW, Morgan LW (1972) Effect of hand defoliation on yield and seed weight of soybeans. J Econ Ent Lanham 65:567–570
Tran LS, Mochida K (2010) Functional genomics of soybean for improvement of productivity in adverse conditions. Funct Integr Genomics 10:447–462
Trujillo LE, Sotolongo M, Menéndez C, Ochogavia ME, Coll Y, Hernández I et al (2008) SodERF3, a novel sugarcane ethylene responsive factor (ERF), enhances salt and drought tolerance when overexpressed in tobacco plants. Plant Cell Physiol 49:512–525
Turner NC, Wright GC, Siddique KHM (2001) Adaptation of grain legumes (pulses) to water limited environments. Adv Agron 71:193–123
Turnipseed SG (1972) Response of soybeans to foliage losses in South Carolina. J Econ Ent Lanham 65:224–229
Udvardi M, Poole PS (2013) Transport and metabolism in legume-rhizobia symbioses. Annu Rev Plant Biol 64:781–805
Uematsu K, Suzuki N, Iwamae T, Inui M, Yukawa H (2012a) Expression of Arabidopsis plastidial phosphoglucomutase in tobacco stimulates photosynthetic carbon flow into starch synthesis. J Plant Physiol 169:1454–1462
Uematsu K, Suzuki N, Iwamae T, Inui M, Yukawa H (2012b) Increased fructose 1,6 bisphosphate aldolase in plastids enhances growth and photosynthesis of tobacco plants. J Exp Bot 63:3001–3009
Urwin PE, Lilley CJ, Atkinson HJ (2002) Ingestion of double-stranded RNA by preparasitic juvenile cyst nematodes leads to RNA interference. Mol Plant Microbe Interaction 15:747–752
USDA-NASS (2012) Crop production summary. US Department of Agriculture, National Agricultural Statistics Service, Washington, DC 2013. http://www.nass.usda.gov. Accessed May 2014
USDA-NASS (2013) Crop production summary. US Department of Agriculture, National Agricultural Statistics Service, Washington, DC 2013. http://www.nass.usda.gov
Valente MAS, Faria JAQA, Soares-Ramos JRL, Reis PAB, Pinheiro GL, Piovesan ND, Morais AT, Menezes CC, Cano MAO, Fietto LG et al (2009) The ER luminal binding protein (BiP) mediates an increase in drought tolerance in soybean and delays drought-induced leaf senescence in soybean and tobacco. J Exp Bot 60:533–546
Valliyodan B, Nguyen HT (2006) Understanding regulatory networks and engineering for enhanced drought tolerance in plants. Curr Opin Plant Biol 9:189–195
Van Ittersum RR (1997) Concepts in production ecology for analysis and quantification of agricultural input-output combinations. Field Crops Res 52:197–208
Varatto C, Pesaresi P, Meurer J, Oelmuller R, Steiner-Lange S, Salamini F et al (2000) Disruption of the Arabidopsis photosystem I gene psaE1 affects photosynthesis and impairs growth. Plant J 22:115–124
Vendruscolo EC, Schuster I, Pileggi M, Scapim CA, Molinari HB, Marur CJ et al (2007) Stress-induced synthesis of proline confers tolerance to water deficit in transgenic wheat. J Plant Physiol 164:1367–1376
Verkleij FN, Challa H (1988) Diurnal export and carbon economy in an expanding source leaf of cucumber at contrasting source and sink temperature. Physiol Plant 74:284–293
Vogel JT, Walter MH, Giavalisco P, Lytovchenko A, Kohlen W, Charnikhova T et al (2010) SlCCD7 controls strigolactone biosynthesis, shoot branching and mycorrhiza-induced apocarotenoid formation in tomato. Plant J 61:300–311
Voldeng HD, Cober ER, Hume DJ, Gillard C, Morrison MJ (1997) Fifty-eight years of genetic improvement of short-season soybean cultivars in Canada. Crop Sci 37:428–431
von Caemmerer S, Evans JR (2010) Enhancing C3 photosynthesis. Plant Physiol 154:589–592
Waclawovsky AJ, Loureiro ME, Freitas RL, da Silva RC, Cano MAO, Fontes EPB (2006) Evidence for the sucrose-binding protein role in carbohydrate metabolism and transport at early developmental stage. Physiol Plant 128:391–404
Walker DR, All JN, Mcpherson RM, Boerma HR, Parrott WA (2000) Field evaluation of soybean engineered with a synthetic cry1Ac transgene for resistance to corn earworm, soybean looper, velvetbean caterpillar (Lepidoptera: Noctuidae), and lesser cornstalk borer (Lepidoptera: Pyralidae). J Econ Entomol 93:613–622
Walker DR, Narvel JM, Boerma HR, All JN, Parrott WA (2004) A QTL that enhances and broadens Bt insect resistance in soybean. Theor Appl Genet 109:1051–1057
Wang E, Wang J, Zhu X, Hao W, Wang L, Li Q et al (2008) Control of rice grain-filling and yield by a gene with a potential signature of domestication. Nat Genet 40:1370–1374
Wang B, Sang Y, Song J, Gao XQ, Zhang X (2009a) Expression of a rice OsARGOS gene in Arabidopsis promotes cell division and expansion and increases organ size. J Genet Gen 36:31–40
Wang J, Nakazaki T, Chen S, Chen W, Saito H, Tsukiyama T et al (2009b) Identification and characterization of the erect-pose panicle gene EP conferring high grain yield in rice (Oryza sativa L). Theor Appl Genet 119:85–91
Wang Y, Beaith M, Chalifoux M, Ying J, Uchacz T, Sarvas C et al (2009c) Shoot-specific down-regulation of protein farnesyltransferase (alpha-subunit) for yield protection against drought in canola. Mol Plant 2:191–200
Wang GP, Hui Z, Li F, Zhao MR, Zhang J, Wang W (2010) Improvement of heat and drought photosynthetic tolerance in wheat by over-accumulation of glycine betaine. Plant Biotech Rep 4:213–222
Wang X, Liu B, Huang C, Zhang X, Luo C, Cheng X, Yu R, Wu Z (2012) Over expression of Zmda1-1 gene increases seed mass of corn. African J Biotech 11:13387–13395
Wardlaw IF (1990) The control of carbon partitioning in plants. New Phytol 116:341–381
Weber H, Borisjuk L, Wobus U (2005) Molecular physiology of legume seed development. Ann Rev Plant Biol 56:253–279
Wei A, He C, Li B, Li N, Zhang J (2011) The pyramid of transgenes TsVP and BetA effectively enhances the drought tolerance of maize plants. Plant Biotech J 9:216–229
Weichert N, Saalbach I, Weichert H, Kohl S, Erban A, Kopka J et al (2010) Increasing sucrose uptake capacity of wheat grains stimulates storage protein synthesis. Plant Physiol 152:688–710
Westgate ME (2001) Physiology of high yielding corn and soybeans. Iowa State University, Department of Agronomy, Ames, Iowa. brasil.ipni.net/ipniweb/region/brasil.nsf/…/Palestra%20do%20Westgate.pdf. Accessed Dec 2013
Westgate ME, Peterson CM (1993) Flower and pod development in water deficient soybean. J Exp Bot 258:109–117
Wilcox JR, Schapaugh WT Jr, Bernard RL, Cooper RL, Fehr WR, Niehaus MH (1979) Genetic improvement of soybeans in the Midwest. Crop Sci 19:803–805
Wolswinkel P (1985) Phloem unloading and turgor-sensitive transport: factors involved in sink control of assimilate partitioning. Physiol Plant 65:331–339
Wright G (1996) Review of ACIAR selection for water use efficiency in legumes project recommends further research. ACIAR Food Legume Newslett 1996:2–3
Wu X, Shiroto Y, Kishitani S, Ito Y, Toriyama K (2009) Enhanced heat and drought tolerance in transgenic rice seedlings overexpressing OsWRKY11 under the control of HSP101 promoter. Plant Cell Rep 28:21–30
Xiao BZ, Chen X, Xiang CB, Tang N, Zhang QF, Xiong LZ (2009) Evaluation of seven function-known candidate genes for their effects on improving drought resistance of transgenic rice under field conditions. Mol Plant 2:73–83
Xu F, Joshi CP (2010) Overexpression of aspen sucrose synthase gene promotes growth and development of transgenic Arabidopsis plants. Adv BioSci Biotech 1:426–438
Xu C, Jing R, Mao X, Jia X, Chang XA (2007) wheat (Triticum aestivum) protein phosphatase 2 A catalytic subunit gene provides enhanced drought tolerance in tobacco. Ann Bot 99:439–450
Xu M, Li L, Fan Y, Wan J, Wang L (2011) ZmCBF3 overexpression improves tolerance to abiotic stress in transgenic rice (Oryza sativa) without yield penalty. Plant Cell Rep 30(10):1949–1957
Xue W, Xing Y, Weng X, Zhao Y, Tang W, Wang L et al (2008) Natural variation in Ghd7 is an important regulator of heading date and yield potential in rice. Nat Genet 40:761–767
Xue GP, Way HM, Richardson T, Drenth J, Joyce PA, McIntyre CL (2011) Overexpression of TaNAC69 leads to enhanced transcript levels of stress up-regulated genes and dehydration tolerance in bread wheat. Mol Plant 4(4):697–712
Yabuta Y, Motoki T, Yoshimura K, Takada T, Ishikawa T, Shigeoka S (2002) Thylakoid membrane-bound ascorbate peroxidase is a limiting factor of antioxidative systems under photo-oxidative stress. Plant J 32:912–925
Yamada M, Morishita H, Urano K, Shiozaki N, Yamaguchi-Shinozaki K, Shinozaki K et al (2005) Effects of free proline accumulation in petunias under drought stress. J Exp Bot 56:1975–1981
Yanovsky MJ, Kay SA (2002) Molecular basis of seasonal time measurement in Arabidopsis. Nature 419:308–312
Yasuno N, Yasui Y, Takamure I, Kato K (2007) Genetic interaction between 2 tillering genes, Reduced Culm Number 1 (rcn1) and Tillering Dwarf Gene d3, in rice. J Hered 98:169–172
Yin Z, Meng F, Song H, Wang X, Xu X, Yu D (2010) Expression quantitative trait loc analysis of two genes encoding Rubisco activase in soybean. Plant Physiol 152:1625–1637
Yoshida T, Sakuma Y, Todaka D, Maruyama K, Qin F, Mizoi J et al (2008) Functional analysis of an Arabidopsis heat-shock transcription factor HsfA3 in the transcriptional cascade downstream of the DREB2 A stress-regulatory system. Biochem Biophys Res Commun 368:515–521
Zapata F, Danso SKA, Hardarson G, Fried M (1987) Time course of nitrogen fixation in field grown soybean using nitrogen-15 methodology. Agron J 79:172–176
Zeng D, Yan M, Wang Y, Liu X, Qian Q, Li J (2007) Du1, encoding a novel Prp1 protein, regulates starch biosynthesis through affecting the splicing of Wxb pre-mRNAs in rice (Oryza sativa L). Plant Mol Biol 65:501–509
Zhang XL, Zhang ZJ, Chen J, Chen Q, Wang XC, Huang RF (2005) Expressing TERF1 in tobacco enhances drought tolerance and abscisic acid sensitivity during seedling development. Planta 222:494–501
Zhang JY, Broeckling CD, Sumner LW, Wang ZY (2007a) Heterologous expression of two Medicago truncatula putative ERF transcription factor genes, WXP1 and WXP2, in Arabidopsis led to increased leaf wax accumulation and improved drought tolerance, but differential response in freezing tolerance. Plant Mol Biol 64:265–278
Zhang WH, Zhou Y, Dibley KE, Tyerman SD, Furbank RT, Patrick JW (2007b) Nutrient loading of developing seeds. Func Plant Biol 4:314–331
Zhang J, Tan W, Yang XH, Zhang HX (2008) Plastid-expressed choline monooxygenase gene improves salt and drought tolerance through accumulation of glycine betaine in tobacco. Plant Cell Rep 27:1113–1124
Zhang SW, Li CH, Cao J, Zhang YC, Zhang SQ, Xia YF et al (2009) Altered architecture and enhanced drought tolerance in rice via the down-regulation of indole-3-acetic acid by TLD1/OsGH313 activation. Plant Physiol 151:1889–1901
Zhang A, Li F, Li D, Zhang H, Huang R (2010a) Expression of ethylene response factor JERF1 in rice improves tolerance to drought. Planta 232:765–774
Zhang H, Liu W, Wan L, Li F, Dai L, Li D et al (2010b) Functional analyses of ethylene response factor JERF3 with the aim of improving tolerance to drought and osmotic stress in transgenic rice. Trans Res 19:809–818
Zhang L, Tan Q, Lee R, Trethewy A, Lee YH, Tegeder M (2010c) Altered xylem-phloem transfer of amino acids affects metabolism and leads to increased seed yield and oil content in Arabidopsis. Plant Cell 22:3603–3620
Zhang S, Li N, Gao F, Yang A, Zhang J (2010d) Over-expression of TsCBF1 gene confers improved drought tolerance in transgenic maize. Mol Breed 26:455–465
Zhang L, Xiao S, Li W, Feng W, Li J, Wu Z et al (2011a) Overexpression of a Harpin-encoding gene hrf1 in rice enhances drought tolerance. J Exp Bot 62:4229–4238
Zhang X, Zou Z, Gong P, Zhang J, Ziaf K, Li H et al (2011b) Over-expression of microRNA169 confers enhanced drought tolerance to tomato. Biotech Lett 33:403–409
Zhao J, Ren W, Zhi D, Wang L, Xia G (2007) Arabidopsis DREB1 A/CBF3 bestowed transgenic tall fescue increased tolerance to drought stress. Plant Cell Rep 26:1521–1528
Zheng X, Chen B, Lu G, Han B (2009) Overexpression of a NAC transcription factor enhances rice drought and salt tolerance. Biochem Biophys Res Commun 379:985–989
Zhu BC, Su J, Chan MC, Verma DPS, Fan YL, Wu R (1998) Over-expression of a pyrroline-5-carboxylate synthetase gene and analysis of tolerance to water-stress and salt-stress in transgenic rice. Plant Sci 139:41–48
Zhu XG, Portis AR Jr, Long SP (2004) Would transformation of C3 crop plants with foreign Rubisco increase productivity? A computational analysis extrapolating from kinetic properties to canopy photosynthesis. Plant Cell Env 27:155–165
Zhu S, Walker DR, Boerma HR, All JN, Parrott WA (2008) Effects of defoliating insect resistance QTLs and a cry1Ac transgene in soybean near-isogenic lines. Theor Appl Genet 116:455–463
Zhu XG, Long SP, Ort DR (2010) Improving photosynthetic efficiency for greater yield. Ann Rev Plant Biol 61:235–261
Ziska LH, Bunce JA (1995) Growth and photosynthetic response of three soybean cultivars to simultaneous increases in growth temperature and CO2. Physiol Plant 94:575–584
Ziska LH, Bunce JA, Caulfield FA (2001) Rising atmospheric carbon dioxide and seed yield of soybean genotypes. Crop Sci 41:385–391
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2015 Springer Science+Business Media, LLC
About this chapter
Cite this chapter
Ramachandra, D., Madappa, S., Phillips, J., Loida, P., Karunanandaa, B. (2015). Breeding and Biotech Approaches Towards Improving Yield in Soybean. In: Azhakanandam, K., Silverstone, A., Daniell, H., Davey, M. (eds) Recent Advancements in Gene Expression and Enabling Technologies in Crop Plants. Springer, New York, NY. https://doi.org/10.1007/978-1-4939-2202-4_4
Download citation
DOI: https://doi.org/10.1007/978-1-4939-2202-4_4
Published:
Publisher Name: Springer, New York, NY
Print ISBN: 978-1-4939-2201-7
Online ISBN: 978-1-4939-2202-4
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)