Abstract
Agrobacterium tumefaciens is a gram-negative soil bacterium that causes crown gall tumors on a broad spectrum of dicotyledonous plants (for reviews see: BINNS and THOMASHOW 1988; WINANS 1992; ZAMBRYSKI 1992) . This pathogenic response results from the activities of a large tumor-inducing (Ti) plasmid that resides in many but not all agrobacteria found in the rhizosphere. The infection and transformation process is a complex series of interactions between host and pathogen that ultimately leads to the transfer of DNA (the T-DNA) from the Ti plasmid into the plant cell where it is integrated into the nuclear genome. Expression of this T-DNA results in the production of two classes of protein products: (1) enzymes that synthesize plant hormones capable of stimulating continuous cell division in the transformed cells and (2) enzymes that synthesize unique amino acid:sugar acid conjugates, termed opines, that are not metabolizable by the host cell but are metabolized by the inciting bacterium, providing it with a dedicated nitrogen and carbon source.
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Agron PG, Ditta GS, Helinski DR (1993) Oxygen regulation of nifA transcription in vitro. Proc Natl Acad Sci USA 90: 3506–3510
Ankenbauer RG, Best EA, Palanca CA, Nester EW (1991) Mutants of the Agrobacterium tumefaciens virA gene exhibiting acetosyringone-independent expression of the vir regulon. Mol Plant Microbe Interact 4: 400–406
Aoyama T, Takanami M, Makino K, Oka A (1991) Cross-talk between the virulence and phosphate regulons of Agrobacterium tumefaciens caused by an unusual interaction of the transcriptional activator with a regulatory DNA element. Mol Gen Genet 227: 385–390
Arico B, Miller J, Roy C, Stibitz S, Monack D, Falkow S, Gross R, Rappuoli R (1989) Sequences required for expression of Bordetella pertussis virulence factors share homology with prokaryotic signal transduction proteins. Proc Natl Acad Sci USA 86: 6671–6675
Ashby AM, Watson MD, Loake GJ, Shaw CH (1988) Ti plasmid-specified chemotaxis of Agrobacterium tumefaciens C58C1 toward vir-inducing phenolic compounds and soluble factors from monocotyledonous and dicotyledonous plants. J Bacteriol 170: 4181–4187
Banta LM, Joerger RD, Howitz VR, Campbell AM, Binns AN (1994) Glu-255 outside the predicted ChvE binding site in VirA is crucial for sugar enhancement of acetosyringene perception by Agrobacterium tumefaciens. J Bacteriol 176: 3242–3249
Binns AN (1991) Transformation of wall deficient culture tobacco protoplasts by Agrobacterium tumefaciens. Plant Physiol 96: 498–506
Binns AN, Thomashow MF (1988) Cell biology of Agrobacterium infection and transformation of plants. Annu Rev Microbiol 42: 575–606
Binns AN, Joerger RD, Banta LM, Lee K, Lynn DG (1993). Molecular and chemical analysis of signal perception by Agrobacterium. In: Nester EW, Verma DPS (eds) Advances in molecular genetics of plant-microbe interactions. Kluwer Academic, Dordrecht, pp 51–61
Braun AC (1947) Thermal studies on tumor inception in the crown gall disease. Am J Bot 30: 674–677
Braun AC (1952) Conditioning of the host cells is a factor in the transformation process in crown gall. Growth 16: 65–74
Braun AC, Mandle RJ (1948) Studies on the inactivation of the tumor inducing principle in crown gall. Growth 12: 255–269
Braun AC, Stonier T (1958) Morphology and physiology of plant tumors. Protoplasmatologia 10 (5a): 1–93
Cangelosi GA, Hung L, Puvanesarajah V, Stacey G, Ozga AD, Leigh JA, Nester EW (1987) Common loci for Agrobacterium tumefaciens and Rhizobium meliloti exopolysaccharide synthesis and their role in plant interactions. J Bacteriol 169: 2086–2091
Cangelosi GA, Martinetti G, Leigh JA, Lee CC, Theines C, Nester EW (1989) Role of Agrobacterium tumefaciens ChvA protein in export of b-1,2-glucan. J Bacteriol 171: 1609–1615
Cangelosi GA, Ankenbauer RG, Nester EW (1990a) Sugars induce the Agrobacterium virulence genes through a periplasmic binding protein and a transmembrane signal protein. Proc Natl Acad Sci USA 87: 6708–6712
Cangelosi GA, Martinetti G, Nester EW (1990b) Osmosensitivity phenotypes of Agrobacterium tumefaciens mutants that lack periplasmic ß-1,2-glucan. J Bacteriol 172: 2172–2174
Chang C-H, Winans SC (1992) Functional roles assigned to the periplasmic, linker, and receiver domains of the Agrobacterium tumefaciens VirA protein. J Bacteriol 174: 7033–7039
Charles TC, Nester EW (1993) A chromosomally encoded two-component sensory transduction system is required for virulence of Agrobacterium tumefaciens. J Bacteriol 175: 6614–6625
Close TJ, Tait RC, Kado CI (1985) Regulation of Ti plasmid virulence genes by a chromosomal locus of Agrobacterium tumefaciens. J Bacteriol 164: 774–781
Close TJ, Rogowsky PM, Kado CI, Winans SC, Yanofsky MF, Nester EW (1987) Dual control of Agrobacterium tumefaciens Ti plasmid virulence genes. J Bacteriol 169: 5113–5117
Cooley MB, D’Sousa MR, Kado CI (1991) virC and virD operons of the Agrobacterium Ti plasmid are regulated by the ros chromosomal gene: analysis of the cloned ros gene. J Bacteriol 173: 2608–2616
Das A, Stachel P, Ebert P, Allenza A, Montoya A, Nester EW (1986) Promoters of Agro-bacterium tumefaciens Ti-plasmid virulence genes. Nucleic Acids Res 14: 1355–1364
Douglas CJ, Halperin W, Nester EW (1982) Agrobacterium tumefaciens mutants affected in attachment to plant cells. J Bacteriol 152: 1265–1275
Douglas CJ, Staneloni RJ, Rubin RA, Nester EW (1985) Identification and genetic analysis of an Agrobacterium tumefaciens chromosomal virulence region. J Bacteriol 161: 850–860
Duban ME, Lee K, Lynn DG (1993) Agrobacterium tumefaciens: mechanisitic specificity in a generic signaling strategy. Mol Microbiol 7: 637–645
Endoh H, Oka A (1993) Functional analysis of the VirG-like domain contained in the Agrobacterium VirA protein that senses plant factors. Plant Cell Physiol 34: 227–235
Fry, SC (1983) Feruloylated pectins from the primary cell wall: their structure and possible functions. Planta 157: 111–123
Gurlitz RHG, Lamb PW, Matthysse AG (1987) Involvement of carrot surface proteins in attachment of Agrobacterium tumefaciens. Plant Physiol 83: 564–568
Han DC, Chen C-Y, Winans SC (1992) Altered-function mutations of the transcriptional regulatory gene virG of Agrobacterium tumefaciens. J Bacteriol 174: 7040–7043
Hartman FC (1971) Haloacetol phosphates. Characterization of the active site of rabbit muscle triose phosphate isomerase. Biochemistry 10: 146–154
Hawes MC, Smith LY (1989) Requirement for Chemotaxis in pathogenicity of Agrobacterium tumefaciens on roots of soil-grown pea plants. J Bacteriol 171: 5668–5671
Hess KM, Dudley MW, Lynn DG, Joerger RD, Binns AN (1991) Mechanism of phenolic activation of Agrobacterium virulence genes: development of a specific inhibitor of bacterial sensor/response systems. Proc Natl Acad Sci USA 88: 7854–7858
Hooykaas PJJ, Klapwijk PM, Nuti MP, Schilperoort RA, Rorsch A (1977) Transfer of the Agrobacterium tumefaciens Ti plasmid to avirulent agrobacteria and to Rhizobium ex planta. J Gen Microbiol 98: 477–484
Hrabak E, Willis DK (1992) The lemA gene required for pathogenicity of Pseudomonas syringae pv. syringae on bean is a member of a family of two-component regulators. J Bacteriol 174: 3011–3020
Huang M-LAW, Cangelosi GA, Halperin W, Nester EW (1990a) A chromosomal Agrobacterium tumefaciens gene required for effective plant signal transduction. J Bacteriol 172: 1814–1822
Huang Y, Morel P, Powell B, Kado C (1990b) VirA, a coregulator of Ti-specified virulence genes, is phosphorylated in vitro. J Bacteriol 172: 1142–1144
Jin S, Prusti RK, Roitsch T, Ankenbauer RG, Nester EW (1990a) Phosphorylation of the virG protein of Agrobacterium tumefaciens by the autophosphorylated virA protein: essential role in biological activity of virG. J Bacteriol 172: 4945–4950
Jin S, Roitsch T, Ankenbauer RG, Gordon MP, Nester EW (1990b) The VirA protein of Agrobacterium tumefaciens is autophosphorylated and is essential for vir gene regulation. J Bacteriol 172: 525–530
Jin S, Roitsch T, Christie PJ, Nester EW (1990c) The regulatory virG protein specifically binds to a cisacting regulatory sequence involved in transcriptional activation of Agrobacterium tumefaciens virulence genes. J Bacteriol 172: 531–537
Jin S, Song Y-n, Pan SQ, Nester EW (1993) Characterization of a virG mutation that confers virulence gene expression in Agrobacterium. Mol Microbiol 7: 555–562
Kahl G (1982) Molecular biology of wound healing: the conditioning phenomenon. In: Schell J, Kahl G (ed) Molecular biology of plant tumors. Academic, New York, pp 211–267
Kudirka DT, Colburn SM, Hinchee MA, Wright MS (1986) Interactions of Agrobacterium tumefaciens with soybean (Glycine ma (L.) Merr.) leaf expiants in tissue culture. Can J Bot 28: 808–817
Lamb CJ, Lawton MA, Dron M, Dixon RA (1989) Signals and transduction mechanisms for activation of plant defenses against microbial attack. Cell 56: 215–224
Lee K, Dudley MW, Hess KM, Lynn DG, Joerger RD, Binns AN (1992) Mechanisms of activation of Agrobacterium virulence genes: identification of phenol-binding proteins. Proc Natl Acad Sci USA 89: 8666–8670
Lee TS, Purse JG, Pryce RJ, Horgan R, Wareing PF (1981) Dihydroconiferyl alcohol - a cell division factor from Acer species. Planta 152: 571–577
Leroux B, Yanofsky MF, Winans SC, Ward JE, Ziegler SF, Nester EW (1987) Characterization of the virA locus of Agrobacterium tumefaciens: a transcriptional regulator and host range determinant. EMBO J 6: 849–856
Lewis NG, Yamamoto E (1990) Lignin: Occurrence, biogenesis and biodégradation. Annu Rev Plant Physiol Plant Mol Biol 41: 455–496
Lipetz J (1966) Crown gall tumorigenesis. II. Relations between wound healing and the tumorigenic response. Cancer Res 26: 1597–1605
Loake GJ, Ashby AM, Shaw CH (1988) Attraction of Agrobacterium tumefaciens C58C1 towards sugars involves a highly sensitive chemotaxis system. J Gen Microbiol 134: 1427–1432
Lois AF, Ditta GS, Helinski DR (1993a) The oxygen sensor FixL of Rhizobium meliloti is a membrane protein containing four possible transmembrane segments. J Bacteriol 175: 1103–1109
Lois AF, Weinstein M, Ditta GS, Helinski DR (1993b) Autophosphorylation and phosphatase activities of the oxygen-sensing protein FixL of Rhizobium meliloti are coordinated regulated by oxygen. J Biol Chem 268: 4370–4375
Machida Y, Shimoda N, Yamamoto-Toyoda A, Takahashi Y, Nishihama R, Aoki S, Matsouka K, Nakamura K, Yoshioka Y, Ohba T, Obata RT (1993) Molecular interactions between Agrobacterium and plant cells. In: Nester EW, Verma DPS (eds) Advances in molecular genetics of plant-microbe interactions. Kluwer Academic, Dordrecht, pp 85–96
Mantis NJ, Winans SC (1992) The Agrobacterium tumefaciens vir gene transcriptional activator virG is transcriptionally induced by acidic pH and other stress stimuli. J Bacteriol 174: 1189–1196
Mantis NJ, Winans SC (1993) The chromosomal response regulatory gene chvl of Agrobacterium tumefaciens complements an Escherichia coli phoB mutation and is required for virulence. J Bacteriol 175: 6626–6636
Matthyssee, AG (1987) Characterization of nonattaching mutants of Agrobacterium tumefaciens. J Bacteriol 169: 313–323
McCleary W, Zusman DR (1990) FrzE of Myxococcus xanthus is homologous to both CheA and CheY of Salmonella typhimurium. Proc Natl Acad Sci USA 87: 5898–5902
Melchers LS, Regensburg-Tuïnk AJG, Schilperoort RA, Hooykaas PJJ (1989a) Specificity of signal molecules in the activation of Agrobacterium virulence expression. Mol Microbiol 3: 969–977
Melchers LS, Regensburg-Tuïnk TJG, Bourret RB, Sedee NJA, Schilperoort RA, Hooykaas PJJ (1989b) Membrane topology and functional analysis of the sensory protein virA of Agrobacterium tumefaciens. EMBO J 8: 1919–1925
Neff NT, Binns AN (1985) Agrobacterium tumefaciens interaction with suspension-cultured tomato cells. Plant Physiol 77: 35–42
Neff NT, Binns AN, Brandt C (1987) Inhibitory effects of a pectin-enriched tomato cell wall fraction on Agrobacterium tumefaciens binding and tumor formation. Plant Physiol 83: 525–528
Palmer ACV, Shaw CH (1992) The role of VirA and VirG phosphorylation in chemotaxis towards acetosyringone by Agrobacterium tumefaciens. J Gen Microbiol 138: 2509–2514
Parke D, Ornston NL, Nester EW (1987) Chemotaxis to plant phenolic inducers of virulence genes is constitutively expressed in the absence of the Ti plasmid in Agrobacterium tumefaciens. J Bacteriol 169: 5336–5338
Parkinson JS (1993) Signal transduction schemes of bacteria. Cell 73: 857–871
Pazour GJ, Das A (1990) virG, an Agrobacterium tumefaciens transcriptional activator, initiates translation at a UUG codon and is a sequence-specific DNA-binding protein. J Bacteriol 172: 1241–1249
Pazour GJ, Ta, CN, Das A (1991) Mutants of Agrobacterium tumefaciens with elevated vir gene expression. Proc Natl Acad Sci USA 88: 6941–6945
Pazour GJ, Ta, CN, Das A (1992) Constitutive mutations of Agrobacterium tumefaciens transcriptional activator of virG. J Bacteriol 174: 4169–4174
Powell BS, Rogowsky PM, Kado CI (1989) virG of Agrobacterium tumefaciens Ti plasmid pTiC58 encodes a DNA binding protein. Mol Microbiol 3: 411–4119
Shaw CH, Ashby AM, Brown A, Royal C, Loake GJ, Shaw CH (1988) virA and virG are the Ti-plasmid functions required for Chemotaxis of Agrobacterium tumefaciens towards acetosyringone. Mol Microbiol 2: 413–417
Shimoda T, Toyoda-Yamamoto A, Nagamine J, Usami S, Katayama M, Sakagami Y, Machida Y (1990) Control of expression of Agrobacterium vir genes by synergistic actions of phenolic signal molecules and monosaccharides. Proc Natl Acad Sci USA 87: 6684–6688
Spencer PA, Towers GHN (1988) Specificity of signal compounds detected by Agrobacterium tumefaciens. Phytochemistry 27: 2781–2785
Stachel SE, Zambryski PC (1986) VirA and virG control the plant-induced activation of the T-DNA transfer process of A. tumefaciens. Cell 46: 325–333
Stachel SE, An G, Flores C, Nester EW (1985a) A Tn3 IcZ transposon for the random generation of ß-galactosidase gene fusions: application to the analysis of gene expression in Agrobacterium. EMBO J 4: 891–898
Stachel SE, Messens E, Van Montagu M, Zambryski P (1985b) Identification of the signal molecules produced by wounded plant cells that activate T-DNA transfer in Agrobacterium tumefaciens. Nature 318: 624–629
Stachel SE, Nester EW, Zambryski PC (1986) A plant cell factor induces Agrobacterium tumefaciens vir gene expression. Proc Natl Acad Sci USA 83: 379–383
Stout V, Gottesman S (1990) RcsB and RcsC: a two-component regulator of capsule synthesis in Escherichia coli. J Bacteriol 172: 659–669
Stock JB, Stock AM, Mottonen JM (1990) Signal transduction in bacteria. Nature 344: 395–400
Tan K-S, Hoson T, Masuda Y, Kamisaka S (1992) Involvement of cell wall-bound diferulic acid in lightinduced decrease in growth rate and cell wall extensibility of Oryza coleoptiles. Plant Cell Physiol 33: 103–108
Teutonico RA, Dudley MW, Orr JD, Lynn DG, Binns AN (1991) Activity and accumulation of cell divisionpromoting phenolics in tobacco tissue cultures. Plant Physiol 97: 288–297
Thomashow MF, Karlinsey JE, Marks JR, Hurlbert RE (1987) Identification of a new virulence locus in Agrobacterium tumefaciens that affects polysaccharide composition and plant cell attachment. J Bacteriol 169: 3209–3216
Turk SCHJ, P., VLR, Sonneveld E, Hooykaas PJJ (1993b) The chimeric VirA-Tar receptor protein is locked into a highly responsive state. J Bacteriol 175: 5706–5709
Turk SCH, Nester EW, Hooykaas PJJ (1993a) The virA promoter is a host-range determinant in Agrobacterium tumefaciens. Mol Microbiol 7: 719–724
Turk SCHJ, P., VLR, Sonneveld E, Hooykaas PJJ (1993b) The chimeric VirA-Tar receptor protein is locked into a highly responsive state. J Bacteriol 175: 5706–5709
Uttaro AD, Cangelosi GA, Geremia RA, Nester EW, Ugalde RA (1990) Biochemical characterization of avirulent exoC mutants of Agrobacterium tumefaciens. J Bacteriol 172: 1640–1646
van Veen R (1988) Strategies of bacteria in their interaction with plants; analogies and specialization. PhD dissertation, Rijksuniversiteit Leiden
Veluthambi K, Krishman M, Gould JH, Smith RH, Gelvin SB (1989) Opines stimulate induction of the vir genes of Agrobacterium tumefaciens Ti plasmid. J Bacteriol 171: 3696–3703
Wagner VT, Matthysse AG (1992) Involvement of a vitronectin-like protein in attachment of Agrobacterium tumefaciens to carrot suspension culture cells. J Bacteriol 174: 5999–6003
Wanner BL (1993) Gene regulation by phosphate in enteric bacteria. J Cell Biochem 51: 47–54
Winans SC (1990) Transcriptional induction of an Agrobacterium regulatory gene at tandem promoters by plant-released phenolic compounds, phosphate starvation, and acidic growth media. J Bacteriol 172: 2433–2438
Winans SC (1992) Two-way chemical signaling in Agrobacterium -plant interactions. Microbiol Rev 56: 12–31
Winans SC, Kerstetter RA, Nester EW (1988) Transcriptional regulation of the virA and virG genes of Agrobacterium tumefaciens. J Bacteriol 170: 4047–4054
Winans SC, Kerstetter RA, Ward JE, Nester EW (1989) A protein required for transcriptional regulation of Agrobacterium virulence genes spans the cytoplasmic membrane. J Bacteriol 171: 1616–1622
Yanofsky M, Lowe B, Montoya A, Rubin R, Krul W, Gordon M, Nester EW (1985) Molecular and genetic analysis of factors controlling host range in Agrobacterium tumefaciens. Mol Gen Genet 201: 237–246
Zambryski PC (1992) Chronicles from the Agrobacterium-plant cell DNA transfer story. Annu Rev Plant Physiol Plant Mol Biol 43: 465–490
Zorreguieta A, Geremia RA, Cavaignac S, Cangelosi GA, Nester EW, Ugalde RA (1988) Identification of the product of an Agrobacterium tumefaciens chromosomal virulence gene. Mol Plant Microbe Interact 1: 121–127
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Binns, A.N., Howitz, V.R. (1994). The Genetic and Chemical Basis of Recognition in the Agrobacterium: Plant Interaction. In: Dangl, J.L. (eds) Bacterial Pathogenesis of Plants and Animals. Current Topics in Microbiology and Immunology, vol 192. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-78624-2_6
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