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Journal articles on the topic 'Tabtoxin'

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Published: 4 June 2021

Last updated: 1 February 2022

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1

Turner, John G., Rihab R. Taha, and Jill Debbage. "Effects of tabtoxin on nitrogen metabolism." Physiologia Plantarum 67, no. 4 (August 1986): 649–53. http://dx.doi.org/10.1111/j.1399-3054.1986.tb05072.x.

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2

Bender, Carol L., Francisco Alarcón-Chaidez, and Dennis C. Gross. "Pseudomonas syringae Phytotoxins: Mode of Action, Regulation, and Biosynthesis by Peptide and Polyketide Synthetases." Microbiology and Molecular Biology Reviews 63, no. 2 (June 1, 1999): 266–92. http://dx.doi.org/10.1128/mmbr.63.2.266-292.1999.

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SUMMARY Coronatine, syringomycin, syringopeptin, tabtoxin, and phaseolotoxin are the most intensively studied phytotoxins of Pseudomonas syringae, and each contributes significantly to bacterial virulence in plants. Coronatine functions partly as a mimic of methyl jasmonate, a hormone synthesized by plants undergoing biological stress. Syringomycin and syringopeptin form pores in plasma membranes, a process that leads to electrolyte leakage. Tabtoxin and phaseolotoxin are strongly antimicrobial and function by inhibiting glutamine synthetase and ornithine carbamoyltransferase, respectively. Genetic analysis has revealed the mechanisms responsible for toxin biosynthesis. Coronatine biosynthesis requires the cooperation of polyketide and peptide synthetases for the assembly of the coronafacic and coronamic acid moieties, respectively. Tabtoxin is derived from the lysine biosynthetic pathway, whereas syringomycin, syringopeptin, and phaseolotoxin biosynthesis requires peptide synthetases. Activation of phytotoxin synthesis is controlled by diverse environmental factors including plant signal molecules and temperature. Genes involved in the regulation of phytotoxin synthesis have been located within the coronatine and syringomycin gene clusters; however, additional regulatory genes are required for the synthesis of these and other phytotoxins. Global regulatory genes such as gacS modulate phytotoxin production in certain pathovars, indicating the complexity of the regulatory circuits controlling phytotoxin synthesis. The coronatine and syringomycin gene clusters have been intensively characterized and show potential for constructing modified polyketides and peptides. Genetic reprogramming of peptide and polyketide synthetases has been successful, and portions of the coronatine and syringomycin gene clusters could be valuable resources in developing new antimicrobial agents.

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3

Liu, Jinyuan, Yi Le, Bin Ye, Yun Zhen, Chunming Zhu, Jian Shen, and Riqing Zhang. "Tabtoxin-Resistant Protein: Overexpression, Purification, and Characterization." Protein Expression and Purification 24, no. 3 (April 2002): 439–44. http://dx.doi.org/10.1006/prep.2001.1586.

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4

Durbin, R. D., and T. F. Uchytil. "The role of zinc in regulating tabtoxin production." Experientia 41, no. 1 (January 1985): 136–37. http://dx.doi.org/10.1007/bf02005915.

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5

He, Hongzhen, Yu Shao, Chen Yuhang, Liu Bingbing, Cao Zhenbo, Jiang Fan, Liu Yiwei, et al. "Preparation of the selenomethionine derivative of tabtoxin resistance protein." Chinese Science Bulletin 46, no. 15 (August 2001): 1304–7. http://dx.doi.org/10.1007/bf03184331.

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6

Lydon, J., and C. D. Patterson. "Detection of tabtoxin-producing strains of Pseudomonas syringae by PCR." Letters in Applied Microbiology 32, no. 3 (March 6, 2001): 166–70. http://dx.doi.org/10.1046/j.1472-765x.2001.00882.x.

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7

Anzai, Hiroyuki, Katsuyoshi Yoneyama, and Isamu Yamaguchi. "The nucleotide sequence of tabtoxin resistance gene (ttr) ofPseudomonas syringaepv.tabaci." Nucleic Acids Research 18, no. 7 (1990): 1890. http://dx.doi.org/10.1093/nar/18.7.1890.

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8

Barta, T. M., T. G. Kinscherf, and D. K. Willis. "Regulation of tabtoxin production by the lemA gene in Pseudomonas syringae." Journal of Bacteriology 174, no. 9 (1992): 3021–29. http://dx.doi.org/10.1128/jb.174.9.3021-3029.1992.

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9

HARZALLAH, D., and L. LAROUS. "THE DECREASE OF TABTOXIN PRODUCED BY Pseudomonas tabaci IN BATCH CULTURE." Biochemical Society Transactions 27, no. 5 (October 1, 1999): A153. http://dx.doi.org/10.1042/bst027a153.

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10

Kinscherf, T. G., R. H. Coleman, T. M. Barta, and D. K. Willis. "Cloning and expression of the tabtoxin biosynthetic region from Pseudomonas syringae." Journal of Bacteriology 173, no. 13 (1991): 4124–32. http://dx.doi.org/10.1128/jb.173.13.4124-4132.1991.

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11

Sun, F., H. He, Y. Ding, M. Bartlam, Y. Le, X. Qin, R. Zhang, et al. "Crystal structure of tabtoxin resistance protein complexed with acetyl coenzyme A." Acta Crystallographica Section A Foundations of Crystallography 58, s1 (August 6, 2002): c113. http://dx.doi.org/10.1107/s0108767302089547.

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12

HARZALLAH, D., and L. LAROUS. "99 The synthesis of tabtoxin peptide bond in Pseudomonas syringae pv. tabaci." Biochemical Society Transactions 26, no. 4 (November 1, 1998): S383. http://dx.doi.org/10.1042/bst026s383.

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13

Kinscherf, Thomas G., and David K. Willis. "The Biosynthetic Gene Cluster for the β-Lactam Antibiotic Tabtoxin in Pseudomonas syringae." Journal of Antibiotics 58, no. 12 (December 2005): 817–21. http://dx.doi.org/10.1038/ja.2005.109.

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14

Ding, Yi, Shentao Li, Xiaofeng Li, Fei Sun, Jinyuan Liu, Nanming Zhao, and Zihe Rao. "Site-Directed Mutagenesis and Preliminary X-Ray Crystallographic Studies of the Tabtoxin Resistance Protein." Protein & Peptide Letters 10, no. 3 (June 1, 2003): 255–63. http://dx.doi.org/10.2174/0929866033478924.

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15

Engst, Karen. "Identification of alysA-Like Gene Required for Tabtoxin Biosynthesis and Pathogenicity inPseudomonas syringaepv.tabaciStrain PTBR2.024." Molecular Plant-Microbe Interactions 5, no. 4 (1992): 322. http://dx.doi.org/10.1094/mpmi-5-322.

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16

Nikolaeva, V., L. Varsano, and M. Eshkenazy. "Wild Fire Resistant Tobacco Plants Obtained from Calluses Cultivated on a Tabtoxin Containing Medium." Biotechnology & Biotechnological Equipment 4, no. 5-6 (January 1990): 62–65. http://dx.doi.org/10.1080/13102818.1990.10818623.

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17

Marek, E. T., and R. C. Dickson. "Cloning and characterization of Saccharomyces cerevisiae genes that confer L-methionine sulfoximine and tabtoxin resistance." Journal of Bacteriology 169, no. 6 (1987): 2440–48. http://dx.doi.org/10.1128/jb.169.6.2440-2448.1987.

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18

Manning, Margot E., Eli J. Danson, and Christopher T. Calderone. "Functional chararacterization of the enzymes TabB and TabD involved in tabtoxin biosynthesis by Pseudomonas syringae." Biochemical and Biophysical Research Communications 496, no. 1 (January 2018): 212–17. http://dx.doi.org/10.1016/j.bbrc.2018.01.028.

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19

Turner, John G. "Activities of ribulose-1,5-bisphosphate carboxylase and glutamine synthetase in isolated mesophyll cells exposed to tabtoxin." Physiological and Molecular Plant Pathology 29, no. 1 (July 1986): 59–68. http://dx.doi.org/10.1016/s0048-4059(86)80038-8.

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20

Barta, T. M., T. G. Kinscherf, T. F. Uchytil, and D. K. Willis. "DNA sequence and transcriptional analysis of the tblA gene required for tabtoxin biosynthesis by Pseudomonas syringae." Applied and Environmental Microbiology 59, no. 2 (1993): 458–66. http://dx.doi.org/10.1128/aem.59.2.458-466.1993.

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21

Turner, John G. "Inhibition of photosynthesis in Nicotiana tabacum leaves treated with tabtoxin and its relation to pigment loss." Physiologia Plantarum 74, no. 3 (November 1988): 549–55. http://dx.doi.org/10.1111/j.1399-3054.1988.tb02017.x.

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22

A. Gallarato, Lucas, Emiliano D. Primo, Ángela T. Lisa, and Mónica N. Garrido. "Choline Promotes Growth and Tabtoxin Production in a <i>Pseudomonas syringae</i> Strain." Advances in Microbiology 02, no. 03 (2012): 327–31. http://dx.doi.org/10.4236/aim.2012.23039.

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23

Levi, C., and R. D. Durbin. "The isolation and properties of a tabtoxin-hydrolysing aminopeptidase from the periplasm of Pseudomonas syringae pv. tabaci." Physiological and Molecular Plant Pathology 28, no. 3 (May 1986): 345–52. http://dx.doi.org/10.1016/s0048-4059(86)80076-5.

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24

He, Hongzhen, Yi Ding, Mark Bartlam, Fei Sun, Yi Le, Xincheng Qin, Hong Tang, et al. "Crystal Structure of Tabtoxin Resistance Protein Complexed with Acetyl Coenzyme A Reveals the Mechanism for β-Lactam Acetylation." Journal of Molecular Biology 325, no. 5 (January 2003): 1019–30. http://dx.doi.org/10.1016/s0022-2836(02)01284-6.

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25

Baldwin, Jack E., Masami Otsuka, and Philip M. Wallace. "Synthetic studies on tabtoxin. Synthesis of a naturally occuring inhibitor of glutamine synthetase, tabtoxinine-β-lactam, and analogues." Tetrahedron 42, no. 12 (January 1986): 3097–110. http://dx.doi.org/10.1016/s0040-4020(01)87377-4.

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26

Arai, T., Y. Arimura, S. Ishikura, and K. Kino. "L-Amino Acid Ligase from Pseudomonas syringae Producing Tabtoxin Can Be Used for Enzymatic Synthesis of Various Functional Peptides." Applied and Environmental Microbiology 79, no. 16 (June 14, 2013): 5023–29. http://dx.doi.org/10.1128/aem.01003-13.

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27

Roth, Patricia, Alfons Hädener, and Christoph Tamm. "Further Studies on the Biosynthesis of Tabtoxin (Wildfire Toxin): Incorporation of [2,3-13C2]Pyruvate into the β-Lactam Moiety." Helvetica Chimica Acta 73, no. 2 (March 14, 1990): 476–82. http://dx.doi.org/10.1002/hlca.19900730228.

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28

Kong, Hye Suk, Daniel P. Roberts, Cheryl D. Patterson, Sarah A. Kuehne, Stephan Heeb, Dilip K. Lakshman, and John Lydon. "Effect of Overexpressing rsmA from Pseudomonas aeruginosa on Virulence of Select Phytotoxin-Producing Strains of P. syringae." Phytopathology® 102, no. 6 (June 2012): 575–87. http://dx.doi.org/10.1094/phyto-09-11-0267.

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The GacS/GacA two-component system functions mechanistically in conjunction with global post-transcriptional regulators of the RsmA family to allow pseudomonads and other bacteria to adapt to changing environmental stimuli. Analysis of this Gac/Rsm signal transduction pathway in phytotoxin-producing pathovars of Pseudmonas syringae is incomplete, particularly with regard to rsmA. Our approach in studying it was to overexpress rsmA in P. syringae strains through introduction of pSK61, a plasmid constitutively expressing this gene. Disease and colonization of plant leaf tissue were consistently diminished in all P. syringae strains tested (pv. phaseolicola NPS3121, pv. syringae B728a, and BR2R) when harboring pSK61 relative to these isolates harboring the empty vector pME6031. Phaseolotoxin, syringomycin, and tabtoxin were not produced in any of these strains when transformed with pSK61. Production of protease and pyoverdin as well as swarming were also diminished in all of these strains when harboring pSK61. In contrast, alginate production, biofilm formation, and the hypersensitive response were diminished in some but not all of these isolates under the same growth conditions. These results indicate that rsmA is consistently important in the overarching phenotypes disease and endophtyic colonization but that its role varies with pathovar in certain underpinning phenotypes in the phytotoxin-producing strains of P. syringae.

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29

He, Hongzhen, Yi Ding, Zhenbo Cao, Yu Shao, Mark Bartlam, Hong Tang, Fan Jiang, et al. "Crystallization and preliminary X-ray crystallographic analysis of native and selenomethionyl recombinant tabtoxin-resistance protein complexed with acetyl-coenzyme A." Acta Crystallographica Section D Biological Crystallography 57, no. 11 (October 25, 2001): 1729–31. http://dx.doi.org/10.1107/s0907444901014202.

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30

Taguchi, Fumiko, Tomoko Suzuki, Yoshishige Inagaki, Kazuhiro Toyoda, Tomonori Shiraishi, and Yuki Ichinose. "The Siderophore Pyoverdine of Pseudomonas syringae pv. tabaci 6605 Is an Intrinsic Virulence Factor in Host Tobacco Infection." Journal of Bacteriology 192, no. 1 (October 23, 2009): 117–26. http://dx.doi.org/10.1128/jb.00689-09.

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ABSTRACT To investigate the role of iron uptake mediated by the siderophore pyoverdine in the virulence of the plant pathogen Pseudomonas syringae pv. tabaci 6605, three predicted pyoverdine synthesis-related genes, pvdJ, pvdL, and fpvA, were mutated. The pvdJ, pvdL, and fpvA genes encode the pyoverdine side chain peptide synthetase III l-Thr-l-Ser component, the pyoverdine chromophore synthetase, and the TonB-dependent ferripyoverdine receptor, respectively. The ΔpvdJ and ΔpvdL mutants were unable to produce pyoverdine in mineral salts-glucose medium, which was used for the iron-depleted condition. Furthermore, the ΔpvdJ and ΔpvdL mutants showed lower abilities to produce tabtoxin, extracellular polysaccharide, and acyl homoserine lactones (AHLs), which are quorum-sensing molecules, and consequently had reduced virulence on host tobacco plants. In contrast, all of the mutants had accelerated swarming ability and increased biosurfactant production, suggesting that swarming motility and biosurfactant production might be negatively controlled by pyoverdine. Scanning electron micrographs of the surfaces of tobacco leaves inoculated with the mutant strains revealed only small amounts of extracellular polymeric matrix around these mutants, indicating disruption of the mature biofilm. Tolerance to antibiotics was drastically increased for the ΔpvdL mutant, as for the ΔpsyI mutant, which is defective in AHL production. These results demonstrated that pyoverdine synthesis and the quorum-sensing system of Pseudomonas syringae pv. tabaci 6605 are indispensable for virulence in host tobacco infection and that AHL may negatively regulate tolerance to antibiotics.

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31

WANI, Shabir Hussain. "Inducing Fungus-Resistance into Plants through Biotechnology." Notulae Scientia Biologicae 2, no. 2 (June 13, 2010): 14–21. http://dx.doi.org/10.15835/nsb224594.

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Plant diseases are caused by a variety of plant pathogens including fungi, and their management requires the use of techniques like transgenic technology, molecular biology, and genetics. There have been attempts to use gene technology as an alternative method to protect plants from microbial diseases, in addition to the development of novel agrochemicals and the conventional breeding of resistant cultivars. Various genes have been introduced into plants, and the enhanced resistance against fungi has been demonstrated. These include: genes that express proteins, peptides, or antimicrobial compounds that are directly toxic to pathogens or that reduce their growth in situ; gene products that directly inhibit pathogen virulence products or enhance plant structural defense genes, that directly or indirectly activate general plant defense responses; and resistance genes involved in the hypersensitive response and in the interactions with virulence factors. The introduction of the tabtoxin acetyltransferase gene, the stilbene synthase gene, the ribosome-inactivation protein gene and the glucose oxidase gene brought enhanced resistance in different plants. Genes encoding hydrolytic enzymes such as chitinase and glucanase, which can deteriorate fungal cell-wall components, are attractive candidates for this approach and are preferentially used for the production of fungal disease-resistant plants. In addition to this, RNA-mediated gene silencing is being tried as a reverse tool for gene targeting in plant diseases caused by fungal pathogens. In this review, different mechanisms of fungal disease resistance through biotechnological approaches are discussed and the recent advances in fungal disease management through transgenic approach are reviewed.

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32

Hwang, Michael S. H., Robyn L. Morgan, Sara F. Sarkar, Pauline W. Wang, and David S. Guttman. "Phylogenetic Characterization of Virulence and Resistance Phenotypes of Pseudomonas syringae." Applied and Environmental Microbiology 71, no. 9 (September 2005): 5182–91. http://dx.doi.org/10.1128/aem.71.9.5182-5191.2005.

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ABSTRACT Individual strains of the plant pathogenic bacterium Pseudomonas syringae vary in their ability to produce toxins, nucleate ice, and resist antimicrobial compounds. These phenotypes enhance virulence, but it is not clear whether they play a dominant role in specific pathogen-host interactions. To investigate the evolution of these virulence-associated phenotypes, we used functional assays to survey for the distribution of these phenotypes among a collection of 95 P. syringae strains. All of these strains were phylogenetically characterized via multilocus sequence typing (MLST). We surveyed for the production of coronatine, phaseolotoxin, syringomycin, and tabtoxin; for resistance to ampicillin, chloramphenicol, rifampin, streptomycin, tetracycline, kanamycin, and copper; and for the ability to nucleate ice at high temperatures via the ice-nucleating protein INA. We found that fewer than 50% of the strains produced toxins and significantly fewer strains than expected produced multiple toxins, leading to the speculation that there is a cost associated with the production of multiple toxins. None of these toxins was associated with host of isolation, and their distribution, relative to core genome phylogeny, indicated extensive horizontal genetic exchange. Most strains were resistant to ampicillin and copper and had the ability to nucleate ice, and yet very few strains were resistant to the other antibiotics. The distribution of the rare resistance phenotypes was also inconsistent with the clonal history of the species and did not associate with host of isolation. The present study provides a robust phylogenetic foundation for the study of these important virulence-associated phenotypes in P. syringae host colonization and pathogenesis.

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33

Müller, Barbara, Alfons Hädener, and Christoph Tamm. "Studies on the Biosynthesis of Tabtoxin (Wildfire Toxin). Origin of the Carbonyl C-Atom of the β-Lactam Moiety from the C1-Pool." Helvetica Chimica Acta 70, no. 2 (March 18, 1987): 412–22. http://dx.doi.org/10.1002/hlca.19870700220.

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34

Koike, S. T., and C. T. Bull. "First Report of Bacterial Leaf Spot of Italian Dandelion (Cichorium intybus) Caused by a Pseudomonas syringae Pathovar in California." Plant Disease 90, no. 2 (February 2006): 245. http://dx.doi.org/10.1094/pd-90-0245a.

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Italian dandelion (Cichorium intybus) is a leafy, nonhead forming chicory plant that is eaten as a fresh vegetable in salads. During the late summer (August through October) of 2002, in the Salinas Valley (Monterey County) in California, a previously unreported disease was found in commercial Italian dandelion fields. Early symptoms were angular, vein delimited, dark, water-soaked leaf spots that measured 2 to 7 mm in diameter. As disease developed, spots retained angular edges but exhibited various irregular shapes. Spots commonly formed along the edges of the leaves; in some cases these spots developed into lesions that measured between 10 and 30 mm long. Spots were visible from adaxial and abaxial sides and were dull black in color. A cream-colored pseudomonad was consistently isolated from leaf spots that were macerated and streaked onto sucrose peptone agar. Fungi were not recovered from any of the spots. Recovered strains were blue-green fluorescent when streaked onto King's medium B agar. Bacterial strains were levan positive, oxidase negative, and arginine dihydrolase negative. Strains did not rot potato slices but induced a hypersensitive reaction on tobacco (Nicotiana tabacum cv. Turk). These data indicated that the bacteria belonged to LOPAT group 1 of Pseudomonas syringae (1). Pathogenicity of six strains was tested by growing inoculum in nutrient broth shake cultures for 48 h, diluting to 106 CFU/ml, and spraying onto 12 6-week-old plants of Italian dandelion cv. Catalogna Special. Untreated control plants were sprayed with sterile nutrient broth. After 10 to 12 days in a greenhouse (24 to 26°C), leaf spots similar to those observed in the field developed on all inoculated plants. Strains were reisolated from the spots and identified as P. syringae. Control plants remained symptomless. These inoculation experiments were done twice and the results were the same. Amplification of repetitive bacterial sequences (repetitive sequence-based polymerase chain reaction [rep-PCR]) demonstrated that all Italian dandelion strains had the same rep-PCR fingerprint, which differed from fingerprints of P. syringae pv. tagetis and P. syringae pv. tabaci. Additionally, toxin specific primers did not amplify tagetitoxin or tabtoxin biosynthesis genes from Italian dandelion strains. To our knowledge, this is the first report of bacterial leaf spot of commercially grown Italian dandelion in California caused by a P. syringae pathovar. Because fields were irrigated with overhead sprinklers, the disease was severe in several fields and as much as 30% of those plantings were not harvested. Reference: (1) R. A. Lelliott et al. J. Appl. Bacteriol. 29:470, 1966.

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35

BALDWIN, J. E., P. D. BAILEY, G. GALLACHER, M. OTSUKA, K. A. SINGLETON, P. M. WALLACE, K. PROUT, and W. M. WOLF. "ChemInform Abstract: STEREOSPECIFIC SYNTHESIS OF TABTOXIN." Chemischer Informationsdienst 16, no. 16 (April 23, 1985). http://dx.doi.org/10.1002/chin.198516346.

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36

BALDWIN, J. E., M. OTSUKA, and P. M. WALLACE. "ChemInform Abstract: Synthetic Studies on Tabtoxin. Synthesis of a Naturally Occurring Inhibitor of Glutamine Synthetase, Tabtoxinine-β-lactam, and Analogues." Chemischer Informationsdienst 17, no. 43 (October 28, 1986). http://dx.doi.org/10.1002/chin.198643293.

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