Publication:
The role of a bifunctional catalase-peroxidase KatA in protection of Agrobacterium tumefaciens from menadione toxicity

dc.contributor.authorBenjaphorn Prapagdeeen_US
dc.contributor.authorPaiboon Vattanaviboonen_US
dc.contributor.authorSkorn Mongkolsuken_US
dc.contributor.otherChulabhorn Research Instituteen_US
dc.contributor.otherAsian Institute of Technology Thailanden_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-07-24T03:38:10Z
dc.date.available2018-07-24T03:38:10Z
dc.date.issued2004-03-19en_US
dc.description.abstractAgrobacterium tumefaciens is an aerobic plant pathogenic bacterium that is exposed to reactive oxygen species produced either as by-products of aerobic metabolism or by the defense systems of host plants. The physiological function of the bifunctional catalase-peroxidase (KatA) in the protection of A. tumefaciens from reactive oxygen species other than H2O2was evaluated in the katA mutant (PB102). Unexpectedly, PB102 was highly sensitive to the superoxide generator menadione. The expression of katA from a plasmid vector complemented the menadione-hypersensitive phenotype. A. tumefaciens possesses an additional catalase gene, a monofunctional catalase encoded by catE. Neither inactivation nor high-level expression of the catE gene altered the menadione resistance level. Moreover, heterologous expression of the catalase-peroxidase-encoding gene katG from Burkholderia pseudomallei, but not the monofunctional catalase gene katE from Xanthomonas campestris could restore normal levels of menadione resistance to PB102. A recent observation suggests that the menadione resistance phenotype involves increased activities of organic peroxide-metabolizing enzymes. Heterologous expression of X. campestris alkyl hydroperoxide reductase from a plasmid vector failed to complement the menadione-sensitive phenotype of PB102. The level of menadione resistance shows a direct correlation with the level of peroxidase activity of KatA. This is a novel role for KatA and suggests that resistance to menadione toxicity is mediated by a new, and as yet unknown, mechanism in A. tumefaciens. © 2004 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.en_US
dc.identifier.citationFEMS Microbiology Letters. Vol.232, No.2 (2004), 217-223en_US
dc.identifier.doi10.1016/S0378-1097(04)00075-8en_US
dc.identifier.issn03781097en_US
dc.identifier.other2-s2.0-1842471990en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/21213
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=1842471990&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectImmunology and Microbiologyen_US
dc.titleThe role of a bifunctional catalase-peroxidase KatA in protection of Agrobacterium tumefaciens from menadione toxicityen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=1842471990&origin=inwarden_US

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