Abstract
Bacillusamyloliquefaciens C06, a potential agent in biological preservation of post-harvest fruit, was found to secrete extra-cellular γ-polyglutamic acid (γ-PGA) in liquid culture. In this work, M306, a transposon mutant of B. amyloliquefaciens C06, defective in forming structured colony and displaying enhanced ability of producing γ-PGA, was obtained. Inverse PCR and quantitative reverse transcription PCR (qRT-PCR) analysis demonstrated that the defective phenotype in M306 was associated with an ORF showing high similarity to RBAM_034550 from B. amyloliquefaciens FZB42. In this paper, the ORF was designated pbrA, standing for γ-PGA production and biofilm formation regulatory factor. qRT-PCR analysis also indicated that pbrA down-regulated mRNA expression of epsD and yqxM, the crucial genes involved in biofilm formation, but affected little on expression of ywtB, the gene directing γ-PGA synthesis. Evaluations in γ-PGA productivity of wild-type C06 and its mutants C06ΔepsA and C06ΔtasA, respectively, deficient in producing exopolysaccharides (EPS) and TasA, revealed that γ-PGA overproduction in M306 was probably due to the redistributed metabolic flux caused by defective production of EPS.
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Acknowledgements
This research is funded by Agriculture and Agri-food Canada and also supported by grants from National Natural Science Fund of China (30570041), the National 863 Program of China (2006AA10Z172), the Program of International Science and Technology Cooperation (2009DFA32740), and the Special Nonprofit Scientific Research Program, P. R. China (3–23). J. Liu received a graduate scholarship from the China Scholarship Council.
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Liu, J., Ma, X., Wang, Y. et al. Depressed Biofilm Production in Bacillus amyloliquefaciens C06 Causes γ-Polyglutamic Acid (γ-PGA) Overproduction. Curr Microbiol 62, 235–241 (2011). https://doi.org/10.1007/s00284-010-9696-0
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DOI: https://doi.org/10.1007/s00284-010-9696-0