Production and Characterization of an Antifungal Compound from Pseudomonas protegens Strain W45

被引:5
作者
Bajpai A. [1 ]
Singh B. [2 ]
Joshi S. [3 ]
Johri B.N. [1 ]
机构
[1] Department of Biotechnology, Barkatullah University, Bhopal, 462026, M.P.
[2] Department of Microbiology, Maharshi Dayanand University, Rohtak, Haryana
[3] Department of Microbiology, University of Delhi South Campus, New Delhi
关键词
Antifungal compound; Optimization; Pseudomonas protegens; Rhizobacteria; Sclerotinia sclerotiorum;
D O I
10.1007/s40011-017-0844-1
中图分类号
学科分类号
摘要
Pseudomonas protegens strain W45 recovered from rhizosphere of wheat possesses potential to produce an antifungal compound in the culture medium. Therefore, to enhance its production, statistical optimization of medium was employed. Peptone, glycerol and incubation period were identified as significant variables affecting its production. These variables were further optimized by response surface methodology that resulted in 38% enhancement in inhibition zone with optimal values of 2.5%, 1.49% and 48 h for peptone, glycerol and incubation period, respectively. PCR amplification by gene specific primers for phloroglucinol, pyrrolnitrin and pyoluteorin resulted in amplicon of 745, 719 and 773 bp respectively, confirming the presence of all three genes. Antifungal compound was purified by thin layer chromatography. Gas chromatography mass spectrometry analysis of the methanolic extract reveals the presence of pyrrole type antifungal molecule 3-(2-methylpropyl)-hexahydropyrrolo [1,2-a]pyrazine-1,4-dione (C11H18N2O2). The compound significantly inhibited the growth of Sclerotinia sclerotiorum. © 2017, The National Academy of Sciences, India.
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页码:1081 / 1089
页数:8
相关论文
共 44 条
[11]  
Yang F., Long L., Sun X., Wu H., Li T., Et al., Optimization of medium using response surface methodology for lipid production by Scenedesmus sp, Mar Drugs, 12, pp. 1245-1257, (2014)
[12]  
Mavrodi O.V., Spadden M., Gardener B.B., Mavrodi D.V., Bonsall R.F., Et al., Genetic diversity of phlD from 2,4-diacetylphloroglucinol- producing fluorescent Pseudomonas spp, Phytopathology, 91, pp. 35-43, (2001)
[13]  
McSpadden Gardener B.B., Mavrodi D.V., Thomashow L.S., Weller D.M., A rapid polymerase chain reaction-based assay characterizing rhizosphere populations of 2,4-diacetylphloroglucinol producing bacteria, Phytopathology, 91, pp. 44-54, (2001)
[14]  
de Souza J.T., Raaijmakers J.M., Polymorphisms within the prnD and pltC genes from pyrrolnitrin and pyoluteorin producing Pseudomonas and Burkholderia spp, FEMS Microbiol Ecol, 43, pp. 21-34, (2003)
[15]  
Mazzola M., Cook R.J., Thomashow L.S., Weller D.M., Pierson L.S., Contribution of phenazine antibiotic biosynthesis to the ecological competence of Fluorescent Pseudomonas in soil habitats, Appl Environ Microbiol, 8, pp. 2616-2624, (1992)
[16]  
Kumar A., Saini S., Wray V., Nimtz M., Prakash A., Et al., Characterization of an antifungal compound produced by Bacillus sp. strain A(5)F that inhibits Sclerotinia sclerotiorum, J Basic Microbiol, 52, pp. 670-678, (2012)
[17]  
Park J.Y., Oh S.A., Anderson A.J., Neiswender J., Kim J.C., Production of the antifungal compound phenazine and pyrrolnitrin from Pseudomonas chlororaphis 06 is differentially regulated by glucose, Lett Appl Microbiol, 52, pp. 532-537, (2011)
[18]  
Zhou T., Chen D., Li C., Sun Q., Li L., Et al., Isolation and characterization of Pseudomonas brassicacearum J12 as an antagonist against Ralstonia solanacearum and identification of its antimicrobial components, Microbiol Res, 167, pp. 388-394, (2012)
[19]  
Dharni S., Alam M., Kalani K., Khaliq A., Samad A., Et al., Production, purification, and characterization of antifungal metabolite from Pseudomonas aeruginosa SD12, a new strain obtained from tannery waste polluted soil, J Microbiol Biotechnol, 22, pp. 674-683, (2012)
[20]  
Perez C., Paul M., Bezique P., An antifungal assay by the agar well diffusion method, Acta Biomed Group Exper, 15, pp. 113-115, (1990)