Co-production of two new peptide antibiotics by a bacterial isolate Paenibacillus alvei NP75

被引:16
作者
Anandaraj, Balaiah [1 ]
Vellaichamy, Adaikkalam [2 ]
Kachman, Maureen [2 ]
Selvamanikandan, Athinarayanan [1 ]
Pegu, Shyamanta [1 ]
Murugan, Vadivel [1 ]
机构
[1] Anna Univ, Genet Engn Unit, Ctr Biotechnol, Madras 600025, Tamil Nadu, India
[2] Univ Michigan, Ann Arbor, MI 48109 USA
关键词
Paenibacillus alvei; Peptide antibiotics; Co-production; Antagonistic activity; Protease; Mass-spectrometry analysis; IDENTIFICATION; BIOSYNTHESIS; PURIFICATION; STRAIN;
D O I
10.1016/j.bbrc.2008.12.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Two new peptide antibiotics were secreted by a Gram-positive bacterial strain isolated from fermented tomato fruit. Based on its 99% 16S rDNA sequence similarity with Paenibacillus alvei, the isolate was designated as P alvei NP75. Among these two peptides, one is active against Gram-positive pathogens while the other against Gram-negative pathogens; thus these peptides were named as paenibacillin P and paenibacillin N, respectively. After the Purification of those peptide antibiotics from the cell free culture Supernatant by RP-HPLC, they were analyzed for their temperature sensitivity and susceptibility to proteases. Higher-temperature tolerant paenibacillin N was easily degraded by proteinase K, while the temperature sensitive paenibacillin P was not affected by any of the proteases used in this study other than a specific protease that was secreted by the same NP75 strain. Mass-spectrometry analysis of the above peptide antibiotics further confirmed their distinction among the known peptide antibiotics. We are reporting first of its kind the co-production of two different new peptide antibiotics from a single bacterial isolate of P. alvei strain. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:179 / 185
页数:7
相关论文
共 26 条
[1]   Strategies to evade false positives in the in situ analysis of peptide antibiotics in SDS-PAGE gels [J].
Anandaraj, Balaiah ;
Selvamanikandan, Athinarayanan ;
Mittal, Prabakar ;
Elavarasi, Natarajan ;
Thangadurai, Chinnathambi ;
Murugan, Vadivel .
ANALYTICAL BIOCHEMISTRY, 2008, 373 (02) :401-403
[2]   Recently approved and investigational antibiotics for treatment of severe infections caused by Gram-positive bacteria [J].
Appelbaum, PC ;
Jacobs, MR .
CURRENT OPINION IN MICROBIOLOGY, 2005, 8 (05) :510-517
[3]   MODE OF ACTION OF PEDIOCIN ACH FROM PEDIOCOCCUS-ACIDILACTICI-H ON SENSITIVE BACTERIAL STRAINS [J].
BHUNIA, AK ;
JOHNSON, MC ;
RAY, B ;
KALCHAYANAND, N .
JOURNAL OF APPLIED BACTERIOLOGY, 1991, 70 (01) :25-33
[4]   Purification and partial chemical characterization of the antimicrobial peptide cerein 8A [J].
Bizani, D ;
Dominguez, APM ;
Brandelli, A .
LETTERS IN APPLIED MICROBIOLOGY, 2005, 41 (03) :269-273
[5]   Identification and functional analysis of the fusaricidin biosynthetic gene of Paenibacillus polymyxa E681 [J].
Choi, Soo-Keun ;
Park, Soo-Young ;
Kim, Rumi ;
Lee, Choong-Hwan ;
Kim, Jihyun F. ;
Park, Seung-Hwan .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2008, 365 (01) :89-95
[6]  
DELVESBROUGHTON J, 1990, FOOD TECHNOL-CHICAGO, V44, P100
[7]   Ribosomally synthesized antibacterial peptides in gram positive bacteria [J].
Diep, DB ;
Nes, IF .
CURRENT DRUG TARGETS, 2002, 3 (02) :107-122
[8]  
Dittmann E, 2001, APPL MICROBIOL BIOT, V57, P467
[9]   Biosynthesis of nonribosomal peptides [J].
Finking, R ;
Marahiel, MA .
ANNUAL REVIEW OF MICROBIOLOGY, 2004, 58 :453-488
[10]   FACILITATING QUALITY-CONTROL OF THE ANTI-MICROBIAL SUSCEPTIBILITY TEST [J].
FLOURNOY, DJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 1981, 13 (01) :231-232