Characterization, N-terminal sequencing and classification of cerein MRX1, a novel bacteriocin purified from a newly isolated bacterium:: Bacillus cereus MRX1

被引:29
作者
Sebei, S.
Zendo, T.
Boudabous, A.
Nakayama, J.
Sonomoto, K.
机构
[1] Kyushu Univ, Grad Sch, Fac Agr,Div Microbial Sci & Technol,Lab Microbial, Dept Biosci & Biotechnol,Higashi Ku, Fukuoka 8128581, Japan
[2] Fac Sci Tunis, Dept Biol, Microbiol Lab, Tunis 1060, Tunisia
关键词
antimicrobial peptide; Bacillus cereus; bacteriocin; purification; sequencing;
D O I
10.1111/j.1365-2672.2007.03395.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aim: To purify and characterize the bacteriocin produced by strain MRX1. Methods and Results: A bacteriocin-producing strain was isolated and identified as Bacillus cereus. The bacteriocin, called cerein MRX1, was purified from the culture supernatant using hydrophobic interaction, cation-exchange chromatography and RP-HPLC. It could also be purified in abundance from the cell surfaces of the producer strain. Mass spectrometry revealed its molecular mass of 3137.93 Da. Sequencing of chemically modified bacteriocin identified its partial sequence: DWTCWSCLVCAACSVELL. Amino acid analysis, confirmed by H-1-NMR, suggested cerein MRX1 to be a class II bacteriocin. This bacteriocin was remarkably hydrophobic, heat-stable and could withstand a wide range of pH. It exhibited a bactericidal mode of action against Bacillus coagulans JCM 2257(T). Cerein MRX1 was especially active against spoilage bacteria such as Bacillus subtilis and Listeria innocua (MICs in the 1 mu g ml(-1) range). In contrast, lactic acid bacteria were resistant or required higher concentrations to be inhibited. Conclusions: Cerein MRX1 is similar by its N-terminal sequence to thuricin 17 recently isolated from Bacillus thuringiensis NEB17. However, the two bacteriocins are different by their molecular masses and amino acid compositions. Significance and Impact of the Study: Chemical stability of cerein MRX1 and its ability to inhibit a large number of undesirable bacteria may give an advantage to its food or clinical application as an antibacterial agent.
引用
收藏
页码:1621 / 1631
页数:11
相关论文
共 35 条
[1]   EXPANSION OF BACTERIOCIN ACTIVITY AND HOST-RANGE UPON COMPLEMENTATION OF 2 PEPTIDES ENCODED WITHIN THE LACTACIN-F OPERON [J].
ALLISON, GE ;
FREMAUX, C ;
KLAENHAMMER, TR .
JOURNAL OF BACTERIOLOGY, 1994, 176 (08) :2235-2241
[2]   DIRECT DETECTION OF AN ANTIMICROBIAL PEPTIDE OF PEDIOCOCCUS-ACIDILACTICI IN SODIUM DODECYL SULFATE-POLYACRYLAMIDE GEL-ELECTROPHORESIS [J].
BHUNIA, AK ;
JOHNSON, MC ;
RAY, B .
JOURNAL OF INDUSTRIAL MICROBIOLOGY, 1987, 2 (05) :319-322
[3]   Lantibiotics as surface active agents for biomedical applications [J].
Bower, CK ;
Bothwell, MK ;
McGuire, J .
COLLOIDS AND SURFACES B-BIOINTERFACES, 2001, 22 (04) :259-265
[4]   The lantibiotic mersacidin inhibits peptidoglycan synthesis by targeting lipid II [J].
Brötz, H ;
Bierbaum, G ;
Leopold, K ;
Reynolds, PE ;
Sahl, HG .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (01) :154-160
[5]   Molecular mechanism of membrane permeabilization by the peptide antibiotic surfactin [J].
Carrillo, C ;
Teruel, JA ;
Aranda, FJ ;
Ortiz, A .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2003, 1611 (1-2) :91-97
[6]  
Chen HQ, 2003, INT J FOOD MICROBIOL, V87, P161, DOI [10.1111/j.1541-4337.2003.tb00016.x, 10.1016/S0168-1605(03)00064-3]
[7]   Bacteriocins: Developing innate immunity for food [J].
Cotter, PD ;
Hill, C ;
Ross, RP .
NATURE REVIEWS MICROBIOLOGY, 2005, 3 (10) :777-788
[8]   SIMPLE METHOD OF PURIFICATION AND SEQUENCING OF A BACTERIOCIN PRODUCED BY PEDIOCOCCUS-ACIDILACTICI UL5 [J].
DABA, H ;
LACROIX, C ;
HUANG, J ;
SIMARD, RE ;
LEMIEUX, L .
JOURNAL OF APPLIED BACTERIOLOGY, 1994, 77 (06) :682-688
[9]  
DUNN B, 1995, CURRENT PROTOCOLS PR
[10]   Proteomic analysis of the bacteriocin thuricin 17 produced by Bacillus thuringiensis NEB17 [J].
Gray, EJ ;
Di Falco, M ;
Souleimanov, A ;
Smith, DL .
FEMS MICROBIOLOGY LETTERS, 2006, 255 (01) :27-32