Purification and partial identification of bacteriocin ISK-1, a new lantibiotic produced by Pediococcus sp. ISK-1

被引:33
作者
Kimura, H [1 ]
Matsusaki, H [1 ]
Sashihara, T [1 ]
Sonomoto, K [1 ]
Ishizaki, A [1 ]
机构
[1] Kyushu Univ, Fac Agr, Dept Food Sci & Technol, Lab Microbial Technol,Higashi Ku, Fukuoka 8128581, Japan
关键词
Pediococcus; bacteriocin; lantibiotic; Nukadoko;
D O I
10.1271/bbb.62.2341
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
Bacteriocin ISK-1 is a proteinaceous inhibitory substance produced by Pediococcus sp. ISK-1 isolated from well-aged Nukadoko. Bacteriocin ISK-1 was purified by acid treatment, ammonium sulfate precipitation, cation-exchange chromatography, and reversed-phase HPLC from the culture supernatant of Pediococcus sp. ISK-1. Purification of bacteriocin ISK-1 resulted in a 30-fold increase in the specific activity and the recovery was 17%. Molecular mass of bacteriocin ISK-1 measured by fast atom bombardment-mass spectrometry was 2,960. The amino acid composition analysis of bacteriocin ISK-1 showed that it contained unusual amino acids such as lanthionine and/or 3-methyllanthionine, which is a characteristic of lantibiotics. The N-terminal amino acid sequence analysis indicated the first seven N-terminal amino acid residues as NH2-K-K-K-S-G-V-I. The primary sequence showed significant similarity to the lantibiotics lacticin 481 from Lactococcus lactis and variacin from Micrococcus varians, which suggests that bacteriocin ISK-1 is a novel lantibiotic belonging to a lacticin-481 type.
引用
收藏
页码:2341 / 2345
页数:5
相关论文
共 36 条
[1]   EPIDERMIN - SEQUENCING OF A HETERODET TETRACYCLIC 21-PEPTIDE AMIDE ANTIBIOTIC [J].
ALLGAIER, H ;
JUNG, G ;
WERNER, RG ;
SCHNEIDER, U ;
ZAHNER, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1986, 160 (01) :9-22
[2]   Engineering of a novel thioether bridge and role of modified residues in the lantibiotic pep5 [J].
Bierbaum, G ;
Szekat, C ;
Josten, M ;
Heidrich, C ;
Kempter, C ;
Jung, G ;
Sahl, HG .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (02) :385-392
[3]   A NOVEL POSTTRANSLATIONAL MODIFICATION OF THE PEPTIDE ANTIBIOTIC SUBTILIN - ISOLATION AND CHARACTERIZATION OF A NATURAL VARIANT FROM BACILLUS-SUBTILIS ATCC-6633 [J].
CHAN, WC ;
BYCROFT, BW ;
LEYLAND, ML ;
LIAN, LY ;
ROBERTS, GCK .
BIOCHEMICAL JOURNAL, 1993, 291 :23-27
[4]  
DELVESBROUGHTON J, 1990, FOOD TECHNOL-CHICAGO, V44, P100
[5]   GENETIC-STRUCTURE OF THE ENTEROCOCCUS-FAECALIS PLASMID PAD1-ENCODED CYTOLYTIC TOXIN SYSTEM AND ITS RELATIONSHIP TO LANTIBIOTIC DETERMINANTS [J].
GILMORE, MS ;
SEGARRA, RA ;
BOOTH, MC ;
BOGIE, CP ;
HALL, LR ;
CLEWELL, DB .
JOURNAL OF BACTERIOLOGY, 1994, 176 (23) :7335-7344
[6]   STRUCTURE OF NISIN [J].
GROSS, E ;
MORELL, JL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1971, 93 (18) :4634-+
[7]   THE LEADER PEPTIDE OF COLICIN-V SHARES CONSENSUS SEQUENCES WITH LEADER PEPTIDES THAT ARE COMMON AMONG PEPTIDE BACTERIOCINS PRODUCED BY GRAM-POSITIVE BACTERIA [J].
HAVARSTEIN, LS ;
HOLO, H ;
NES, IF .
MICROBIOLOGY-SGM, 1994, 140 :2383-2389
[8]   Optimization of the culture medium for growth and the kinetics of lactate fermentation by Pediococcus sp. ISK-1 [J].
Herawaiti, E ;
Ishizaki, A .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 1997, 61 (04) :604-608
[9]  
Herawati E, 1998, J FAC AGR KYUSHU U, V42, P449
[10]   DUPLICATION OF THE LANTIBIOTIC STRUCTURAL GENE IN M-TYPE-49 GROUP-A STREPTOCOCCUS STRAINS PRODUCING STREPTOCOCCIN-A-M49 [J].
HYNES, WL ;
FRIEND, VL ;
FERRETTI, JJ .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1994, 60 (11) :4207-4209