A novel type of immunity protein, Nuk-R, for the lantibiotic nukacin ISK-1 produced by Staphylococcus warneri ISK-1

被引:43
作者
Aso, Y
Okuda, K
Nagao, J
Kanemasa, Y
Phuong, NTB
Koga, H
Shioya, K
Sashihara, T
Nakayama, J
Sonomoto, K
机构
[1] Kyushu Univ, Grad Sch,Fac Agr, Dept Biosci & Biotechnol,Lab Microbial Technol, Div Microbial Sci & Technol,Higashi Ku, Fukuoka 8128581, Japan
[2] Kyushu Univ, Dept Funct Metab Design, Bioarchitecture Ctr, Lab Funct Food Design,Higashi Ku, Fukuoka 8128581, Japan
基金
日本学术振兴会;
关键词
lantibiotic; bacteriocin; nukacin ISK-1; Staphylococcus; immunity;
D O I
10.1271/bbb.69.1403
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
Staphylococcus warneri ISK-1 produces a lantibiotic, nukacin ISK-1. The nukacin ISK-1 gene cluster consists of at least six genes, nukA, -M, -T, -F, -E, and -G, and two open reading frames, ORF1 and ORF7 (designated nukH). Sequence comparisons suggested that NukF, -E, -G, and -H contribute to immunity to nukacin ISK-1. We investigated the immunity levels of recombinant Lactococcus lactis expressing nukFEG and nukH against nukacin ISK-1. The co-expression of nukFEG and nukH resulted in a high degree of immunity. The expression of either nukFEG or nukH conferred partial immunity against nukacin ISK-1. These results suggest that NukH contributes cooperatively to self-protection with NukFEG. The nukacin ISK-1 immunity system might function against another antibiotic, lacticin 481. Western blot analysis showed that NukH expressed in Staphylococcus carnosus was localized in the membrane. Peptide release/bind assays indicated that the recombinant L. lactis expressing nukH interacted with nukacin ISK-1 and lacticin 481 but not with nisin A. These findings suggest that NukH contributes cooperatively to host immunity as a novel type of lantibiotic-binding immunity protein with NukFEG.
引用
收藏
页码:1403 / 1410
页数:8
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