Liu Gang, Zhong Jin, Ni Jianqiang, Chen Meiling, Xiao Haijie, Huan Liandong
Graduate University of Chinese Academy of Sciences, Beijing 100039, PR China.
State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, PR China.
Microbiology (Reading). 2009 Feb;155(Pt 2):584-593. doi: 10.1099/mic.0.022707-0.
Bovicin HJ50 is a new lantibiotic containing a disulfide bridge produced by Streptococcus bovis HJ50; its encoding gene bovA was reported in our previous publication. To identify other genes involved in bovicin HJ50 production, DNA fragments flanking bovA were cloned and sequenced. The bovicin HJ50 biosynthesis gene locus was encoded by a 9.9 kb region of chromosomal DNA and consisted of at least nine genes in the following order: bovA, -M, -T, -E, -F, ORF1, ORF2, bovK and bovR. A thiol-disulfide oxidoreductase gene named sdb1 was located downstream of bovR. A knockout mutant of this gene retained antimicrobial activity and the molecular mass of bovicin HJ50 in the mutant was the same as that of bovicin HJ50 in S. bovis HJ50, implying that sdb1 is not involved in bovicin HJ50 production. Transcriptional analyses showed that bovA, bovM and bovT constituted an operon, and the transcription start site of the bovA promoter was located at a G residue 45 bp upstream of the translation start codon for bovA, while bovE through bovR were transcribed together and the transcription start site of the bovE promoter was located at a C residue 35 bp upstream of bovE. We also demonstrated successful heterologous expression of bovicin HJ50 in Lactococcus lactis MG1363, which lacks thiol-disulfide oxidoreductase genes; this showed that thiol-disulfide oxidoreductase genes other than sdb1 are not essential for bovicin HJ50 biosynthesis.
博维菌素HJ50是一种由牛链球菌HJ50产生的含有二硫键的新型羊毛硫抗生素;其编码基因bovA在我们之前的出版物中已有报道。为了鉴定参与博维菌素HJ50产生的其他基因,对bovA侧翼的DNA片段进行了克隆和测序。博维菌素HJ50生物合成基因座由染色体DNA的一个9.9 kb区域编码,至少由九个基因按以下顺序组成:bovA、-M、-T、-E、-F、开放阅读框1、开放阅读框2、bovK和bovR。一个名为sdb1的硫醇-二硫键氧化还原酶基因位于bovR的下游。该基因的敲除突变体保留了抗菌活性,并且突变体中博维菌素HJ50的分子量与牛链球菌HJ50中博维菌素HJ50的分子量相同,这意味着sdb1不参与博维菌素HJ50的产生。转录分析表明,bovA、bovM和bovT构成一个操纵子,bovA启动子的转录起始位点位于bovA翻译起始密码子上游45 bp处的一个G残基,而bovE至bovR一起转录,bovE启动子的转录起始位点位于bovE上游35 bp处的一个C残基。我们还证明了博维菌素HJ50在缺乏硫醇-二硫键氧化还原酶基因的乳酸乳球菌MG1363中的成功异源表达;这表明除sdb1之外的硫醇-二硫键氧化还原酶基因对于博维菌素HJ50的生物合成不是必需的。