ApnI, a Transmembrane Protein Responsible for Subtilomycin Immunity, Unveils a Novel Model for Lantibiotic Immunity

被引:11
|
作者
Deng, Yun [1 ]
Li, Cong-Zhi [1 ]
Zhu, Yi-Guang [1 ]
Wang, Peng-Xia [1 ]
Qi, Qing-Dong [1 ]
Fu, Jing-Jing [1 ]
Peng, Dong-Hai [1 ]
Ruan, Li-Fang [1 ]
Sun, Ming [1 ]
机构
[1] Huazhong Agr Univ, Coll Life Sci & Technol, State Key Lab Agr Microbiol, Wuhan, Peoples R China
基金
中国国家自然科学基金;
关键词
ENTEROCOCCUS-FAECALIS CYTOLYSIN; STAPHYLOCOCCUS-WARNERI ISK-1; BIOSYNTHETIC GENE-CLUSTER; BACILLUS-SUBTILIS; LACTOCOCCUS-LACTIS; FUNCTIONAL-ANALYSIS; PRODUCER IMMUNITY; NUKACIN ISK-1; EXPRESSION; RESISTANCE;
D O I
10.1128/AEM.02280-14
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
Subtilomycin was detected from the plant endophytic strain Bacillus subtilis BSn5 and was first reported from B. subtilis strain MMA7. In this study, a gene cluster that has been proposed to be related to subtilomycin biosynthesis was isolated from the BSn5 genome and was experimentally validated by gene inactivation and heterologous expression. Comparison of the subtilomycin gene cluster with other verified related lantibiotic gene clusters revealed a particular organization of the genes apnI and apnT downstream of apnAPBC, which may be involved in subtilomycin immunity. Through analysis of expression of the apnI and/or apnT genes in the subtilomycin-sensitive strain CU1065 and inactivation of apnI and apnT in the producer strain BSn5, we showed that the single gene apnI, encoding a putative transmembrane protein, was responsible for subtilomycin immunity. To our knowledge, evidence for lantibiotic immunity that is solely dependent on a transmembrane protein is quite rare. Further bioinformatic analysis revealed the abundant presence of ApnI-like proteins that may be responsible for lantibiotic immunity in Bacillus and Paenibacillus. We cloned the paeI gene, encoding one such ApnI-like protein, into CU1065 and showed that it confers resistance to paenibacillin. However, no cross-resistance was detected between ApnI and PaeI, even though subtilomycin and paenibacillin share similar structures, suggesting that the protection provided by ApnI/ApnI-like proteins involves a specific-sequence recognition mechanism. Peptide release/binding assays indicated that the recombinant B. subtilis expressing apnI interacted with subtilomycin. Thus, ApnI represents a novel model for lantibiotic immunity that appears to be common.
引用
收藏
页码:6303 / 6315
页数:13
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