Literature DB >> 25085495

ApnI, a transmembrane protein responsible for subtilomycin immunity, unveils a novel model for lantibiotic immunity.

Yun Deng1, Cong-Zhi Li1, Yi-Guang Zhu1, Peng-Xia Wang1, Qing-Dong Qi1, Jing-Jing Fu1, Dong-Hai Peng1, Li-Fang Ruan1, Ming Sun2.   

Abstract

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.
Copyright © 2014, American Society for Microbiology. All Rights Reserved.

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Year:  2014        PMID: 25085495      PMCID: PMC4178640          DOI: 10.1128/AEM.02280-14

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  44 in total

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Authors:  A Krogh; B Larsson; G von Heijne; E L Sonnhammer
Journal:  J Mol Biol       Date:  2001-01-19       Impact factor: 5.469

2.  REQUIREMENTS FOR TRANSFORMATION IN BACILLUS SUBTILIS.

Authors:  C Anagnostopoulos; J Spizizen
Journal:  J Bacteriol       Date:  1961-05       Impact factor: 3.490

3.  Molecular analysis of expression of the lantibiotic pep5 immunity phenotype.

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Journal:  Appl Environ Microbiol       Date:  1999-02       Impact factor: 4.792

4.  Structural and functional diversity of lantibiotic immunity proteins.

Authors:  Ken-ichi Okuda; Kenji Sonomoto
Journal:  Curr Pharm Biotechnol       Date:  2011-08       Impact factor: 2.837

5.  Draft genome sequence of the Paenibacillus polymyxa type strain (ATCC 842T), a plant growth-promoting bacterium.

Authors:  Haeyoung Jeong; Soo-Young Park; Won-Hyong Chung; Sun Hong Kim; Namshin Kim; Seung-Hwan Park; Jihyun F Kim
Journal:  J Bacteriol       Date:  2011-07-08       Impact factor: 3.490

6.  Characterization of the nisin gene cluster nisABTCIPR of Lactococcus lactis. Requirement of expression of the nisA and nisI genes for development of immunity.

Authors:  O P Kuipers; M M Beerthuyzen; R J Siezen; W M De Vos
Journal:  Eur J Biochem       Date:  1993-08-15

7.  Studies on transformation of Escherichia coli with plasmids.

Authors:  D Hanahan
Journal:  J Mol Biol       Date:  1983-06-05       Impact factor: 5.469

8.  Regulation of the Bacillus subtilis bcrC bacitracin resistance gene by two extracytoplasmic function sigma factors.

Authors:  Min Cao; John D Helmann
Journal:  J Bacteriol       Date:  2002-11       Impact factor: 3.490

9.  Relatedness between the two-component lantibiotics lacticin 3147 and staphylococcin C55 based on structure, genetics and biological activity.

Authors:  Eileen B O'Connor; Paul D Cotter; Paula O'Connor; Orla O'Sullivan; John R Tagg; R Paul Ross; Colin Hill
Journal:  BMC Microbiol       Date:  2007-04-02       Impact factor: 3.605

Review 10.  Structure, function, and biology of the Enterococcus faecalis cytolysin.

Authors:  Daria Van Tyne; Melissa J Martin; Michael S Gilmore
Journal:  Toxins (Basel)       Date:  2013-04-29       Impact factor: 4.546

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Authors:  Bingyue Xin; Jinshui Zheng; Ziya Xu; Congzhi Li; Lifang Ruan; Donghai Peng; Ming Sun
Journal:  Appl Environ Microbiol       Date:  2015-07-31       Impact factor: 4.792

2.  The Bacillus cereus group is an excellent reservoir of novel lanthipeptides.

Authors:  Bingyue Xin; Jinshui Zheng; Ziya Xu; Xiaoling Song; Lifang Ruan; Donghai Peng; Ming Sun
Journal:  Appl Environ Microbiol       Date:  2014-12-29       Impact factor: 4.792

Review 3.  Emerging concepts promising new horizons for marine biodiscovery and synthetic biology.

Authors:  F Jerry Reen; José A Gutiérrez-Barranquero; Alan D W Dobson; Claire Adams; Fergal O'Gara
Journal:  Mar Drugs       Date:  2015-05-13       Impact factor: 5.118

4.  Endophyte Bacillus subtilis evade plant defense by producing lantibiotic subtilomycin to mask self-produced flagellin.

Authors:  Yun Deng; Hanqiao Chen; Congzhi Li; Jianyi Xu; Qingdong Qi; Yuanyuan Xu; Yiguang Zhu; Jinshui Zheng; Donghai Peng; Lifang Ruan; Ming Sun
Journal:  Commun Biol       Date:  2019-10-10

5.  Three novel leaderless bacteriocins have antimicrobial activity against gram-positive bacteria to serve as promising food biopreservative.

Authors:  Xiaofeng Zhang; Nie Xin; Zhaolu Zhu; Xudong Li; Dadong Dai; Chunmei Pan; Donghai Peng; Ming Sun
Journal:  Microb Cell Fact       Date:  2022-09-19       Impact factor: 6.352

  5 in total

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