Complete genome sequence and comparative genomic analyses of the vancomycin-producing Amycolatopsis orientalis

被引:57
|
作者
Xu, Li [1 ,2 ]
Huang, He [3 ]
Wei, Wei [2 ]
Zhong, Yi [3 ]
Tang, Biao [4 ,5 ]
Yuan, Hua [3 ]
Zhu, Li [2 ]
Huang, Weiyi [1 ]
Ge, Mei [2 ]
Yang, Shen [3 ]
Zheng, Huajun [6 ]
Jiang, Weihong [3 ]
Chen, Daijie [2 ,7 ]
Zhao, Guo-Ping [3 ,4 ,5 ,6 ,8 ,9 ]
Zhao, Wei [3 ,4 ,5 ,10 ,11 ]
机构
[1] Nanjing Agr Univ, Nanjing 210095, Jiangsu, Peoples R China
[2] Shanghai Laiyi Ctr Biopharmaceut R&D, Shanghai 200240, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Plant Physiol & Ecol, CAS Key Lab Synthet Biol, Shanghai 200031, Peoples R China
[4] Fudan Univ, Sch Life Sci, Dept Microbiol, State Key Lab Genet Engn, Shanghai 200433, Peoples R China
[5] Fudan Univ, Inst Biomed Sci, Shanghai 200433, Peoples R China
[6] Chinese Natl Human Genome Ctr, Shanghai MOST Key Lab Dis & Hlth Genom, Shanghai 201203, Peoples R China
[7] Shanghai Inst Pharmaceut Ind, Shanghai 200040, Peoples R China
[8] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Microbiol, Shatin, Hong Kong, Peoples R China
[9] Chinese Univ Hong Kong, Prince Wales Hosp, Li Ka Shing Inst Hlth Sci, Shatin, Hong Kong, Peoples R China
[10] China HKY Gene Technol Co Ltd, Shenzhen 518057, Guangdong, Peoples R China
[11] Shenzhen Univ, Coll Med, Shenzhen 518060, Guangdong, Peoples R China
来源
BMC GENOMICS | 2014年 / 15卷
基金
中国国家自然科学基金;
关键词
Amycolatopsis orientalis; Complete genome sequencing; Molecular taxonomic characteristics; Vancomycin biosynthesis; RESISTANT STAPHYLOCOCCUS-AUREUS; GLYCOPEPTIDE ANTIBIOTICS; ESCHERICHIA-COLI; BIOSYNTHETIC-PATHWAY; MEDITERRANEI DSM5908; AMINO-ACID; CHLOROEREMOMYCIN; ACTINOMYCETE; GENES; CYTOCHROME-P450;
D O I
10.1186/1471-2164-15-363
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
Background: Amycolatopsis orientalis is the type species of the genus and its industrial strain HCCB10007, derived from ATCC 43491, has been used for large-scale production of the vital antibiotic vancomycin. However, to date, neither the complete genomic sequence of this species nor a systemic characterization of the vancomycin biosynthesis cluster (vcm) has been reported. With only the whole genome sequence of Amycolatopsis mediterranei available, additional complete genomes of other species may facilitate intra-generic comparative analysis of the genus. Results: The complete genome of A. orientalis HCCB10007 comprises an 8,948,591-bp circular chromosome and a 33,499-bp dissociated plasmid. In total, 8,121 protein-coding sequences were predicted, and the species-specific genomic features of A. orientalis were analyzed in comparison with that of A. mediterranei. The common characteristics of Amycolatopsis genomes were revealed via intra-and inter-generic comparative genomic analyses within the domain of actinomycetes, and led directly to the development of sequence-based Amycolatopsis molecular chemotaxonomic characteristics (MCCs). The chromosomal core/quasi-core and non-core configurations of the A. orientalis and the A. mediterranei genome were analyzed reciprocally, with respect to further understanding both the discriminable criteria and the evolutionary implementation. In addition, 26 gene clusters related to secondary metabolism, including the 64-kb vcm cluster, were identified in the genome. Employing a customized PCR-targeting-based mutagenesis system along with the biochemical identification of vancomycin variants produced by the mutants, we were able to experimentally characterize a halogenase, a methyltransferase and two glycosyltransferases encoded in the vcm cluster. The broad substrate spectra characteristics of these modification enzymes were inferred. Conclusions: This study not only extended the genetic knowledge of the genus Amycolatopsis and the biochemical knowledge of vcm-related post-assembly tailoring enzymes, but also developed methodology useful for in vivo studies in A. orientalis, which has been widely considered as a barrier in this field.
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页数:18
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