期刊文献+

海洋稀有放线菌Salinispora arenicola CNP193基因组新颖PKS和NRPS基因簇的发掘 被引量:5

Mining Salinispora arenicola CNP193 genome for novel PKS and NRPS gene clusters
在线阅读 下载PDF
导出
摘要 利用基因组发掘技术,从海洋稀有放线菌Salinispora arenicola CNP193基因组序列中发掘新颖PKS和NRPS基因簇,并初步预测基因簇对应产物,为新颖聚酮化合物的发现,基因簇的异源表达和利用组合生物合成技术对化合物结构进行改造提供信息。在利用anti SMASH对S.arenicola CNS 205和S.arenicola CNP193次级代谢产物基因簇进行预测,并经过NRPS-PKS knowledgebase验证的基础上,以S.arenicola CNS 205基因簇为对照,初步选择新颖基因簇;进一步用NCBI Blast和Nap Dos分析判断基因簇的新颖性后获得3个新颖基因簇:基因簇7,基因簇10和基因簇20。结合anti SMASH对基因簇核心结构的预测和与已知功能同源性基因簇,NCBI Blast比对的同源序列,以及Nap Dos对个基因簇中KS domain和C domain的进化分析等信息,初步表明基因簇7和基因簇20的对应产物分别为烯二炔类和有半胱氨酸及其他氨基酸参与合成的肽类化合物。由于基因簇10得到的信息较少,不能预测其代谢产物。 Novel polyketide synthases (PKS) and non-ribosomal peptide synthetases (NRPS) gene clusters were mined from the genome of the obligate marine actinomycete strain S. arenicola CNP193 through bioinformatics analysis. The metabolic products of the gene clusters were predicted based on the bioinformatics analysis, which would lay an experimental base for discovery of novel polyketides, heterologous expression of the gene clusters, and modification of the product through combinatorial biosynthesis. The genome sequences of S. arenicola CNP 193 and S. arenicola CNS 205 were scanned for potential PKS and NRPS modular clusters with antiSMASH and NRPS-PKS knowledgebase. The potential novel PKS and NRPS gene clusters from the chromosome of the S. arenicola CNP193 were selected with that of the S. arenicola CNS 193 as control. Three novel PKS and NRPS gene clusters, named gene cluster 7, gene cluster 10, and gene cluster 20, were selected after analyzed by NCBI Blast and NapDos. The products of the gene clusters were predicted by combination all the hints from the analysis results of antiSMASH, NCBI Blast, and NapDos. The metabolic products of gene cluster 7 and gene cluster 20 would be enediyne and peptide respectively, and cysteine was one of the amino acid compositions of the peptide. However, the metabolic product of gene cluster 20 couldn't be predicted based on the information acquired.
出处 《海洋科学》 CAS CSCD 北大核心 2014年第12期48-57,共10页 Marine Sciences
基金 中央财政支持地方高校发展专项资金资助项目(CXTD13) 江苏省自然科学基金项目(BK20141249) 江苏省高校自然科学研究项目(13KJB550003) 江苏省2014年度青蓝工程项目第48批"留学回国人员"科研启动基金
关键词 基因簇发掘 新颖PKS基因簇 新颖NRPS基因簇 产物预测 Genome mining novel PKS gene cluster novel NRPS gene cluster prediction of metabolic product
  • 相关文献

参考文献26

  • 1Winter J M, Tang Y. Synthetic biological approaches to natural product biosynthesis[J]. Current Opinion in Biotechnology, 2012, 23: 736-743.
  • 2杨建,洪葵.宏基因组文库技术获得聚酮化合物[J].遗传,2006,28(10):1330-1336. 被引量:12
  • 3Manivasagan P, Venkatesan J, Sivakumar K, et al. Marine actinobacterial metabolites: current status andfuture perspectives[J]. Microbiological Research, 2013, 168: 311-332.
  • 4Oman T J, van der Donk W A. Follow the leader: the use of leader peptides to guide natural product biosyn- thesis[J]. Nature Chemical Biology, 2010, 6:9-18.
  • 5Lane A L, Moore B S. A sea of biosynthesis: marine natural products meet the molecular age[J]. Natural Product Reports, 2011, 28: 411-428.
  • 6Kersten R D, Yang Y L, Xu Y, et al. A mass spectro- metry-guided genome mining approach for natural product peptidogenomics[J]. Nature Chemical Biology, 2012, 7: 794-802.
  • 7Bentley S D, Chater K F, Cerdeno-Tarraga A M, et al. Complete genome sequence of the model actinomycete Streptomyces coelicolor A3(2) [J]. Nature, 2002, 417: 141-147.
  • 8Udwary D W, Zeigler L, Asolkar R N, et al. Genome sequencing reveals complex secondary metabolome in the marine actinomycete Salinispora tropica[J]. Proce- edings of the National Academy of Sciences, 2007, 104 10376-10381.
  • 9Ziemert, N, Podell S, Penn K, et al. The natural product domain seeker NaPDoS: a phylogeny based bioinformatic tool to classify secondary metabolite gene diversity[J]. PloS One, 2012, 7: e34064.
  • 10Blin K, Medema M H, Kazempour D, et al. antiSMASH 2.0--a versatile platform for genome mining of seco- ndary metabolite producers[J]. Nucleic Acids Research, 2013, 21: 204-212.

二级参考文献93

  • 1阎冰,洪葵,许云,马超.宏基因组克隆——微生物活性物质筛选的新途径[J].微生物学通报,2005,32(1):113-117. 被引量:38
  • 2孙宇辉,邓子新.聚酮化合物及其组合生物合成[J].中国抗生素杂志,2006,31(1):6-14. 被引量:26
  • 3Funa N,Ohnishi Y,Fujii I,et al.A new pathway for polyketide synthesis in microorganisms.Nature,1999,400:897-899.
  • 4Kham N H,Roets E,Hoogmartens J,et al.Quantitative analysis of oxytetracycline and related substances by high-performance liquid chromatography.J.Chrom atogr,1987,405:229-45.
  • 5Mootz H D,Schwatzer D,Marahiel M A.Ways of Assembling Complex Natural Products on Modular Nonribosomal Peptide Synthetases.ChemBioChem,2002,3:490-504.
  • 6连云阳,程元荣.杂合NRPS-PKS的研究进展.//:中国药学会抗生素专业委员会.创新药物及新品种研究、开发学术研讨会论文集.烟台,2006:19-25.
  • 7Menzella H G,Reid R,Carney J R,et al.Combinatorial polyketide biosynthesis by de novo design and rearrangement of modular polyketide synthase genes.Nature Biotechnol,2005,23:1171-1176.
  • 8Doekel S,Marahiel M A.Dipeptide formation on engineered hybrid peptide synthetases.Chem Biol,2000,7(6):373-384.
  • 9Gokhale R S,Tsuji S Y,Cane D E,et al.Dissecting and exploiting intermodular communication in polyketide synthases.Science,1999,284:482-485.
  • 10McDaniel R,Thamchaipenet A,Gustafsson C,et al.Multiple genetic modifications of the erythromycin polyketide synthase to produce a library of novel "unnatural" natural products.Proc Nati Acad,1999,96:1846-1851.

共引文献19

同被引文献39

引证文献5

二级引证文献12

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部