Genetic analysis of polyketide synthase and peptide synthetase genes in cyanobacteria as a mining tool for secondary metabolites

被引:46
作者
Barrios-Llerena, Martin E.
Burja, Adam M.
Wright, Phillip C.
机构
[1] Univ Sheffield, Dept Chem & Proc Engn, Biol & Environm Syst Grp, Sheffield S1 3JD, S Yorkshire, England
[2] Ocean Nutr Canada, Metab Engn & Fermentat Grp, Dartmouth, NS B2Y 4T6, Canada
基金
英国工程与自然科学研究理事会;
关键词
peptide synthetases; polyketide synthases; cyanobacteria; ketosynthase domain; adenylation domain; natural products;
D O I
10.1007/s10295-007-0216-6
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
Molecular screening using degenerate PCR to determine the presence of secondary metabolite genes in cyanobacteria was performed. This revealed 18 NRPS and 19 PKS genes in the 21 new cyanobacterial strains examined, representing three families of cyanobacteria (Nostocales, Chroococales and Oscillatoriales). A BLAST analysis shows that these genes have similarities to known cyanobacterial natural products. Analysis of the NRPS adenylation domain indicates the presence of novel features previously ascribed to both proteobacteria and cyanobacteria. Furthermore, binding-pocket predictions reveal diversity in the amino acids used during the biosynthesis of compounds. A similar analysis of the PKS ketosynthase domain shows significant structural diversity and their presence in both mixed modules with NRPS domains and individually as part of a PKS module. We have been able to classify the NRPS genes on the basis of their binding-pockets. Further, we show how this data can be used to begin to link structure to function by an analysis of the compounds Scyptolin A and Hofmannolin from Scytonema sp. PCC 7110.
引用
收藏
页码:443 / 456
页数:14
相关论文
共 74 条
  • [1] BASIC LOCAL ALIGNMENT SEARCH TOOL
    ALTSCHUL, SF
    GISH, W
    MILLER, W
    MYERS, EW
    LIPMAN, DJ
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) : 403 - 410
  • [2] [Anonymous], 1989, Molecular Cloning
  • [3] Nostocarboline:: Isolation and synthesis of a new cholinesterase inhibitor from Nostoc 78-12A
    Becher, PG
    Beuchat, J
    Gademann, K
    Jüttner, F
    [J]. JOURNAL OF NATURAL PRODUCTS, 2005, 68 (12): : 1793 - 1795
  • [4] Evaluation of Nostoc strain ATCC 53789 as a potential source of natural pesticides
    Biondi, N
    Piccardi, R
    Margheri, MC
    Rodolfi, L
    Smith, GD
    Tredici, MR
    [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (06) : 3313 - 3320
  • [5] MICROALGAE AS SOURCES OF PHARMACEUTICALS AND OTHER BIOLOGICALLY-ACTIVE COMPOUNDS
    BOROWITZKA, MA
    [J]. JOURNAL OF APPLIED PHYCOLOGY, 1995, 7 (01) : 3 - 15
  • [6] Marine cyanobacteria - a prolific source of natural products
    Burja, AM
    Banaigs, B
    Abou-Mansour, E
    Burgess, JG
    Wright, PC
    [J]. TETRAHEDRON, 2001, 57 (46) : 9347 - 9377
  • [7] Microbial diversity of extant stromatolites in the hypersaline marine environment of Shark Bay, Australia
    Burns, BP
    Goh, F
    Allen, M
    Neilan, BA
    [J]. ENVIRONMENTAL MICROBIOLOGY, 2004, 6 (10) : 1096 - 1101
  • [8] The parallel and convergent universes of polyketide synthases and nonribosomal peptide synthetases
    Cane, DE
    Walsh, CT
    [J]. CHEMISTRY & BIOLOGY, 1999, 6 (12): : R319 - R325
  • [9] Coelichelin, a new peptide siderophore encoded by the Streptomyces coelicolor genome:: structure prediction from the sequence of its non-ribosomal peptide synthetase
    Challis, GL
    Ravel, J
    [J]. FEMS MICROBIOLOGY LETTERS, 2000, 187 (02) : 111 - 114
  • [10] Predictive, structure-based model of amino acid recognition by nonribosomal peptide synthetase adenylation domains
    Challis, GL
    Ravel, J
    Townsend, CA
    [J]. CHEMISTRY & BIOLOGY, 2000, 7 (03): : 211 - 224