Natural Product Biosynthetic Gene Diversity in Geographically Distinct Soil Microbiomes

被引:77
作者
Reddy, Boojala Vijay B. [1 ]
Kallifidas, Dimitris [1 ]
Kim, Jeffrey H. [1 ]
Charlop-Powers, Zachary [1 ]
Feng, Zhiyang [1 ]
Brady, Sean F. [1 ]
机构
[1] Rockefeller Univ, Howard Hughes Med Inst, Lab Genetically Encoded Small Mol, New York, NY 10021 USA
关键词
MULTIPLE SEQUENCE ALIGNMENT; HETEROLOGOUS EXPRESSION; DNA; POLYKETIDE; CLONING; CLUSTERS; MICROORGANISMS; BIOGEOGRAPHY; ANTIBIOTICS; SENSITIVITY;
D O I
10.1128/AEM.00102-12
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
The number of bacterial species estimated to exist on Earth has increased dramatically in recent years. This newly recognized species diversity has raised the possibility that bacterial natural product biosynthetic diversity has also been significantly underestimated by previous culture-based studies. Here, we compare 454-pyrosequenced nonribosomal peptide adenylation domain, type I polyketide ketosynthase domain, and type II polyketide ketosynthase alpha gene fragments amplified from cosmid libraries constructed using DNA isolated from three different arid soils. While 16S rRNA gene sequence analysis indicates these cloned metagenomes contain DNA from similar distributions of major bacterial phyla, we found that they contain almost completely distinct collections of secondary metabolite biosynthetic gene sequences. When grouped at 85% identity, only 1.5% of the adenylation domain, 1.2% of the ketosynthase, and 9.3% of the ketosynthase alpha sequence clusters contained sequences from all three metagenomes. Although there is unlikely to be a simple correlation between biosynthetic gene sequence diversity and the diversity of metabolites encoded by the gene clusters in which these genes reside, our analysis further suggests that sequences in one soil metagenome are so distantly related to sequences in another metagenome that they are, in many cases, likely to arise from functionally distinct gene clusters. The marked differences observed among collections of biosynthetic genes found in even ecologically similar environments suggest that prokaryotic natural product biosynthesis diversity is, like bacterial species diversity, potentially much larger than appreciated from culture-based studies.
引用
收藏
页码:3744 / 3752
页数:9
相关论文
共 37 条
  • [1] New PCR primers for the screening of NRPS and PKS-I systems in actinomycetes: Detection and distribution of these biosynthetic gene sequences in major taxonomic groups
    Ayuso-Sacido, A
    Genilloud, O
    [J]. MICROBIAL ECOLOGY, 2005, 49 (01) : 10 - 24
  • [2] Cloning and characterization of new glycopeptide gene clusters found in an environmental DNA megalibrary
    Banik, Jacob J.
    Brady, Sean F.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (45) : 17273 - 17277
  • [3] Tailoring Enzyme-Rich Environmental DNA Clones: A Source of Enzymes for Generating Libraries of Unnatural Natural Products
    Banik, Jacob J.
    Craig, Jeffrey W.
    Calle, Paula Y.
    Brady, Sean F.
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (44) : 15661 - 15670
  • [4] Beijerinck MW, 1913, KONINKLIJKE JB
  • [5] Construction of soil environmental DNA cosmid libraries and screening for clones that produce biologically active small molecules
    Brady, Sean F.
    [J]. NATURE PROTOCOLS, 2007, 2 (05) : 1297 - 1305
  • [6] Cloning and Characterization of an Environmental DNA-Derived Gene Cluster That Encodes the Biosynthesis of the Antitumor Substance BE-54017
    Chang, Fang-Yuan
    Brady, Sean F.
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2011, 133 (26) : 9996 - 9999
  • [7] ESTIMATING THE POPULATION-SIZE FOR CAPTURE RECAPTURE DATA WITH UNEQUAL CATCHABILITY
    CHAO, A
    [J]. BIOMETRICS, 1987, 43 (04) : 783 - 791
  • [8] Comparison of two next-generation sequencing technologies for resolving highly complex microbiota composition using tandem variable 16S rRNA gene regions
    Claesson, Marcus J.
    Wang, Qiong
    O'Sullivan, Orla
    Greene-Diniz, Rachel
    Cole, James R.
    Ross, R. Paul
    O'Toole, Paul W.
    [J]. NUCLEIC ACIDS RESEARCH, 2010, 38 (22) : e200
  • [9] New antibiotics from bacterial natural products
    Clardy, Jon
    Fischbach, Michael A.
    Walsh, Christopher T.
    [J]. NATURE BIOTECHNOLOGY, 2006, 24 (12) : 1541 - 1550
  • [10] The Ribosomal Database Project: improved alignments and new tools for rRNA analysis
    Cole, J. R.
    Wang, Q.
    Cardenas, E.
    Fish, J.
    Chai, B.
    Farris, R. J.
    Kulam-Syed-Mohideen, A. S.
    McGarrell, D. M.
    Marsh, T.
    Garrity, G. M.
    Tiedje, J. M.
    [J]. NUCLEIC ACIDS RESEARCH, 2009, 37 : D141 - D145