Small molecule in situ resin capture provides a compound first approach to natural product discovery

被引:4
作者
Bogdanov, Alexander [1 ]
Salib, Mariam N. [2 ]
Chase, Alexander B. [1 ,3 ]
Hammerlindl, Heinz [4 ]
Muskat, Mitchell N. [1 ]
Luedtke, Stephanie [5 ]
da Silva, Elany Barbosa [5 ]
O'Donoghue, Anthony J. [5 ]
Wu, Lani F. [4 ]
Altschuler, Steven J. [4 ]
Molinski, Tadeusz F. [2 ]
Jensen, Paul R. [1 ]
机构
[1] Univ Calif San Diego, Scripps Inst Oceanog, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
[3] Southern Methodist Univ, Dept Earth Sci, Dallas, TX 75275 USA
[4] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94158 USA
[5] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
MICROBIAL GENOMES; MASS-SPECTROMETRY; CELL-LINES; DERIVATIVES; DIVERSITY; DIKETOPIPERAZINE; BIOSYNTHESIS; POLYKETIDES; METABOLITES; ACTIVATION;
D O I
10.1038/s41467-024-49367-x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Culture-based microbial natural product discovery strategies fail to realize the extraordinary biosynthetic potential detected across earth's microbiomes. Here we introduce Small Molecule In situ Resin Capture (SMIRC), a culture-independent method to obtain natural products directly from the environments in which they are produced. We use SMIRC to capture numerous compounds including two new carbon skeletons that were characterized using NMR and contain structural features that are, to the best of our knowledge, unprecedented among natural products. Applications across diverse marine habitats reveal biome-specific metabolomic signatures and levels of chemical diversity in concordance with sequence-based predictions. Expanded deployments, in situ cultivation, and metagenomics facilitate compound discovery, enhance yields, and link compounds to candidate producing organisms, although microbial community complexity creates challenges for the later. This compound-first approach to natural product discovery provides access to poorly explored chemical space and has implications for drug discovery and the detection of chemically mediated biotic interactions. Environmental analyses predict extensive, yet to be realized natural product diversity. Herein, the authors report an approach that directly captures natural products from the environment, circumventing previous challenges and yielding compounds with unusual structures and activities.
引用
收藏
页数:14
相关论文
共 90 条
  • [1] Microbial genome mining for accelerated natural products discovery: is a renaissance in the making?
    Bachmann, Brian O.
    Van Lanen, Steven G.
    Baltz, Richard H.
    [J]. JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY, 2014, 41 (02) : 175 - 184
  • [2] Marcel Faber Roundtable: Is our antibiotic pipeline unproductive because of starvation, constipation or lack of inspiration?
    Baltz, Richard H.
    [J]. JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY, 2006, 33 (07) : 507 - 513
  • [3] Complete genome sequence of the model actinomycete Streptomyces coelicolor A3(2)
    Bentley, SD
    Chater, KF
    Cerdeño-Tárraga, AM
    Challis, GL
    Thomson, NR
    James, KD
    Harris, DE
    Quail, MA
    Kieser, H
    Harper, D
    Bateman, A
    Brown, S
    Chandra, G
    Chen, CW
    Collins, M
    Cronin, A
    Fraser, A
    Goble, A
    Hidalgo, J
    Hornsby, T
    Howarth, S
    Huang, CH
    Kieser, T
    Larke, L
    Murphy, L
    Oliver, K
    O'Neil, S
    Rabbinowitsch, E
    Rajandream, MA
    Rutherford, K
    Rutter, S
    Seeger, K
    Saunders, D
    Sharp, S
    Squares, R
    Squares, S
    Taylor, K
    Warren, T
    Wietzorrek, A
    Woodward, J
    Barrell, BG
    Parkhill, J
    Hopwood, DA
    [J]. NATURE, 2002, 417 (6885) : 141 - 147
  • [4] Bioactive microbial metabolites -: A personal view
    Bérdy, J
    [J]. JOURNAL OF ANTIBIOTICS, 2005, 58 (01) : 1 - 26
  • [5] Acyldepsipeptide HDAC Inhibitor Production Induced in Burkholderia thailandensis
    Biggins, John B.
    Gleber, Conrad D.
    Brady, Sean F.
    [J]. ORGANIC LETTERS, 2011, 13 (06) : 1536 - 1539
  • [6] antiSMASH 5.0: updates to the secondary metabolite genome mining pipeline
    Blin, Kai
    Shaw, Simon
    Steinke, Katharina
    Villebro, Rasmus
    Ziemert, Nadine
    Lee, Sang Yup
    Medema, Marnix H.
    Weber, Tilmann
    [J]. NUCLEIC ACIDS RESEARCH, 2019, 47 (W1) : W81 - W87
  • [7] Cell Painting, a high-content image-based assay for morphological profiling using multiplexed fluorescent dyes
    Bray, Mark-Anthony
    Singh, Shantanu
    Han, Han
    Davis, Chadwick T.
    Borgeson, Blake
    Hartland, Cathy
    Kost-Alimova, Maria
    Gustafsdottir, Sigrun M.
    Gibson, Christopher C.
    Carpenter, Anne E.
    [J]. NATURE PROTOCOLS, 2016, 11 (09) : 1757 - 1774
  • [8] Wnt Activation and Reduced Cell-Cell Contact Synergistically Induce Massive Expansion of Functional Human iPSC-Derived Cardiomyocytes
    Buikema, Jan W.
    Lee, Soah
    Goodyer, William R.
    Maas, Renee G.
    Chirikian, Orlando
    Li, Guang
    Miao, Yi
    Paige, Sharon L.
    Lee, Daniel
    Wu, Haodi
    Paik, David T.
    Rhee, Siyeon
    Tian, Lei
    Galdos, Francisco X.
    Puluca, Nazan
    Beyersdorf, Benjamin
    Hu, James
    Beck, Aimee
    Venkamatran, Sneha
    Swami, Srilatha
    Wijnker, Paul
    Schuldt, Maike
    Dorsch, Larissa M.
    van Mil, Alain
    Red-Horse, Kristy
    Wu, Joy Y.
    Geisen, Caroline
    Hesse, Michael
    Serpooshan, Vahid
    Jovinge, Stefan
    Fleischmann, Bernd K.
    Doevendans, Pieter A.
    van der Velden, Jolanda
    Garcia, K. Christopher
    Wu, Joseph C.
    Sluijter, Joost P. G.
    Wu, Sean M.
    [J]. CELL STEM CELL, 2020, 27 (01) : 50 - +
  • [9] Mining microbial genomes for new natural products and biosynthetic pathways
    Challis, Gregory L.
    [J]. MICROBIOLOGY-SGM, 2008, 154 : 1555 - 1569
  • [10] Biogeographic patterns of biosynthetic potential and specialized metabolites in marine sediments
    Chase, Alexander B.
    Bogdanov, Alexander
    Demko, Alyssa M.
    Jensen, Paul R.
    [J]. ISME JOURNAL, 2023, 17 (07) : 976 - 983