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Patellamide A and C biosynthesis by a microcin-like pathway in Prochloron didemni , the cyanobacterial symbiont of Lissoclinum patella
Open accessAbstract
Prochloron spp. are obligate cyanobacterial symbionts of many didemnid family ascidians. It has been proposed that the cyclic peptides of the patellamide class found in didemnid extracts are synthesized by Prochloron spp., but studies in which host and symbiont cells are separated and chemically analyzed to identify the biosynthetic source have yielded inconclusive results. As part of the Prochloron didemni sequencing project, we identified patellamide biosynthetic genes and confirmed their function by heterologous expression of the whole pathway in Escherichia coli . The primary sequence of patellamides A and C is encoded on a single ORF that resembles a precursor peptide. We propose that this prepatellamide is heterocyclized to form thiazole and oxazoline rings, and the peptide is cleaved to yield the two cyclic patellamides, A and C. This work represents the full sequencing and functional expression of a marine natural-product pathway from an obligate symbiont. In addition, a related cluster was identified in Trichodesmium erythraeum IMS101, an important bloom-forming cyanobacterium.
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Citations
Cites
The Pfam Protein Families Database
Bateman, A. G. (2002) · Nucleic Acids Research · doi:10.1093/nar/30.1.276 · Cited by 14,075
Improved microbial gene identification with GLIMMER
Delcher, A. L. (1999) · Nucleic Acids Research · doi:10.1093/nar/27.23.4636 · Cited by 2,493
Besemer, J., Lomsadze, A., & Borodovsky, M. (2001) · Nucleic Acids Research · doi:10.1093/nar/29.12.2607 · Cited by 2,343
Complete Genome Sequence of a Virulent Isolate of Streptococcus pneumoniae
Tettelin, H., Nelson, K. E., Paulsen, I. T., Eisen, J. A., Read, T. D., Peterson, S. N., Heidelberg, J. F., DeBoy, R. T., Haft, D. H., Dodson, R. J., et al. (2001) · Science · doi:10.1126/science.1061217 · Cited by 1,341
Self-citationThe Pfam Protein Families Database
Bateman, A. G., Birney, E., Cerruti, L., Durbin, R. M., Etwiller, L., Eddy, S. R., Griffiths‐Jones, S., Howe, K., Marshall, M. S., & Sonnhammer, E. L. L. (2002) · PubMed Central · Cited by 764
Marine Natural Products and Related Compounds in Clinical and Advanced Preclinical Trials
Newman, D. J., & Cragg, G. M. L. (2004) · Journal of Natural Products · doi:10.1021/np040031y · Cited by 758
Biosynthesis and Mode of Action of Lantibiotics
Chatterjee, C., Paul, M., Xie, L., & van der Donk, W. A. (2005) · Chemical Reviews · doi:10.1021/cr030105v · Cited by 740
Marine natural products as anticancer drugs
Simmons, T. L., Andrianasolo, E., McPhail, K., Flatt, P., & Gerwick, W. H. (2005) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.333.4.2 · Cited by 597
Piel, J., Hui, D., Wen, G., Butzke, D., Platzer, M., Fusetani, N., & Matsunaga, S. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0405976101 · Cited by 543
Prepeptide sequence of epidermin, a ribosomally synthesized antibiotic with four sulphide-rings
Schnell, N. F., Entian, K., Schneider, U., Götz, F., Zähner, H., Kellner, R., & Jung, G. (1988) · Nature · doi:10.1038/333276a0 · Cited by 538
Flagged first, then by citations
Research works printed but not linked: 5
- Faulkner, D. J., He, H. Y., Unson, M. D. & Bewley, C. A. (1993) Gazz. Chim. Ital. 123, 301-307.
- Sings, H. L. & Rinehart, K. L. (1996) J. Ind. Microbiol. 17, 385-396.
- Haygood, M. G., Schmidt, E. W., Davidson, S. K. & Faulkner, D. J. (1999) J. Mol. Microbiol. Biotechnol. 1, 33-34.10941782
- Kline, T. C. & Lewin, R. A. (1999) Symbiosis 26, 193-198.
- Swift, H. & Robertson, D. L. (1991) Symbiosis 10, 95-113.
Cited by
Sorted by citations
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Self-citationA new family of ATP-dependent oligomerization-macrocyclization biocatalysts
Kadi, N., Oves‐Costales, D., Barona‐Gómez, F., & Challis, G. L. (2007) · Nature Chemical Biology · doi:10.1038/nchembio.2007.23 · Cited by 123
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Yang, X., & van der Donk, W. A. (2013) · Chemistry - A European Journal · doi:10.1002/chem.201300401 · Cited by 125
Jones, A. C., Monroe, E. A., Eisman, E. B., Gerwick, L. G., Sherman, D. H., & Gerwick, W. H. (2010) · Natural Product Reports · doi:10.1039/c000535e · Cited by 121
Ziemert, N., Ishida, K., Quillardet, P., Bouchier, C., Hertweck, C., de Marsac, N. T., & Dittmann, E. (2008) · Applied and Environmental Microbiology · doi:10.1128/aem.02392-07 · Cited by 121
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Jakubowska, N., & Szeląg‐Wasielewska, E. (2015) · Marine Drugs · doi:10.3390/md13031497 · Cited by 119
Piel, J. (2010) · Annual Review of Microbiology · doi:10.1146/annurev-micro-090110-102805 · Cited by 120
Kennedy, J., Marchesi, J. R., & Dobson, A. D. W. (2007) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-007-0875-2 · Cited by 123
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Ishida, K., Welker, M., Christiansen, G., Cadel-Six, S., Bouchier, C., Dittmann, E., Hertweck, C., & de Marsac, N. T. (2009) · Applied and Environmental Microbiology · doi:10.1128/aem.02258-08 · Cited by 119
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An Overview on Marine Sponge-Symbiotic Bacteria as Unexhausted Sources for Natural Product Discovery
Brinkmann, C., Marker, A., & Kurtböke, D. İ. (2017) · Diversity · doi:10.3390/d9040040 · Cited by 121
The Natural Products Chemistry of Cyanobacteria
Tidgewell, K. J., Clark, B. R., & Gerwick, W. H. (2010) · Elsevier eBooks · doi:10.1016/b978-008045382-8.00041-1 · Cited by 117
Rounge, T. B., Rohrlack, T., Nederbragt, A. J., Kristensen, T., & Jakobsen, K. S. (2009) · BMC Genomics · doi:10.1186/1471-2164-10-396 · Cited by 115
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Goto, Y., Ito, Y., Kato, Y., Tsunoda, S., & Suga, H. (2014) · Chemistry & Biology · doi:10.1016/j.chembiol.2014.04.008 · Cited by 110
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Schmidt, E. W. (2008) · Nature Chemical Biology · doi:10.1038/nchembio.101 · Cited by 101
Self-citationBarber, C. J. S., Pujara, P. T., Reed, D. W., Chiwocha, S., Zhang, H., & Covello, P. S. (2013) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.437947 · Cited by 99
Accessing chemical diversity from the uncultivated symbionts of small marine animals
Smith, T. E., Pond, C. D., Pierce, E., Harmer, Z. P., Kwan, J. C., Zachariah, M. M., Harper, M. K., Wyche, T. P., Matainaho, T. K., Bugni, T. S., et al. (2018) · Nature Chemical Biology · doi:10.1038/nchembio.2537 · Cited by 97
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Giordano, D., Costantini, M., Coppola, D., Lauritano, C., Núñez‐Pons, L., Ruocco, N., di Prisco, G., Ianora, A., & Verde, C. (2018) · Advances in microbial physiology/Advances in Microbial Physiology · doi:10.1016/bs.ampbs.2018.05.002 · Cited by 92
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Müller, D., Krick, A., Kehraus, S., Mehner, C., Hart, M. C., Küpper, F. C., Saxena, K., Prinz, H., Schwalbe, H., Janning, P., et al. (2006) · Journal of Medicinal Chemistry · doi:10.1021/jm060327w · Cited by 92
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Ozaki, T., Yamashita, K., Goto, Y., Shimomura, M., Hayashi, S., Asamizu, S., Sugai, Y., Ikeda, H., Suga, H., & Onaka, H. (2017) · Nature Communications · doi:10.1038/ncomms14207 · Cited by 87
Ongley, S. E., Bian, X., Zhang, Y., Chau, R., Gerwick, W. H., Müller, R., & Neilan, B. A. (2013) · ACS Chemical Biology · doi:10.1021/cb400189j · Cited by 86
Mutalipassi, M., Riccio, G., Mazzella, V., Galasso, C., Somma, E., Chiarore, A., de Pascale, D., & Zupo, V. (2021) · Marine Drugs · doi:10.3390/md19040227 · Cited by 97
Wenski, S. L., Thiengmag, S., & Helfrich, E. J. N. (2022) · Synthetic and Systems Biotechnology · doi:10.1016/j.synbio.2022.01.007 · Cited by 86
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Leal, M. C., Sheridan, C., Osinga, R., Dionísio, G., Rocha, R. J. M., Silva, B. B. F. F. D., Rosa, R., & Calado, R. (2014) · Marine Drugs · doi:10.3390/md12073929 · Cited by 92
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Metadata
- Authors
- Schmidt, E. W., Nelson, J. T., Rasko, D. A., Sudek, S., Eisen, J. A., Haygood, M. G., & Ravel, J.
- Affiliations
- Scripps Institution of Oceanography (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2005-05-09
- Volume
- 102
- Issue
- 20
- Pages
- 7315-7320
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC1091749
- OpenAlex
- W2162481919
- Cited by
- 567
- References
- 53
- Citations by year
- 2026: 12 · 2025: 14 · 2024: 14 · 2023: 12 · 2022: 27 · 2021: 22 · 2020: 22 · 2019: 28 · 2018: 26 · 2017: 33 · 2016: 26 · 2015: 27 · 2014: 38 · 2013: 32 · 2012: 41
- FWCI
- 18.29
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- other-oa
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion, other-oa)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion, other-oa)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- National Science Foundation (0412226)
- Topics
- Life Sciences › Immunology and Microbiology › Applied Microbiology and Biotechnology › Microbial Natural Products and Biosynthesis
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biotechnology › Marine Sponges and Natural Products
- Physical Sciences › Chemistry › Organic Chemistry › Isoquinoline Alkaloid Synthesis
- Keywords
- cyanobacterial symbionts, Lissoclinum patella, heterocyclization, biosynthetic gene clusters, Trichodesmium erythraeum, marine natural products, heterologous expression
- MeSH terms
- Cyanobacteria, Amino Acid Sequence, Animals, Bacteriocins, Chromatography, High Pressure Liquid, Escherichia coli, Molecular Sequence Data, Peptides, Cyclic, Symbiosis, Urochordata, Open Reading Frames, Sequence Analysis, DNA, DNA Primers, Palau, Prochloron
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