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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
Items 401–500 of 569
Joseph, A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-809357-3.00009-6 · Cited by 13
Fukuhara, K., Takada, K., Watanabe, R., Suzuki, T., Okada, S., & Matsunaga, S. (2018) · Journal of Natural Products · doi:10.1021/acs.jnatprod.8b00591 · Cited by 13
Martínez‐García, M., Díaz‐Valdés, M., & Antón, J. (2009) · FEMS Microbiology Ecology · doi:10.1111/j.1574-6941.2009.00816.x · Cited by 12
Peach, K. C., & Linington, R. G. (2009) · Future Medicinal Chemistry · doi:10.4155/fmc.09.56 · Cited by 12
Density functional theory studies of oxygen and carbonate binding to a dicopper patellamide complex
Latifi, R., Bagherzadeh, M., Milne, B. F., Jaspars, M., & de Visser, S. P. (2008) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2008.08.009 · Cited by 12
Extending the Biosynthetic Repertoire in Ribosomal Peptide Assembly
Moore, B. S. (2008) · Angewandte Chemie International Edition · doi:10.1002/anie.200803868 · Cited by 12
Structure, function, and biosynthesis of thiazole/oxazole-modified microcins
Metelev, M., & Ghilarov, D. (2014) · Molecular Biology · doi:10.1134/s0026893314010105 · Cited by 12
Stopping Trouble before It Starts
Clardy, J. (2006) · ACS Chemical Biology · doi:10.1021/cb0600029 · Cited by 12
Kwan, J. C. (2018) · mSystems · doi:10.1128/msystems.00186-17 · Cited by 11
A New Cyclase Family Catalyzing Head-to-Tail Macrolactamization of Non-ribosomal Peptides
Matsuda, K., Kuranaga, T., & Wakimoto, T. (2019) · Journal of Synthetic Organic Chemistry Japan · doi:10.5059/yukigoseikyokaishi.77.1106 · Cited by 11
Secondary Metabolism in Myxobacteria
Bode, H. B., & Müller, R. (2014) · ASM Press eBooks · doi:10.1128/9781555815677.ch15 · Cited by 11
Behrendt, L., Raina, J., Lutz, A., Kot, W., Albertsen, M., Nielsen, P. H., Sørensen, S. J., Larkum, A. W. D., & Kühl, M. (2017) · The ISME Journal · doi:10.1038/ismej.2017.192 · Cited by 10
Chemical War in Marine Animal Forests: Natural Products and Chemical Interactions
Àvila, C. (2020) · Springer eBooks · doi:10.1007/978-3-030-57054-5_9 · Cited by 10
Shao, J. (2008) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.0804.282 · Cited by 10
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Ogawara, H. (2018) · Molecules · doi:10.3390/molecules23061476 · Cited by 11
Biosynthetic potential of culturable bacteria associated with Apostichopus japonicus
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Walsh, C. T. (2017) · Natural Product Reports · doi:10.1039/c7np00011a · Cited by 9
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Rumengan, I. F. M., Roring, V. I. Y., Haedar, J. R., Siby, M. S., Luntungan, A. H., Kolondam, B. J., Uria, A. R., & Wakimoto, T. (2021) · Symbiosis · doi:10.1007/s13199-021-00766-4 · Cited by 9
Wells, K. N., Videau, P., Nelson, D., Eiting, J., & Philmus, B. J. (2018) · FEMS Microbiology Letters · doi:10.1093/femsle/fny164 · Cited by 8
Secondary Metabolites from the Marine Tunicate “Phallusia nigra” and Some Biological Activities
Asayesh, G., Mohebbi, G., Nabipour, I., Rezaei, A., & Vazirizadeh, A. (2021) · Biology Bulletin · doi:10.1134/s1062359021030031 · Cited by 8
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Challis, G. L. (2006) · Nature Chemical Biology · doi:10.1038/nchembio0806-398 · Cited by 8
The ascidian Lissoclinum patella, the patellamides and copper
Baur, P., Comba, P., Gahan, L. R., & Scholz, C. (2022) · Australian Journal of Chemistry · doi:10.1071/ch22200 · Cited by 8
Comba, P., & Eisenschmidt, A. (2017) · Biological magnetic resonance · doi:10.1007/978-3-319-59100-1_2 · Cited by 7
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Emerging Trends for Stimulating the Discovery of Natural Products
Adnani, N., Ellis, G. A., Wyche, T. P., Bugni, T. S., Kwan, J. C., & Schmidt, E. W. (2014) · Natural Products Analysis · doi:10.1002/9781118876015.ch5 · Cited by 7
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Antholine, W. E., Bennett, B., & Hanson, G. R. (2011) · doi:10.1002/9783527633531.ch16 · Cited by 7
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Sierra, S., Dalmau, D., Higuera, S., Cortés, D., Crespo, O., Jiménez, A. I., Pop, A., Silvestru, C., & Urriolabeitia, E. P. (2021) · The Journal of Organic Chemistry · doi:10.1021/acs.joc.1c01458 · Cited by 6
Amedei, A., & Niccolai, E. (2014) · Natural Products Analysis · doi:10.1002/9781118876015.ch4 · Cited by 7
Crüsemann, M., Reher, R., Schamari, I., Brachmann, A. O., Ohbayashi, T., Kuschak, M., Malfacini, D., Seidinger, A., Pinto‐Carbó, M., Richarz, R., et al. (2017) · Angewandte Chemie · doi:10.1002/ange.201707996 · Cited by 5
Symbiont frequency predicts microbiome composition in a model bryozoan-bacterial symbiosis
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Ramm, S., Krawczyk, B., Mühlenweg, A., Poch, A., Mösker, E., & Süßmuth, R. D. (2017) · Angewandte Chemie · doi:10.1002/ange.201703488 · Cited by 5
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Kazmi, M. T., Amir, M., Iqbal, M. A., Rashid, M., & Husain, A. (2023) · Chemistry & Biodiversity · doi:10.1002/cbdv.202301662 · Cited by 4
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Chen, L., Liu, C., Liu, X., & Wang, G. (2020) · Journal of Applied Microbiology · doi:10.1111/jam.14667 · Cited by 4
Cryptic genetic lineages of a colonial ascidian host distinct microbiomes
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Purushothaman, M., Sarkar, S., Morita, M., Gugger, M. F., Schmidt, E. W., & Morinaka, B. I. (2021) · Angewandte Chemie · doi:10.1002/ange.202015975 · Cited by 4
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Kelly, W. L. (2012) · Nature Chemical Biology · doi:10.1038/nchembio.973 · Cited by 4
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Namikoshi, M., & Xu, J. (2009) · Science Publishers eBooks · doi:10.1201/b10191-5 · Cited by 4
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Okino, T. (2006) · Springer eBooks · doi:10.1007/7081_044 · Cited by 4
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Tian, X., Lyu, C., Zhou, Y., Zhang, L., Fan, A., & Liu, Z. (2026) · Marine Drugs · doi:10.3390/md24010020 · Cited by 4
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Menabit, S., Lavin, P. L., Begun, T., Mureșan, M., Teacă, A., & Purcărea, C. (2024) · Frontiers in Marine Science · doi:10.3389/fmars.2023.1279849 · Cited by 3
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Lauer, A. (2016) · Advances in environmental microbiology · doi:10.1007/978-3-319-28068-4_9 · Cited by 3
Tang, K. C., & Raj, M. (2020) · Angewandte Chemie · doi:10.1002/ange.202007608 · Cited by 3
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Muthan, K., Venkatesh, S., Asha, S., Rathika, R. K., Poomani, M. S., Mariappan, I., & Shiny, M. A. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-91631-8.00004-4 · Cited by 2
Betcher, M. A. (2011) · doi:10.6083/m4vd6wfk · Cited by 2
Zarins-Tutt, J. S., Abraham, E. R., Bailey, C. S., & Goss, R. J. M. (2017) · Progress in molecular and subcellular biology · doi:10.1007/978-3-319-51284-6_5 · Cited by 2
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Leikoski, N. (2013) · Työväentutkimus Vuosikirja · Cited by 2
Silva, C. S. P. (2006) · doi:10.11606/d.64.2006.tde-12072006-095306 · Cited by 2
Kornprobst, J. (2014) · Wiley eBooks · doi:10.1002/9783527335855.marprod028 · Cited by 2
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Webb, E. A., Foster, R. A., Villareal, T. A., Waterbury, J. B., & Zehr, J. P. (2022) · Bergey's Manual of Systematics of Archaea and Bacteria · doi:10.1002/9781118960608.gbm00448.pub2 · Cited by 2
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Li, F., Zhou, C., Wang, Y., Mengmeng, Y. U., & Ju, J. (2025) · Natural Product Reports · doi:10.1039/d5np00056d · Cited by 1
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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
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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