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REVIEW (Open Access)

Ribosomally synthesised and post-translationally modified peptides (RiPPs) from marine demosponges and their microsymbionts

Lakmini Kosgahakumbura A B # , Jayani Gamage https://orcid.org/0000-0001-9497-986X A B # , Chamari M. Hettiarachchi B , Paco Cárdenas A C and Sunithi Gunasekera https://orcid.org/0000-0002-1089-4015 A *
+ Author Affiliations
- Author Affiliations

A Pharmacognosy, Department of Pharmaceutical Biosciences, BMC, Uppsala University, Box 591, SE-75124 Uppsala, Sweden.

B Department of Chemistry, University of Colombo, Colombo, 03, Sri Lanka.

C Museum of Evolution, Uppsala University, Uppsala, Sweden.




Lakmini Kosgahakumbura completed her PhD at the University of Colombo, Sri Lanka, in collaboration with Uppsala University, Sweden. Her doctoral research focused on integrative taxonomy and isolation of bioactive natural products from marine sponges. Her particular interests are the isolation, characterisation, and evaluation of the biological significance of bromopyrrole alkaloids and Ribosomally synthesised and post-translationally modified peptides (RiPPs). The potential bioactivities of these compounds serve as valuable leads for future drug discovery.



Jayani Gamage completed her PhD at the University of Colombo, Sri Lanka, in collaboration with Uppsala University, Sweden. Her doctoral research focused on the integrative taxonomy and antimicrobial potential of shallow-water marine sponges, along with the phylogenetic relationships of selected species. This research contributed to documenting understudied marine biodiversity in the region and highlighted the bioactive potential of sponges as a source of natural products. She has a strong interest in combining conventional taxonomy with modern molecular and chemical approaches to better understand sponge diversity and bioactive potential.



Chamari Hettiarachchi is a professor in molecular biology and biochemistry at the Department of Chemistry, University of Colombo, Sri Lanka. Her research interests span molecular biology, biochemistry and microbiology, with a strong focus on cellular and molecular mechanisms and their applications in biotechnology. She has published over 50 peer-reviewed articles and has actively engaged in collaborative research with institutes in Sweden and India. Her ongoing work emphasises integrating fundamental molecular insights with applied research to address contemporary challenges in medicine, industry and the environment.



Paco Cárdenas is a sponge biologist and head curator of zoology at the Museum of Evolution, Uppsala University, Sweden. He obtained his PhD at the University of Bergen, Norway, on the systematics of tetractinellid sponges. His expertise today centres on the evolution, taxonomy and classification of demosponges, using different sets of characters including genetics and chemistry. He has described more than 30 new species of sponges worldwide. Paco also contributes to sponge pharmacognosy and metabolomics research in the Pharmacognosy group at Uppsala University.



Sunithi Gunasekera is a adjunct lecturer and associate professor in the Pharmacognosy group, Department of Pharmaceutical Biosciences, Uppsala University, Sweden. She obtained her PhD in Structural Biology in 2009 from The University of Queensland, Australia. During her doctoral research, Sunithi worked on early cyclotide bioactivity grafting applications, which sparked her interest in peptide therapeutic development. Sunithi’s research expertise spans peptide synthesis and NMR-based structural analysis. Currently, Sunithi is engaged in ribosomal peptide discovery from marine sponges from underexplored marine environments across the tropics and the North Atlantic.

* Correspondence to: sunithi.gunasekera@uu.se

# These authors equally contributed to this work.

Handling Editor: Mibel Aguilar

Australian Journal of Chemistry 78, CH25100 https://doi.org/10.1071/CH25100
Submitted: 23 June 2025  Accepted: 2 September 2025  Published online: 8 October 2025

© 2025 The Author(s) (or their employer(s)). Published by CSIRO Publishing. This is an open access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND)

Abstract

Marine sponges are among the oldest animals to have emerged on Earth. They are metazoan holobionts that host diverse microbial symbionts, which constitute more than 40% of their biomass. Despite their morphological simplicity, sponges exhibit complex genetic architecture, unquestionably encoding ribosomally synthesised and post-translationally modified peptides (RiPPs) and proteins, essential for their biological functions. In addition to host-derived compounds, the associated microbiota also produce RiPPs, introducing further complexity in distinguishing the origin of these molecules. To date, marine sponge RiPPs research is confined to species within the class Demospongiae, with peptidomic, transcriptomic and genomic approaches employed for their discovery. This review provides a comprehensive account of current research on ribosomal peptides in marine sponges and associated microsymbionts, emphasising the need for expanded discovery efforts. Unravelling the genetic basis and biosynthetic pathways of these peptides will deepen our understanding of sponge biology and open new opportunities for peptide-based drug discovery.

Keywords: demosponges, marine, microsymbionts, metagenomics, peptides, peptidomics, post-translational modifications, RiPPs, sponges, transcriptomics.

Biographies

CH25100_B1.gif

Lakmini Kosgahakumbura completed her PhD at the University of Colombo, Sri Lanka, in collaboration with Uppsala University, Sweden. Her doctoral research focused on integrative taxonomy and isolation of bioactive natural products from marine sponges. Her particular interests are the isolation, characterisation, and evaluation of the biological significance of bromopyrrole alkaloids and Ribosomally synthesised and post-translationally modified peptides (RiPPs). The potential bioactivities of these compounds serve as valuable leads for future drug discovery.

CH25100_B2.gif

Jayani Gamage completed her PhD at the University of Colombo, Sri Lanka, in collaboration with Uppsala University, Sweden. Her doctoral research focused on the integrative taxonomy and antimicrobial potential of shallow-water marine sponges, along with the phylogenetic relationships of selected species. This research contributed to documenting understudied marine biodiversity in the region and highlighted the bioactive potential of sponges as a source of natural products. She has a strong interest in combining conventional taxonomy with modern molecular and chemical approaches to better understand sponge diversity and bioactive potential.

CH25100_B3.gif

Chamari Hettiarachchi is a professor in molecular biology and biochemistry at the Department of Chemistry, University of Colombo, Sri Lanka. Her research interests span molecular biology, biochemistry and microbiology, with a strong focus on cellular and molecular mechanisms and their applications in biotechnology. She has published over 50 peer-reviewed articles and has actively engaged in collaborative research with institutes in Sweden and India. Her ongoing work emphasises integrating fundamental molecular insights with applied research to address contemporary challenges in medicine, industry and the environment.

CH25100_B4.gif

Paco Cárdenas is a sponge biologist and head curator of zoology at the Museum of Evolution, Uppsala University, Sweden. He obtained his PhD at the University of Bergen, Norway, on the systematics of tetractinellid sponges. His expertise today centres on the evolution, taxonomy and classification of demosponges, using different sets of characters including genetics and chemistry. He has described more than 30 new species of sponges worldwide. Paco also contributes to sponge pharmacognosy and metabolomics research in the Pharmacognosy group at Uppsala University.

CH25100_B5.gif

Sunithi Gunasekera is a adjunct lecturer and associate professor in the Pharmacognosy group, Department of Pharmaceutical Biosciences, Uppsala University, Sweden. She obtained her PhD in Structural Biology in 2009 from The University of Queensland, Australia. During her doctoral research, Sunithi worked on early cyclotide bioactivity grafting applications, which sparked her interest in peptide therapeutic development. Sunithi’s research expertise spans peptide synthesis and NMR-based structural analysis. Currently, Sunithi is engaged in ribosomal peptide discovery from marine sponges from underexplored marine environments across the tropics and the North Atlantic.

References

Feuda R, Dohrmann M, Pett W, Philippe H, Rota-Stabelli O, Lartillot N, et al. Improved modeling of compositional heterogeneity supports sponges as sister to all other animals. Curr Biol 2017; 27: 3864-3870.
| Crossref | Google Scholar | PubMed |

Nielsen C. Early animal evolution: a morphologist’s view. R Soc Open Sci 2019; 6: 190638.
| Crossref | Google Scholar | PubMed |

Simion P, Philippe H, Baurain D, Jager M, Richter DJ, Di Franco A, et al. A large and consistent phylogenomic dataset supports sponges as the sister group to all other animals. Curr Biol 2017; 27: 958-967.
| Crossref | Google Scholar | PubMed |

de Voogd N, Alvarez B, Boury-Esnault N, Cárdenas P, Díaz M, Dohrmann M, et al. The World Porifera database. 2025. Available at https://www.marinespecies.org/porifera/index.php

Van Soest RW, Boury-Esnault N, Vacelet J, Dohrmann M, Erpenbeck D, De Voogd NJ, et al. Global diversity of sponges (Porifera). PLoS ONE 2012; 7: e35105.
| Crossref | Google Scholar | PubMed |

Webster NS, Taylor MW. Marine sponges and their microbial symbionts: love and other relationships. Environ Microbiol 2012; 14: 335-346.
| Crossref | Google Scholar | PubMed |

Pita L, Rix L, Slaby BM, Franke A, Hentschel U. The sponge holobiont in a changing ocean: from microbes to ecosystems. Microbiome 2018; 6: 46.
| Crossref | Google Scholar | PubMed |

Bourguet‐Kondracki ML, Kornprobst JM. Promising marine molecules in pharmacology. In: La Barre S, Kornprobst J-M, editors. Outstanding Marine Molecules. Wiley; 2014. pp. 243–264.

Cheng M-M, Tang X-L, Sun Y-T, Song D-Y, Cheng Y-J, Liu H, et al. Biological and chemical diversity of marine sponge-derived microorganisms over the last two decades from 1998 to 2017. Molecules 2020; 25: 853.
| Crossref | Google Scholar | PubMed |

10  Han B-N, Hong L-L, Gu B-B, Sun Y-T, Wang J, Liu J-T, et al. Natural products from sponges. In: Li Z, editor. Symbiotic Microbiomes of Coral Reefs Sponges and Corals. Springer; 2019. pp. 329–463.

11  Hong L-L, Ding Y-F, Zhang W, Lin H-W. Chemical and biological diversity of new natural products from marine sponges: a review (2009–2018). Mar Life Sci Tech 2022; 4: 356-372.
| Crossref | Google Scholar | PubMed |

12  Nadar VM, Manivannan S, Chinnaiyan R, Govarthanan M, Ponnuchamy K. Review on marine sponge alkaloid, aaptamine: a potential antibacterial and anticancer drug. Chem Biol Drug Des 2022; 99: 103-110.
| Crossref | Google Scholar | PubMed |

13  Pokharkar O, Lakshmanan H, Zyryanov G, Tsurkan M. In silico evaluation of antifungal compounds from marine sponges against COVID-19-associated mucormycosis. Mar Drugs 2022; 20: 215.
| Crossref | Google Scholar | PubMed |

14  Varijakzhan D, Loh J-Y, Yap W-S, Yusoff K, Seboussi R, Lim S-HE, et al. Bioactive compounds from marine sponges: Fundamentals and applications. Mar Drugs 2021; 19: 246.
| Crossref | Google Scholar | PubMed |

15  Vitali A. Antimicrobial peptides derived from marine sponges. Am J Clin Microbiol Antimicrob 2018; 1: 1006.
| Google Scholar |

16  Ruocco N, Costantini S, Palumbo F, Costantini M. Marine sponges and bacteria as challenging sources of enzyme inhibitors for pharmacological applications. Mar Drugs 2017; 15: 173.
| Crossref | Google Scholar | PubMed |

17  Sánchez-Lozano I, Hernández-Guerrero CJ, Muñoz-Ochoa M, Hellio C. Biomimetic approaches for the development of new antifouling solutions: study of incorporation of macroalgae and sponge extracts for the development of new environmentally friendly coatings. Int J Mol Sci 2019; 20: 4863.
| Crossref | Google Scholar | PubMed |

18  Tian T, Takada K, Ise Y, Ohtsuka S, Okada S, Matsunaga S. Microsclerodermins N and O, cytotoxic cyclic peptides containing a p-ethoxyphenyl moiety from a deep-sea marine sponge Pachastrella sp. Tetrahedron 2020; 76: 130997.
| Crossref | Google Scholar |

19  Singh A, Thakur NL. Significance of investigating allelopathic interactions of marine organisms in the discovery and development of cytotoxic compounds. Chem Biol Interact 2016; 243: 135-147.
| Crossref | Google Scholar | PubMed |

20  Li Q, Wang X, Korzhev M, Schröder HC, Link T, Tahir MN, et al. Potential biological role of laccase from the sponge Suberites domuncula as an antibacterial defense component. Biochim Biophys Acta 2015; 1850: 118-128.
| Crossref | Google Scholar | PubMed |

21  Mayer AM, Glaser KB, Cuevas C, Jacobs RS, Kem W, Little RD, et al. The odyssey of marine pharmaceuticals: a current pipeline perspective. Trends Pharm Sci 2010; 31: 255-265.
| Crossref | Google Scholar | PubMed |

22  Agrawal S, Acharya D, Adholeya A, Barrow CJ, Deshmukh SK. Nonribosomal peptides from marine microbes and their antimicrobial and anticancer potential. Front Pharmacol 2017; 8: 828.
| Crossref | Google Scholar | PubMed |

23  Bharathi D, Lee J. Recent advances in marine-derived compounds as potent antibacterial and antifungal agents: a comprehensive review. Mar Drugs 2024; 22: 348.
| Crossref | Google Scholar | PubMed |

24  Ribeiro R, Pinto E, Fernandes C, Sousa E. Marine cyclic peptides: antimicrobial activity and synthetic strategies. Mar Drugs 2022; 20: 397.
| Crossref | Google Scholar | PubMed |

25  Kang HK, Choi M-C, Seo CH, Park Y. Therapeutic properties and biological benefits of marine-derived anticancer peptides. Int J Mol Sci 2018; 19: 919.
| Crossref | Google Scholar | PubMed |

26  Nazarian M, Hosseini SJ, Nabipour I, Mohebbi G. Marine bioactive peptides with anti-cancer potential. Iran South Med J 2015; 18: 607-629.
| Google Scholar |

27  McKenna V, Archibald JM, Beinart R, Dawson MN, Hentschel U, Keeling PJ, et al. The aquatic symbiosis genomics project: probing the evolution of symbiosis across the tree of life. Wellcome Open Res 2021; 6: 254.
| Crossref | Google Scholar | PubMed |

28  Steffen K, Proux-Wéra E, Soler L, Churcher A, Sundh J, Cárdenas P. Whole genome sequence of the deep-sea sponge Geodia barretti (Metazoa, Porifera, Demospongiae). G3 2023; 13: jkad192.
| Crossref | Google Scholar | PubMed |

29  Macedo MWFS, Cunha NB, Carneiro JA, Costa RA, Alencar SA, Cardoso MH, et al. Marine organisms as a rich source of biologically active peptides. Front Mar Sci 2021; 8: 667764.
| Crossref | Google Scholar |

30  Urda C, Perez M, Rodriguez J, Jimenez C, Cuevas C, Fernandez R. Pembamide, a N-methylated linear peptide from a sponge Cribrochalina sp. Tetrahedron Lett 2016; 57: 3239-3242.
| Crossref | Google Scholar |

31  Afifi AH, El-Desoky AH, Kato H, Mangindaan RE, de Voogd NJ, Ammar NM, et al. Carteritins A and B, cyclic heptapeptides from the marine sponge Stylissa carteri. Tetrahedron Lett 2016; 57: 1285-1288.
| Crossref | Google Scholar |

32  Tan KC, Wakimoto T, Abe I. Sulfoureido lipopeptides from the marine sponge Discodermia kiiensis. J Nat Prod 2016; 79: 2418-2422.
| Crossref | Google Scholar | PubMed |

33  Coello L, Reyes F, Martín MJ, Cuevas C, Fernández R. Isolation and structures of pipecolidepsins A and B, cytotoxic cyclic depsipeptides from the madagascan sponge Homophymia lamellosa. J Nat Prod 2014; 77: 298-303.
| Crossref | Google Scholar | PubMed |

34  Fernández R, Bayu A, Aryono Hadi T, Bueno S, Pérez M, Cuevas C, et al. Unique polyhalogenated peptides from the marine sponge Ircinia sp. Mar Drugs 2020; 18: 396.
| Crossref | Google Scholar | PubMed |

35  Molinski TF. Cyclic azole-homologated peptides from marine sponges. Org Biomol Chem 2018; 16: 21-29.
| Crossref | Google Scholar |

36  Steffen K, Laborde Q, Gunasekera S, Payne CD, Rosengren KJ, Riesgo A, et al. Barrettides: a peptide family specifically produced by the deep-sea sponge Geodia barretti. J Nat Prod 2021; 84: 3138-3146.
| Crossref | Google Scholar | PubMed |

37  Mokhlesi A, Stuhldreier F, Wex KW, Berscheid A, Hartmann R, Rehberg N, et al. Cyclic cystine-bridged peptides from the marine sponge Clathria basilana induce apoptosis in tumor cells and depolarize the bacterial cytoplasmic membrane. J Nat Prod 2017; 80: 2941-2952.
| Crossref | Google Scholar | PubMed |

38  Ko S-C, Jang J, Ye B-R, Kim M-S, Choi I-W, Park W-S, et al. Purification and molecular docking study of angiotensin I-converting enzyme (ACE) inhibitory peptides from hydrolysates of marine sponge Stylotella aurantium. Process Biochem 2017; 54: 180-187.
| Crossref | Google Scholar |

39  Kita M, Gise B, Kawamura A, Kigoshi H. Stylissatin A, a cyclic peptide that inhibits nitric oxide production from the marine sponge Stylissa massa. Tetrahedron Lett 2013; 54: 6826-6828.
| Crossref | Google Scholar |

40  Li H, Bowling JJ, Fronczek FR, Hong J, Jabba SV, Murray TF, et al. Asteropsin A: an unusual cystine-crosslinked peptide from porifera enhances neuronal Ca2+ influx. Biochim Biophys Acta 2013; 1830: 2591-2599.
| Crossref | Google Scholar | PubMed |

41  Pozzolini M, Millo E, Oliveri C, Mirata S, Salis A, Damonte G, et al. Elicited ROS scavenging activity, photoprotective, and wound-healing properties of collagen-derived peptides from the marine sponge Chondrosia reniformis. Mar Drugs 2018; 16: 465.
| Crossref | Google Scholar | PubMed |

42  Taylor MW, Radax R, Steger D, Wagner M. Sponge-associated microorganisms: evolution, ecology, and biotechnological potential. Microbiol Mol Biol Rev 2007; 71: 295-347.
| Crossref | Google Scholar | PubMed |

43  Hamada T, Matsunaga S, Yano G, Fusetani N. Polytheonamides A and B, highly cytotoxic, linear polypeptides with unprecedented structural features, from the marine sponge, Theonella swinhoei. J Am Chem Soc 2004; 127: 110-118.
| Crossref | Google Scholar |

44  Siegl A, Hentschel U. PKS and NRPS gene clusters from microbial symbiont cells of marine sponges by whole genome amplification. Environ Microbiol Rep 2010; 2: 507-513.
| Crossref | Google Scholar | PubMed |

45  Storey MA, Andreassend SK, Bracegirdle J, Brown A, Keyzers RA, Ackerley DF, et al. Metagenomic exploration of the marine sponge Mycale hentscheli uncovers multiple polyketide-producing bacterial symbionts. MBio 2020; 11: 10.1128/mbio.02997-19.
| Crossref | Google Scholar | PubMed |

46  Guerrero-Garzón JF, Zehl M, Schneider O, Rückert C, Busche T, Kalinowski J, et al. Streptomyces spp. from the marine sponge Antho dichotoma: analyses of secondary metabolite biosynthesis gene clusters and some of their products. Front Microbiol 2020; 11: 437.
| Crossref | Google Scholar | PubMed |

47  Oves-Costales D, Sánchez-Hidalgo M, Martín J, Genilloud O. Identification, cloning and heterologous expression of the gene cluster directing RES-701-3,-4 lasso peptides biosynthesis from a marine Streptomyces strain. Mar Drugs 2020; 18: 238.
| Crossref | Google Scholar | PubMed |

48  Miranda KJ, Jaber S, Atoum D, Arjunan S, Ebel R, Jaspars M, et al. Pseudomonassin, a new bioactive ribosomally synthesised and post-translationally modified peptide from Pseudomonas sp. SST3. Microorganisms 2023; 11: 2563.
| Crossref | Google Scholar | PubMed |

49  Scholz R, Molohon KJ, Nachtigall J, Vater J, Markley AL, Süssmuth RD, et al. Plantazolicin, a novel microcin B17/streptolysin S-like natural product from Bacillus amyloliquefaciens FZB42. J Bacteriol 2011; 193: 215-224.
| Crossref | Google Scholar | PubMed |

50  Yi Y, Liang L, de Jong A, Kuipers OP. A systematic comparison of natural product potential, with an emphasis on RiPPs, by mining of bacteria of three large ecosystems. Genomics 2024; 116: 110880.
| Crossref | Google Scholar | PubMed |

51  Bibi F, Faheem M, Azhar EI, Yasir M, Alvi SA, Kamal M, et al. Bacteria from marine sponges: a source of new drugs. Curr Drug Metab 2017; 18: 11-15.
| Crossref | Google Scholar | PubMed |

52  Rubin GM, Ding Y. Recent advances in the biosynthesis of RiPPs from multicore-containing precursor peptides. J Ind Microbiol Biotechnol 2020; 47: 659-674.
| Crossref | Google Scholar | PubMed |

53  Sukmarini L. Marine bacterial ribosomal peptides: recent genomics- and synthetic biology-based discoveries and biosynthetic studies. Mar Drugs 2022; 20: 544.
| Crossref | Google Scholar | PubMed |

54  Welker M, von Döhren H. Cyanobacterial peptides – nature’s own combinatorial biosynthesis. FEMS Microbiol Rev 2006; 30: 530-563.
| Crossref | Google Scholar | PubMed |

55  Fidor A, Konkel R, Mazur-Marzec H. Bioactive peptides produced by cyanobacteria of the genus Nostoc: a review. Mar Drugs 2019; 17: 561.
| Crossref | Google Scholar | PubMed |

56  Sivonen K, Leikoski N, Fewer DP, Jokela J. Cyanobactins – ribosomal cyclic peptides produced by cyanobacteria. Appl Microbiol Biotechnol 2010; 86: 1213-1225.
| Crossref | Google Scholar | PubMed |

57  Fusetani N, Sugawara T, Matsunaga S, Hirota H. Orbiculamide A: a novel cytotoxic cyclic peptide from a marine sponge Theonella sp. J Am Chem Soc 1991; 113: 7811-7812.
| Crossref | Google Scholar |

58  Araki T, Matsunaga S, Nakao Y, Furihata K, West L, Faulkner DJ, et al. Koshikamide B, a cytotoxic peptide lactone from a marine sponge Theonella sp. J Org Chem 2008; 73: 7889-7894.
| Crossref | Google Scholar | PubMed |

59  Wakimoto T, Tan KC, Tajima H, Abe I. Cytotoxic cyclic peptides from the marine sponges. In: Kim SK, editor. Handbook of Anticancer Drugs from Marine Origin. Cham, Switzerland: Springer; 2015. pp. 113–144.

60  Lin Z, Agarwal V, Cong Y, Pomponi SA, Schmidt EW. Short macrocyclic peptides in sponge genomes. Proc Natl Acad Sci 2024; 121: e2314383121.
| Crossref | Google Scholar | PubMed |

61  Arnison PG, Bibb MJ, Bierbaum G, Bowers AA, Bugni TS, Bulaj G, et al. Ribosomally synthesized and post-translationally modified peptide natural products: overview and recommendations for a universal nomenclature. Nat Prod Rep 2013; 30: 108-160.
| Crossref | Google Scholar | PubMed |

62  Dong S-H, Liu A, Mahanta N, Mitchell DA, Nair SK. Mechanistic basis for ribosomal peptide backbone modifications. ACS Cent Sci 2019; 5: 842-851.
| Crossref | Google Scholar | PubMed |

63  Kessler SC, Chooi Y-H. Out for a RiPP: challenges and advances in genome mining of ribosomal peptides from fungi. Nat Prod Rep 2022; 39: 222-230.
| Crossref | Google Scholar | PubMed |

64  McIntosh JA, Donia MS, Schmidt EW. Ribosomal peptide natural products: bridging the ribosomal and nonribosomal worlds. Nat Prod Rep 2009; 26: 537-559.
| Crossref | Google Scholar | PubMed |

65  Montalbán-López M, Scott TA, Ramesh S, Rahman IR, van Heel AJ, Viel JH, et al. New developments in RiPP discovery, enzymology and engineering. Nat Prod Rep 2021; 38: 130-239.
| Crossref | Google Scholar | PubMed |

66  Walton JD, Hallen-Adams HE, Luo H. Ribosomal biosynthesis of the cyclic peptide toxins of Amanita mushrooms. Biopolymers 2010; 94: 659-664.
| Crossref | Google Scholar | PubMed |

67  Cheng Y-Q, Yang M, Matter AM. Characterization of a gene cluster responsible for the biosynthesis of anticancer agent FK228 in Chromobacterium violaceum No. 968. Appl Environ Microbiol 2007; 73: 3460-3469.
| Crossref | Google Scholar | PubMed |

68  Doi T, Iijima Y, Shin-Ya K, Ganesan A, Takahashi T. A total synthesis of spiruchostatin A. Tetrahedron Lett 2006; 47: 1177-1180.
| Crossref | Google Scholar |

69  Takada K, Hamada T, Hirota H, Nakao Y, Matsunaga S, van Soest RW, et al. Asteropine A, a sialidase-inhibiting conotoxin-like peptide from the marine sponge Asteropus simplex. Chem Biol 2006; 13: 569-574.
| Crossref | Google Scholar | PubMed |

70  Li H, Bowling JJ, Su M, Hong J, Lee B-J, Hamann MT, et al. Asteropsins B–D, sponge-derived knottins with potential utility as a novel scaffold for oral peptide drugs. Biochim Biophys Acta 2014; 1840: 977-984.
| Crossref | Google Scholar | PubMed |

71  Li H, Su M, Hamann MT, Bowling JJ, Kim HS, Jung JH. Solution structure of a sponge-derived cystine knot peptide and its notable stability. J Nat Prod 2014; 77: 304-310.
| Crossref | Google Scholar | PubMed |

72  Su M, Li H, Wang H, Kim EL, Kim HS, Kim E-H, et al. Stable and biocompatible cystine knot peptides from the marine sponge Asteropus sp. Bioorg Med Chem 2016; 24: 2979-2987.
| Crossref | Google Scholar | PubMed |

73  Freeman MF, Gurgui C, Helf MJ, Morinaka BI, Uria AR, Oldham NJ, et al. Metagenome mining reveals polytheonamides as posttranslationally modified ribosomal peptides. Science 2012; 338: 387-390.
| Crossref | Google Scholar | PubMed |

74  Li H, Dang HT, Li J, Sim CJ, Hong J, Kim DK, et al. Pyroglutamyl dipeptides and tetrahydro-β-carboline alkaloids from a marine sponge Asteropus sp. Biochem Syst Ecol 2010; 38: 1049-1051.
| Crossref | Google Scholar |

75  Getz JA, Rice JJ, Daugherty PS. Protease-resistant peptide ligands from a knottin scaffold library. ACS Chem Biol 2011; 6: 837-844.
| Crossref | Google Scholar | PubMed |

76  Wong CT, Rowlands DK, Wong CH, Lo TW, Nguyen GK, Li HY, et al. Orally active peptidic bradykinin B1 receptor antagonists engineered from a cyclotide scaffold for inflammatory pain treatment. Angew Chem Int Ed 2012; 51: 5620-5624.
| Crossref | Google Scholar | PubMed |

77  Carstens BB, Rosengren KJ, Gunasekera S, Schempp S, Bohlin L, Dahlström M, et al. Isolation, characterization, and synthesis of the barrettides: disulfide-containing peptides from the marine sponge Geodia barretti. J Nat Prod 2015; 78: 1886-1893.
| Crossref | Google Scholar | PubMed |

78  Sarkar N. Polyadenylation of mRNA in prokaryotes. Annu Rev Biochem 1997; 66: 173-197.
| Crossref | Google Scholar | PubMed |

79  Hausner G, Hafez M, Edgell DR. Bacterial group I introns: mobile RNA catalysts. Mob DNA 2014; 5: 8.
| Crossref | Google Scholar | PubMed |

80  Willey JM, Sherwood LM, Woolverton CJ. Prescott’s Microbiology, 11th edn. New York: McGraw-Hill Education; 2020.

81  Steffen K, Indraningrat AAG, Erngren I, Haglöf J, Becking LE, Smidt H, et al. Oceanographic setting influences the prokaryotic community and metabolome in deep-sea sponges. Sci Rep 2022; 12: 3356.
| Crossref | Google Scholar | PubMed |

82  Champ MA. Economic and environmental impacts on ports and harbors from the convention to ban harmful marine anti-fouling systems. Mar Pollut Bull 2003; 46: 935-940.
| Crossref | Google Scholar | PubMed |

83  Matsunaga S, Jimbo M, Gill MB, Wyhe LL, Murata M, Nonomura K, et al. Isolation, amino acid sequence and biological activities of novel long‐chain polyamine‐associated peptide toxins from the sponge Axinyssa aculeata. ChemBioChem 2011; 12: 2191-2200.
| Crossref | Google Scholar | PubMed |

84  Irie R, Miyako K, Matsunaga S, Sakai R, Oikawa M. Structure revision of protoaculeine B, a post-translationally modified N-terminal residue in the peptide toxin aculeine B. J Nat Prod 2021; 84: 1203-1209.
| Crossref | Google Scholar | PubMed |

85  Matsunaga S, Kishi R, Otsuka K, Fujita MJ, Oikawa M, Sakai R. Protoaculeine B, a putative N-terminal residue for the novel peptide toxin aculeines. Org Lett 2014; 16: 3090-3093.
| Crossref | Google Scholar | PubMed |

86  Watari H, Kishi R, Matsunaga S, Nishikawa T, Sawada Y, Honda A, et al. Interaction of polyamine-modified marine peptide aculeine A with cell membranes: disruption or entry. Chem Lett 2023; 52: 185-189.
| Crossref | Google Scholar |

87  Fang W-Y, Dahiya R, Qin H-L, Mourya R, Maharaj S. Natural proline-rich cyclopolypeptides from marine organisms: chemistry, synthetic methodologies and biological status. Mar Drugs 2016; 14: 194.
| Crossref | Google Scholar | PubMed |

88  Mechnich O, Messier G, Kessler H, Bernd M, Kutscher B. Cyclic heptapeptides axinastatin 2, 3, and 4: conformational analysis and evaluation of the biological potential. Helv Chim Acta 1997; 80: 1338-1354.
| Crossref | Google Scholar |

89  Malešević M, Schumann M, Jahreis G, Fischer G, Lücke C. Design of cyclic peptides featuring proline predominantly in the cis conformation under physiological conditions. ChemBioChem 2012; 13: 2122-2127.
| Crossref | Google Scholar | PubMed |

90  Mitova M, Popov S, De Rosa S. Cyclic peptides from a Ruegeria strain of bacteria associated with the sponge Suberites domuncula. J Nat Prod 2004; 67: 1178-1181.
| Crossref | Google Scholar | PubMed |

91  Iwasaki K, Iwasaki A, Sumimoto S, Sano T, Hitomi Y, Ohno O, et al. Croissamide, a proline-rich cyclic peptide with an N-prenylated tryptophan from a marine cyanobacterium Symploca sp. Tetrahedron Lett 2018; 59: 3806-3809.
| Crossref | Google Scholar |

92  Montaser R, Abboud KA, Paul VJ, Luesch H. Pitiprolamide, a proline-rich dolastatin 16 analogue from the marine cyanobacterium Lyngbya majuscula from Guam. J Nat Prod 2011; 74: 109-112.
| Crossref | Google Scholar | PubMed |

93  Mistry J, Finn RD, Eddy SR, Bateman A, Punta M. Challenges in homology search: HMMER3 and convergent evolution of coiled-coil regions. Nucleic Acids Res 2013; 41: e121.
| Crossref | Google Scholar | PubMed |

94  Schmidt G, Grube A, Köck M. Stylissamides A–D – new proline‐containing cyclic heptapeptides from the marine sponge Stylissa caribica. Eur J Org Chem 2007; 24: 4103-4110.
| Crossref | Google Scholar |

95  Kobayashi Ji, Nakamura T, Tsuda M. Hymenamide F, new cyclic heptapeptide from marine sponge Hymeniacidon sp. Tetrahedron 1996; 52: 6355-6360.
| Crossref | Google Scholar |

96  Zhang H-J, Yi Y-H, Yang G-J, Hu M-Y, Cao G-D, Yang F, et al. Proline-containing cyclopeptides from the marine sponge Phakellia fusca. J Nat Prod 2010; 73: 650-655.
| Crossref | Google Scholar | PubMed |

97  Li Y, Ling H, Teruya K, Konno H. Synthesis of Stylissamide B, a pro‐rich cyclic heptapeptide isolated from the marine sponge Stylissa caribica. J Pept Sci 2025; 31: e70028.
| Crossref | Google Scholar | PubMed |

98  Krumpe LRH, Wilson BAP, Marchand C, Sunassee SN, Bermingham A, Wang W, et al. Recifin A, initial example of the tyr-lock peptide structural family, is a selective allosteric inhibitor of tyrosyl-DNA phosphodiesterase I. J Am Chem Soc 2020; 142: 21178-21188.
| Crossref | Google Scholar | PubMed |

99  Smallwood TB, Krumpe LR, Payne CD, Klein VG, O’Keefe BR, Clark RJ, et al. Picking the tyrosine-lock: chemical synthesis of the tyrosyl-DNA phosphodiesterase I inhibitor recifin A and analogues. Chem Sci 2024; 15: 13227-13233.
| Crossref | Google Scholar | PubMed |

100  Williams DE, Austin P, Diaz-Marrero AR, Soest RV, Matainaho T, Roskelley CD, et al. Neopetrosiamides, peptides from the marine sponge Neopetrosia sp. that inhibit amoeboid invasion by human tumor cells. Org Lett 2005; 7: 4173-4176.
| Crossref | Google Scholar | PubMed |

101  Liu H, Boudreau MA, Zheng J, Whittal RM, Austin P, Roskelley CD, et al. Chemical synthesis and biological activity of the Neopetrosiamides and their analogues: revision of disulfide bond connectivity. J Am Chem Soc 2010; 132: 1486-1487.
| Crossref | Google Scholar | PubMed |

102  Zhong W, Olugbami JO, Rathakrishnan P, Mohanty I, Moore SG, Garg N, et al. Discovery and folding dynamics of a fused bicyclic cysteine knot undecapeptide from the marine sponge Halichondria bowerbanki. J Org Chem 2024; 89: 12748-12752.
| Crossref | Google Scholar | PubMed |

103  Finking R, Marahiel MA. Biosynthesis of nonribosomal peptides. Annu Rev Microbiol 2004; 58: 453-488.
| Crossref | Google Scholar | PubMed |

104  Ozaki T, Minami A, Oikawa H. Recent advances in the biosynthesis of ribosomally synthesized and posttranslationally modified peptides of fungal origin. J Antibiot 2023; 76: 3-13.
| Crossref | Google Scholar | PubMed |

105  Nie Q, Sun C, Liu S, Gao X. Exploring bioactive fungal RiPPs: advances, challenges, and future prospects. Biochemistry 2024; 63: 2948-2957.
| Crossref | Google Scholar | PubMed |

106  Liang H, Song ZM, Zhong Z, Zhang D, Yang W, Zhou L, et al. Genomic and metabolic analyses reveal antagonistic lanthipeptides in Archaea. Microbiome 2023; 11: 74.
| Crossref | Google Scholar | PubMed |

107  Czekster CM, Ge Y, Naismith JH. Mechanisms of cyanobactin biosynthesis. Curr Opin Chem Biol 2016; 35: 80-88.
| Crossref | Google Scholar | PubMed |

108  Phelan RW, Barret M, Cotter PD, O’Connor PM, Chen R, Morrissey JP, et al. Subtilomycin: a new lantibiotic from Bacillus subtilis strain MMA7 isolated from the marine sponge Haliclona simulans. Mar Drugs 2013; 11: 1878-1898.
| Crossref | Google Scholar | PubMed |

109  Nagai K, Kamigiri K, Arao N, Suzumura K, Kawano Y, Yamaoka M, et al. YM-266183 and ym-266184, novel thiopeptide antibiotics produced by Bacillus cereus isolated from a marine sponge I. taxonomy, fermentation, isolation, physico-chemical properties and biological properties. J Antibiot 2003; 56: 123-128.
| Crossref | Google Scholar | PubMed |

110  Jensen MR, Freeman MF. Structure and biosynthesis of proteusin RiPP natural products. In: Liu H-W, Begley TP, editors. Comprehensive Natural Products III. Elsevier; 2020. pp. 88–118.

111  Nguyen NA, Vidya F, Yennawar NH, Wu H, McShan AC, Agarwal V. Disordered regions in proteusin peptides guide post-translational modification by a flavin-dependent RiPP brominase. Nat Commun 2024; 15: 1265.
| Crossref | Google Scholar | PubMed |

112  Bhushan A, Egli PJ, Peters EE, Freeman MF, Piel J. Genome mining- and synthetic biology-enabled production of hypermodified peptides. Nat Chem 2019; 11: 931-939.
| Crossref | Google Scholar | PubMed |

113  Bösch NM, Borsa M, Greczmiel U, Morinaka BI, Gugger M, Oxenius A, et al. Landornamides: antiviral ornithine-containing ribosomal peptides discovered through genome mining. Angew Chem Int Ed 2020; 59: 11763-11768.
| Crossref | Google Scholar | PubMed |

114  Chen N, Liu L, Wang J, Mao D, Lu H, Shishido TK, et al. Novel gene clusters for secondary metabolite synthesis in mesophotic sponge-associated bacteria. Microb Biotechnol 2025; 18: e70107.
| Crossref | Google Scholar | PubMed |

115  Freeman MF, Helf MJ, Bhushan A, Morinaka BI, Piel J. Seven enzymes create extraordinary molecular complexity in an uncultivated bacterium. Nat Chem 2017; 9: 387-395.
| Crossref | Google Scholar | PubMed |

116  Wilson MC, Mori T, Rückert C, Uria AR, Helf MJ, Takada K, et al. An environmental bacterial taxon with a large and distinct metabolic repertoire. Nature 2014; 506: 58-62.
| Crossref | Google Scholar | PubMed |

117  Iwamoto M, Shimizu H, Muramatsu I, Oiki S. A cytotoxic peptide from a marine sponge exhibits ion channel activity through vectorial-insertion into the membrane. FEBS Lett 2010; 584: 3995-3999.
| Crossref | Google Scholar | PubMed |

118  Maheshwari N, Jermiin LS, Cotroneo C, Gordon SV, Shields DC. Insights into the production and evolution of lantibiotics from a computational analysis of peptides associated with the lanthipeptide cyclase domain. R Soc Open Sci 2024; 11: 240491.
| Crossref | Google Scholar | PubMed |

119  Zhong G, Wang Z-J, Yan F, Zhang Y, Huo L. Recent advances in discovery, bioengineering, and bioactivity-evaluation of ribosomally synthesized and post-translationally modified peptides. ACS Bio Med Chem Au 2023; 3: 1-31.
| Crossref | Google Scholar | PubMed |

120  Samak ME, Solyman SM, Hanora A, Zakeer S. Metagenomic mining of two Egyptian Red Sea sponges associated microbial community. BMC Microbiol 2024; 24: 315.
| Crossref | Google Scholar | PubMed |

121  Janssen K, Krasenbrink J, Strangfeld S, Kroheck S, Josten M, Engeser M, et al. Elucidation of the bridging pattern of the lantibiotic pseudomycoicidin. ChemBioChem 2023; 24: e202200540.
| Crossref | Google Scholar | PubMed |

122  Deng Y, Li C-Z, Zhu Y-G, Wang P-X, Qi Q-D, Fu J-J, et al. ApnI, a transmembrane protein responsible for subtilomycin immunity, unveils a novel model for lantibiotic immunity. Appl Environ Microbiol 2014; 80: 6303-6315.
| Crossref | Google Scholar | PubMed |

123  Deng Y, Chen H, Li C, Xu J, Qi Q, Xu Y, et al. Endophyte Bacillus subtilis evade plant defense by producing lantibiotic subtilomycin to mask self-produced flagellin. Commun Biol 2019; 2: 368.
| Crossref | Google Scholar | PubMed |

124  Ziemert N, Alanjary M, Weber T. The evolution of genome mining in microbes – a review. Nat Prod Rep 2016; 33: 988-1005.
| Crossref | Google Scholar | PubMed |

125  McCloud TG. High throughput extraction of plant, marine and fungal specimens for preservation of biologically active molecules. Molecules 2010; 15: 4526-4563.
| Crossref | Google Scholar | PubMed |

126  Okonechnikov K, Golosova O, Fursov M, The UGENE Team. Unipro UGENE: a unified bioinformatics toolkit. Bioinformatics 2012; 28: 1166-1167.
| Crossref | Google Scholar | PubMed |

127  Teufel F, Almagro Armenteros JJ, Johansen AR, Gíslason MH, Pihl SI, Tsirigos KD, et al. SignalP 6.0 predicts all five types of signal peptides using protein language models. Nat Biotechnol 2022; 40: 1023-1025.
| Crossref | Google Scholar | PubMed |

128  Lu J, Rincon N, Wood DE, Breitwieser FP, Pockrandt C, Langmead B, et al. Metagenome analysis using the Kraken software suite. Nat Protoc 2022; 17: 2815-2839.
| Crossref | Google Scholar | PubMed |

129  Camacho C, Coulouris G, Avagyan V, Ma N, Papadopoulos J, Bealer K, et al. BLAST+: architecture and applications. BMC Bioinform 2009; 10: 421.
| Crossref | Google Scholar |

130  Jumper J, Evans R, Pritzel A, Green T, Figurnov M, Ronneberger O, et al. Highly accurate protein structure prediction with AlphaFold. Nature 2021; 596: 583-589.
| Crossref | Google Scholar | PubMed |

131  Pita L, Hoeppner MP, Ribes M, Hentschel U. Differential expression of immune receptors in two marine sponges upon exposure to microbial-associated molecular patterns. Sci Rep 2018; 8: 16081.
| Crossref | Google Scholar | PubMed |

132  Rathinam RB, Acharya A, Robina AJ, Banu H, Tripathi G. The immune system of marine invertebrates: Earliest adaptation of animals. Comp Immunol Rep 2024; 7: 200163.
| Crossref | Google Scholar |

133  Ziemert N, Jensen PR. Phylogenetic approaches to natural product structure prediction. In: Hopwood DA, editor. Methods in Enzymology. Acadamic Press; 2012. pp. 161–182.

134  Katoh K, Standley DM. MAFFT multiple sequence alignment software version 7: improvements in performance and usability. Mol Biol Evol 2013; 30: 772-780.
| Crossref | Google Scholar | PubMed |

135  Thompson JD, Higgins DG, Gibson TJ. CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res 1994; 22: 4673-4680.
| Crossref | Google Scholar | PubMed |

136  Edgar RC. MUSCLE: multiple sequence alignment with high accuracy and high throughput. Nucleic Acids Res 2004; 32: 1792-1797.
| Crossref | Google Scholar | PubMed |

137  Hall T, Biosciences I, Carlsbad C. BioEdit: an important software for molecular biology. GERF Bull Biosci 2011; 2: 60-61.
| Google Scholar |

138  Sharma PL, Das D, Singh N, Giri SJ. The evolution of genome mining tools in microbes and the role of integrated approach in search for novel drug targets. In: Parray JA, Singh N, Li W-J, editors. Host Adaptation, Virulence, and Evolution. Acadamic Press; 2025. pp. 417–433.

139  Stamatakis A. RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies. Bioinformatics 2014; 30: 1312-1313.
| Crossref | Google Scholar | PubMed |

140  Huelsenbeck JP, Ronquist F. MRBAYES: Bayesian inference of phylogenetic trees. Bioinformatics 2001; 17: 754-755.
| Crossref | Google Scholar | PubMed |

141  Ronquist F, Teslenko M, van der Mark P, Ayres DL, Darling A, Höhna S, Larget B, Liu L, Suchard MA, Huelsenbeck JP. MrBayes 3.2: efficient Bayesian phylogenetic inference and model choice across a large model space. Systematic Biology 2012; 61(3): 539-542.
| Crossref | Google Scholar |

142  Guindon S, Dufayard J-F, Lefort V, Anisimova M, Hordijk W, Gascuel O. New algorithms and methods to estimate maximum-likelihood phylogenies: assessing the performance of PhyML 3.0. Syst Biol 2010; 59: 307-321.
| Crossref | Google Scholar | PubMed |

143  Albarano L, Esposito R, Ruocco N, Costantini M. Genome Mining as new challenge in natural products discovery. Mar Drugs 2020; 18: 199.
| Crossref | Google Scholar | PubMed |

144  Valenzuela L, Chi A, Beard S, Orell A, Guiliani N, Shabanowitz J, et al. Genomics, metagenomics and proteomics in biomining microorganisms. Biotechnol Adv 2006; 24: 197-211.
| Crossref | Google Scholar | PubMed |

145  Strehlow BW, Schuster A, Francis WR, Canfield DE. Metagenomic data for Halichondria panicea from Illumina and nanopore sequencing and preliminary genome assemblies for the sponge and two microbial symbionts. BMC Res Notes 2022; 15: 135.
| Crossref | Google Scholar | PubMed |

146  Li D, Liu C-M, Luo R, Sadakane K, Lam T-W. MEGAHIT: an ultra-fast single-node solution for large and complex metagenomics assembly via succinct de Bruijn graph. Bioinform 2015; 31: 1674-1676.
| Crossref | Google Scholar |

147  Nurk S, Meleshko D, Korobeynikov A, Pevzner PA. metaSPAdes: a new versatile metagenomic assembler. Genome Res 2017; 27: 824-834.
| Crossref | Google Scholar | PubMed |

148  Blin K, Shaw S, Kloosterman AM, Charlop-Powers Z, van Wezel GP, Medema H, et al. antiSMASH 6.0: improving cluster detection and comparison capabilities. Nucleic Acids Res 2021; 49: W29-W35.
| Crossref | Google Scholar | PubMed |

149  de Jong A, van Hijum SA, Bijlsma JJ, Kok J, Kuipers OP. BAGEL: a web-based bacteriocin genome mining tool. Nucleic Acids Res 2006; 34: W273-W279.
| Crossref | Google Scholar | PubMed |

150  Merwin NJ, Mousa WK, Dejong CA, Skinnider MA, Cannon MJ, Li H, et al. DeepRiPP integrates multiomics data to automate discovery of novel ribosomally synthesized natural products. Proc Natl Acad Sci 2020; 117: 371-380.
| Crossref | Google Scholar | PubMed |

151  Skinnider MA, Merwin NJ, Johnston CW, Magarvey NA. PRISM 3: expanded prediction of natural product chemical structures from microbial genomes. Nucleic Acids Res 2017; 45: W49-W54.
| Crossref | Google Scholar | PubMed |

152  Kloosterman AM, Medema MH, van Wezel GP. Omics-based strategies to discover novel classes of RiPP natural products. Curr Opin Biotechnol 2021; 69: 60-67.
| Crossref | Google Scholar | PubMed |

153  Santos-Aberturas J, Chandra G, Frattaruolo L, Lacret R, Pham TH, Vior NM, et al. Uncovering the unexplored diversity of thioamidated ribosomal peptides in Actinobacteria using the RiPPER genome mining tool. Nucleic Acids Res 2019; 47: 4624-4637.
| Crossref | Google Scholar | PubMed |

154  de los Santos ELC. NeuRiPP: neural network identification of RiPP precursor peptides. Sci Rep 2019; 9: 13406.
| Crossref | Google Scholar | PubMed |

155  Oliveira RS, Pinto OH, Quirino BF, de Freitas MA, Thompson FL, Thompson C, et al. Genome-resolved metagenomic analysis of Great Amazon Reef System sponge-associated Latescibacterota bacteria and their potential contributions to the host sponge and reef. Front Microbiomes 2023; 2: 1206961.
| Crossref | Google Scholar |

156  Parks DH, Rinke C, Chuvochina M, Chaumeil P-A, Woodcroft BJ, Evans PN, et al. Recovery of nearly 8,000 metagenome-assembled genomes substantially expands the tree of life. Nat Microbiol 2017; 2: 1533-1542.
| Crossref | Google Scholar | PubMed |

157  Nguyen NA, Lin Z, Mohanty I, Garg N, Schmidt EW, Agarwal V. An obligate peptidyl brominase underlies the discovery of highly distributed biosynthetic gene clusters in marine sponge microbiomes. J Am Chem Soc 2021; 143: 10221-10231.
| Crossref | Google Scholar | PubMed |

158  Loureiro C, Galani A, Gavriilidou A, Chaib de Mares M, van der Oost J, Medema H, et al. Comparative metagenomic analysis of biosynthetic diversity across sponge microbiomes highlights metabolic novelty, conservation, and diversification. mSystems 2022; 7: e0035722.
| Crossref | Google Scholar | PubMed |

159  Gomez-Escribano JP, Bibb MJ. Engineering Streptomyces coelicolor for heterologous expression of secondary metabolite gene clusters. Microb Biotechnol 2011; 4: 207-215.
| Crossref | Google Scholar | PubMed |

160  Zhang Y, Chen M, Bruner SD, Ding Y. Heterologous production of microbial ribosomally synthesized and post-translationally modified peptides. Front Microbiol 2018; 9: 1801.
| Crossref | Google Scholar | PubMed |

161  Wang M, Carver JJ, Phelan VV, Sanchez LM, Garg N, Peng Y, et al. Sharing and community curation of mass spectrometry data with Global Natural Products Social molecular networking. Nat Biotechnol 2016; 34: 828-837.
| Crossref | Google Scholar | PubMed |

162  Cárdenas P, Xavier JR, Reveillaud J, Schander C, Rapp HT. Molecular phylogeny of the Astrophorida (Porifera, Demospongiaep) reveals an unexpected high level of spicule homoplasy. PLoS ONE 2011; 6: e18318.
| Crossref | Google Scholar | PubMed |

163  Cárdenas P. Who produces ianthelline? The arctic sponge Stryphnus fortis or its sponge epibiont Hexadella dedritifera: a probable case of sponge–sponge contamination. J Chem Ecol 2016; 42: 339-347.
| Crossref | Google Scholar | PubMed |

164  Cárdenas P, Gamage J, Hettiarachchi CM, Gunasekera S. Good practices in sponge natural product studies: revising vouchers with isomalabaricane triterpenes. Mar Drugs 2022; 20: 190.
| Crossref | Google Scholar | PubMed |

165  Riesgo A, Farrar N, Windsor PJ, Giribet G, Leys SP. The analysis of eight transcriptomes from all poriferan classes reveals surprising genetic complexity in sponges. Mol Biol Evol 2014; 31: 1102-1120.
| Crossref | Google Scholar | PubMed |

166  Nowak VV, Hou P, Owen JG. Microbial communities associated with marine sponges from diverse geographic locations harbor biosynthetic novelty. Appl Environ Microbiol 2024; 90(12): e0072624.
| Crossref | Google Scholar | PubMed |