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Genomics and metabolomics-based assessment of the biosynthetic potential of the sponge-associated microorganism Streptomyces cacaoi strain R2A-843A from the Philippines

dc.citation.journaltitleScience and Engineering Journal
dc.contributor.authorMalto, Zabrina Bernice L.
dc.contributor.authorReyes, Joeriggo M.
dc.contributor.authorLo, Bernard Isaiah
dc.contributor.authorDavis, Kevin Bossie S.
dc.contributor.authorConcepcion, Gisela
dc.contributor.authorSalvador-Reyes, Lilibeth A.
dc.date.accessioned2025-03-30T11:35:45Z
dc.date.issued2023-10-20
dc.descriptionThe authors acknowledge funding support from the Department of Science and Technology - Philippine Council for Health Research and Development through the Discovery and Development of Health Products - Marine Component Program. Genome sequencing was made possible through the CHEDPCARI IHITM63 Project. We thank Ms. Shalice R. SusanaGuevarra for conducting the bioactivity assay. This work was done under the supervision of the Bureau of Fisheries and Aquatic Resources under Gratuitous Permit No. FBP-0035-10. This is MSI Contribution No. 501.
dc.description.abstractThe biosynthetic machinery of the sponge-associated Streptomyces cacaoi strain R2A-843A was assessed using a combined genomics and metabolomics approach. Whole genome sequencing and molecular networking showed the high biosynthetic potential of this actinomycete. A significant proportion of the genome is dedicated to secondary metabolite production, with biosynthetic gene clusters for nonribosomal peptides, polyketides, and terpenes being the most represented. Seven cyclic pentapeptides, including a putative new analogue, and a glycosylated lanthipeptide were identified using HRMS and untargeted MS/MS analysis. To validate our genome and metabolome analysis, we undertook a mass spectrometry-guided purification and confirmed the production of the known peptides BE-18257A (1) and BE-18257B (2). The production of 1 and 2 and the growth of the microorganism were monitored for eight days. Compound 2 was produced at a higher concentration, starting at 48 h post-incubation. Both compounds were noncytotoxic against colorectal and breast cancer cell lines.
dc.identifier.citationMalto, Z. B. L., Reyes, J. M., Lo, B. I. D., Davis, K. B. S., Concepcion, G. P., & Salvador-Reyes, L. A. (2023). Genomics and metabolomics-based assessment of the biosynthetic potential of the sponge-associated microorganism Streptomyces cacaoi strain R2A-843A from the Philippines. Science and Engineering Journal, 16 (Supplement), 67-89.
dc.identifier.doi10.54645/mffr36805
dc.identifier.issn2799-189X
dc.identifier.urihttps://hdl.handle.net/20.500.14697/211
dc.language.isoen
dc.publisherPhilippine-American Academy of Science and Engineering
dc.relation.urihttps://scienggj.org/2023/2023%20Special%20Issue/8/SciEnggJ%202023%20Special%20Issue%2067-89-Malto%20et%20al.pdf
dc.subjectBiosynthesis
dc.subject.agrovocgenomics
dc.subject.agrovocmetabolomics
dc.subject.agrovocsponges
dc.subject.agrovocStreptomyces
dc.subject.lcshGenomics
dc.subject.lcshSponges
dc.subject.lcshActinobacteria
dc.subject.lcshMetabolites
dc.subject.lcshStreptomyces
dc.subject.lcshMicrobial metabolites
dc.subject.lcshBiosynthesis
dc.subject.odcChallenge 6: Increase community resilience to ocean hazards
dc.subject.odcChallenge 7: Expand the Global Ocean Observing System
dc.subject.odcChallenge 9: Skills, knowledge, and technology for all
dc.subject.sdgSDG 3 - Good health and well-being
dc.subject.sdgSDG 14 - Life below water
dc.subject.sdgSDG 9 - Industry, innovation and infrastructure
dc.titleGenomics and metabolomics-based assessment of the biosynthetic potential of the sponge-associated microorganism Streptomyces cacaoi strain R2A-843A from the Philippines
dc.typeArticle
local.subjectActinobacteria
local.subjectBE-18257
local.subjectgenome
local.subjectmetabolome
local.subjectpentaminomycins
local.subjectStreptomyces
local.subjectsecondary metabolites
local.subject.scientificnameStreptomyces
local.subject.scientificnameStreptomyces cacaoi
oaire.citation.endPage89
oaire.citation.startPage67
oaire.citation.volume16 (Supplement)

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