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Streptomyces tardus sp. nov.: A Slow-Growing Actinobacterium Producing Candicidin, Isolated From Sediments of the Trondheim Fjord
Marine environments are home to an extensive number of microorganisms, many of which remain unexplored for taxonomic novelty and functional capabilities. In this study, a slow-growing Streptomyces strain expressing unique genomic and phenotypic characteristics, P38-E01(T), was described using a poly...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8371330/ https://www.ncbi.nlm.nih.gov/pubmed/34421874 http://dx.doi.org/10.3389/fmicb.2021.714233 |
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author | Králová, Stanislava Sandoval-Powers, Megan Fawwal, Dorelle V. Degnes, Kristin F. Lewin, Anna Sofia Klinkenberg, Geir Nguyen, Giang-Son Liles, Mark R. Wentzel, Alexander |
author_facet | Králová, Stanislava Sandoval-Powers, Megan Fawwal, Dorelle V. Degnes, Kristin F. Lewin, Anna Sofia Klinkenberg, Geir Nguyen, Giang-Son Liles, Mark R. Wentzel, Alexander |
author_sort | Králová, Stanislava |
collection | PubMed |
description | Marine environments are home to an extensive number of microorganisms, many of which remain unexplored for taxonomic novelty and functional capabilities. In this study, a slow-growing Streptomyces strain expressing unique genomic and phenotypic characteristics, P38-E01(T), was described using a polyphasic taxonomic approach. This strain is part of a collection of over 8,000 marine Actinobacteria isolates collected in the Trondheim fjord of Norway by SINTEF Industry (Trondheim, Norway) and the Norwegian University of Science and Technology (NTNU, Trondheim, Norway). Strain P38-E01(T) was isolated from the sediments of the Trondheim fjord, and phylogenetic analyses affiliated this strain with the genus Streptomyces, but it was not closely affiliated with other described species. The closest related type strains were Streptomyces daliensis YIM 31724(T) (98.6%), Streptomyces rimosus subsp. rimosus ATCC 10970(T) (98.4%), and Streptomyces sclerotialus NRRL ISP-5269(T) (98.3%). Predominant fatty acids were C(16:0) iso, C(16:0), and Summed Feature 3, and the predominant respiratory quinones were MK-10(H(6)), MK-10(H(4)), and MK9(H(4)). The main polar lipids were identified as diphosphatidylglycerol, phosphatidylethanolamine, phosphatidylglycerol, and phosphoglycolipid. The whole-cell sugars were glucose, ribose, and in minor amounts, mannose. The cell wall peptidoglycan contained LL-diaminopimelic acid. The draft genome has a size of 6.16 Mb, with a %G + C content of 71.4% and is predicted to contain at least 19 biosynthetic gene clusters encoding diverse secondary metabolites. Strain P38-E01(T) was found to inhibit the growth of the pathogenic yeast Candida albicans ATCC 90028 and a number of Gram-positive bacterial human and plant pathogens. Metabolites extracted from cultures of P38-E01(T) were analyzed by mass spectrometry, and it was found that the isolate produced the antifungal compound candicidin. Phenotypic and chemotaxonomic signatures, along with phylogenetic analyses, distinguished isolate P38-E01(T) from its closest neighbors; thus, this isolate represents a novel species of the genus Streptomyces for which the name Streptomyces tardus sp. nov. (P38-E01(T) = CCM 9049(T) = DSM 111582(T)) is proposed. |
format | Online Article Text |
id | pubmed-8371330 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-83713302021-08-19 Streptomyces tardus sp. nov.: A Slow-Growing Actinobacterium Producing Candicidin, Isolated From Sediments of the Trondheim Fjord Králová, Stanislava Sandoval-Powers, Megan Fawwal, Dorelle V. Degnes, Kristin F. Lewin, Anna Sofia Klinkenberg, Geir Nguyen, Giang-Son Liles, Mark R. Wentzel, Alexander Front Microbiol Microbiology Marine environments are home to an extensive number of microorganisms, many of which remain unexplored for taxonomic novelty and functional capabilities. In this study, a slow-growing Streptomyces strain expressing unique genomic and phenotypic characteristics, P38-E01(T), was described using a polyphasic taxonomic approach. This strain is part of a collection of over 8,000 marine Actinobacteria isolates collected in the Trondheim fjord of Norway by SINTEF Industry (Trondheim, Norway) and the Norwegian University of Science and Technology (NTNU, Trondheim, Norway). Strain P38-E01(T) was isolated from the sediments of the Trondheim fjord, and phylogenetic analyses affiliated this strain with the genus Streptomyces, but it was not closely affiliated with other described species. The closest related type strains were Streptomyces daliensis YIM 31724(T) (98.6%), Streptomyces rimosus subsp. rimosus ATCC 10970(T) (98.4%), and Streptomyces sclerotialus NRRL ISP-5269(T) (98.3%). Predominant fatty acids were C(16:0) iso, C(16:0), and Summed Feature 3, and the predominant respiratory quinones were MK-10(H(6)), MK-10(H(4)), and MK9(H(4)). The main polar lipids were identified as diphosphatidylglycerol, phosphatidylethanolamine, phosphatidylglycerol, and phosphoglycolipid. The whole-cell sugars were glucose, ribose, and in minor amounts, mannose. The cell wall peptidoglycan contained LL-diaminopimelic acid. The draft genome has a size of 6.16 Mb, with a %G + C content of 71.4% and is predicted to contain at least 19 biosynthetic gene clusters encoding diverse secondary metabolites. Strain P38-E01(T) was found to inhibit the growth of the pathogenic yeast Candida albicans ATCC 90028 and a number of Gram-positive bacterial human and plant pathogens. Metabolites extracted from cultures of P38-E01(T) were analyzed by mass spectrometry, and it was found that the isolate produced the antifungal compound candicidin. Phenotypic and chemotaxonomic signatures, along with phylogenetic analyses, distinguished isolate P38-E01(T) from its closest neighbors; thus, this isolate represents a novel species of the genus Streptomyces for which the name Streptomyces tardus sp. nov. (P38-E01(T) = CCM 9049(T) = DSM 111582(T)) is proposed. Frontiers Media S.A. 2021-08-04 /pmc/articles/PMC8371330/ /pubmed/34421874 http://dx.doi.org/10.3389/fmicb.2021.714233 Text en Copyright © 2021 Králová, Sandoval-Powers, Fawwal, Degnes, Lewin, Klinkenberg, Nguyen, Liles and Wentzel. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Microbiology Králová, Stanislava Sandoval-Powers, Megan Fawwal, Dorelle V. Degnes, Kristin F. Lewin, Anna Sofia Klinkenberg, Geir Nguyen, Giang-Son Liles, Mark R. Wentzel, Alexander Streptomyces tardus sp. nov.: A Slow-Growing Actinobacterium Producing Candicidin, Isolated From Sediments of the Trondheim Fjord |
title | Streptomyces tardus sp. nov.: A Slow-Growing Actinobacterium Producing Candicidin, Isolated From Sediments of the Trondheim Fjord |
title_full | Streptomyces tardus sp. nov.: A Slow-Growing Actinobacterium Producing Candicidin, Isolated From Sediments of the Trondheim Fjord |
title_fullStr | Streptomyces tardus sp. nov.: A Slow-Growing Actinobacterium Producing Candicidin, Isolated From Sediments of the Trondheim Fjord |
title_full_unstemmed | Streptomyces tardus sp. nov.: A Slow-Growing Actinobacterium Producing Candicidin, Isolated From Sediments of the Trondheim Fjord |
title_short | Streptomyces tardus sp. nov.: A Slow-Growing Actinobacterium Producing Candicidin, Isolated From Sediments of the Trondheim Fjord |
title_sort | streptomyces tardus sp. nov.: a slow-growing actinobacterium producing candicidin, isolated from sediments of the trondheim fjord |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8371330/ https://www.ncbi.nlm.nih.gov/pubmed/34421874 http://dx.doi.org/10.3389/fmicb.2021.714233 |
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