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Genomics-Driven Discovery of Benzoxazole Alkaloids from the Marine-Derived Micromonospora sp. SCSIO 07395

Benzoxazole alkaloids exhibit a diverse array of structures and interesting biological activities. Herein we report the identification of a benzoxazole alkaloid-encoding biosynthetic gene cluster (mich BGC) in the marine-derived actinomycete Micromonospora sp. SCSIO 07395 and the heterologous expres...

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Detalles Bibliográficos
Autores principales: Cheng, Ziqian, Zhang, Qingbo, Peng, Jing, Zhao, Xiaoyang, Ma, Liang, Zhang, Changsheng, Zhu, Yiguang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9864271/
https://www.ncbi.nlm.nih.gov/pubmed/36677886
http://dx.doi.org/10.3390/molecules28020821
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author Cheng, Ziqian
Zhang, Qingbo
Peng, Jing
Zhao, Xiaoyang
Ma, Liang
Zhang, Changsheng
Zhu, Yiguang
author_facet Cheng, Ziqian
Zhang, Qingbo
Peng, Jing
Zhao, Xiaoyang
Ma, Liang
Zhang, Changsheng
Zhu, Yiguang
author_sort Cheng, Ziqian
collection PubMed
description Benzoxazole alkaloids exhibit a diverse array of structures and interesting biological activities. Herein we report the identification of a benzoxazole alkaloid-encoding biosynthetic gene cluster (mich BGC) in the marine-derived actinomycete Micromonospora sp. SCSIO 07395 and the heterologous expression of this BGC in Streptomyces albus. This approach led to the discovery of five new benzoxazole alkaloids microechmycin A–E (1–5), and a previously synthesized compound 6. Their structures were elucidated by HRESIMS and 1D and 2D NMR data. Microechmycin A (1) showed moderate antibacterial activity against Micrococcus luteus SCSIO ML01 with the minimal inhibitory concentration (MIC) value of 8 μg mL(−1).
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spelling pubmed-98642712023-01-22 Genomics-Driven Discovery of Benzoxazole Alkaloids from the Marine-Derived Micromonospora sp. SCSIO 07395 Cheng, Ziqian Zhang, Qingbo Peng, Jing Zhao, Xiaoyang Ma, Liang Zhang, Changsheng Zhu, Yiguang Molecules Article Benzoxazole alkaloids exhibit a diverse array of structures and interesting biological activities. Herein we report the identification of a benzoxazole alkaloid-encoding biosynthetic gene cluster (mich BGC) in the marine-derived actinomycete Micromonospora sp. SCSIO 07395 and the heterologous expression of this BGC in Streptomyces albus. This approach led to the discovery of five new benzoxazole alkaloids microechmycin A–E (1–5), and a previously synthesized compound 6. Their structures were elucidated by HRESIMS and 1D and 2D NMR data. Microechmycin A (1) showed moderate antibacterial activity against Micrococcus luteus SCSIO ML01 with the minimal inhibitory concentration (MIC) value of 8 μg mL(−1). MDPI 2023-01-13 /pmc/articles/PMC9864271/ /pubmed/36677886 http://dx.doi.org/10.3390/molecules28020821 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Cheng, Ziqian
Zhang, Qingbo
Peng, Jing
Zhao, Xiaoyang
Ma, Liang
Zhang, Changsheng
Zhu, Yiguang
Genomics-Driven Discovery of Benzoxazole Alkaloids from the Marine-Derived Micromonospora sp. SCSIO 07395
title Genomics-Driven Discovery of Benzoxazole Alkaloids from the Marine-Derived Micromonospora sp. SCSIO 07395
title_full Genomics-Driven Discovery of Benzoxazole Alkaloids from the Marine-Derived Micromonospora sp. SCSIO 07395
title_fullStr Genomics-Driven Discovery of Benzoxazole Alkaloids from the Marine-Derived Micromonospora sp. SCSIO 07395
title_full_unstemmed Genomics-Driven Discovery of Benzoxazole Alkaloids from the Marine-Derived Micromonospora sp. SCSIO 07395
title_short Genomics-Driven Discovery of Benzoxazole Alkaloids from the Marine-Derived Micromonospora sp. SCSIO 07395
title_sort genomics-driven discovery of benzoxazole alkaloids from the marine-derived micromonospora sp. scsio 07395
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9864271/
https://www.ncbi.nlm.nih.gov/pubmed/36677886
http://dx.doi.org/10.3390/molecules28020821
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