Bacillamidins A–G from a Marine-Derived Bacillus pumilus
Seven long-chain amides, including five previously undescribed bacillamidins A–E (1–5) and two previously reported synthetic analogs, bacillamidins F (6) and G (7), were isolated from extracts of the marine-derived Bacillus pumilus strain RJA1515. The structures of the new compou...
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doaj-2295c7aa517d4d4c8476bbe3abdc86772020-11-24T21:14:36ZengMDPI AGMarine Drugs1660-33972018-09-0116932610.3390/md16090326md16090326Bacillamidins A–G from a Marine-Derived Bacillus pumilusSi-Yu Zhou0Yi-Jie Hu1Fan-Cheng Meng2Shen-Yue Qu3Rui Wang4Raymond J. Andersen5Zhi-Hua Liao6Min Chen7Key Laboratory of Luminescent and Real-Time Analytical Chemistry (Ministry of Education), College of Pharmaceutical Sciences, Southwest University, Chongqing 400715, ChinaKey Laboratory of Luminescent and Real-Time Analytical Chemistry (Ministry of Education), College of Pharmaceutical Sciences, Southwest University, Chongqing 400715, ChinaKey Laboratory of Luminescent and Real-Time Analytical Chemistry (Ministry of Education), College of Pharmaceutical Sciences, Southwest University, Chongqing 400715, ChinaKey Laboratory of Luminescent and Real-Time Analytical Chemistry (Ministry of Education), College of Pharmaceutical Sciences, Southwest University, Chongqing 400715, ChinaKey Laboratory of Luminescent and Real-Time Analytical Chemistry (Ministry of Education), College of Pharmaceutical Sciences, Southwest University, Chongqing 400715, ChinaDepartment of Chemistry, University of British Columbia, Vancouver, BC V6T1Z1, CanadaSchool of Life Sciences, Southwest University, Chongqing 400715, ChinaKey Laboratory of Luminescent and Real-Time Analytical Chemistry (Ministry of Education), College of Pharmaceutical Sciences, Southwest University, Chongqing 400715, ChinaSeven long-chain amides, including five previously undescribed bacillamidins A–E (1–5) and two previously reported synthetic analogs, bacillamidins F (6) and G (7), were isolated from extracts of the marine-derived Bacillus pumilus strain RJA1515. The structures of the new compounds were established by extensive analysis of 1D and 2D nuclear magnetic resonance (NMR) data as well as high resolution mass spectrometry (HRMS), and the absolute configurations of the stereogenic carbons of 1–4 were established by comparison of the calculated and the experimental electronic circular dichroism (ECD) spectra. The cytotoxic and antimicrobial activities of 1–7 were evaluated.http://www.mdpi.com/1660-3397/16/9/326Bacillus pumiluslong-chain amidescytotoxic activityantimicrobial activity |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Si-Yu Zhou Yi-Jie Hu Fan-Cheng Meng Shen-Yue Qu Rui Wang Raymond J. Andersen Zhi-Hua Liao Min Chen |
spellingShingle |
Si-Yu Zhou Yi-Jie Hu Fan-Cheng Meng Shen-Yue Qu Rui Wang Raymond J. Andersen Zhi-Hua Liao Min Chen Bacillamidins A–G from a Marine-Derived Bacillus pumilus Marine Drugs Bacillus pumilus long-chain amides cytotoxic activity antimicrobial activity |
author_facet |
Si-Yu Zhou Yi-Jie Hu Fan-Cheng Meng Shen-Yue Qu Rui Wang Raymond J. Andersen Zhi-Hua Liao Min Chen |
author_sort |
Si-Yu Zhou |
title |
Bacillamidins A–G from a Marine-Derived Bacillus pumilus |
title_short |
Bacillamidins A–G from a Marine-Derived Bacillus pumilus |
title_full |
Bacillamidins A–G from a Marine-Derived Bacillus pumilus |
title_fullStr |
Bacillamidins A–G from a Marine-Derived Bacillus pumilus |
title_full_unstemmed |
Bacillamidins A–G from a Marine-Derived Bacillus pumilus |
title_sort |
bacillamidins a–g from a marine-derived bacillus pumilus |
publisher |
MDPI AG |
series |
Marine Drugs |
issn |
1660-3397 |
publishDate |
2018-09-01 |
description |
Seven long-chain amides, including five previously undescribed bacillamidins A–E (1–5) and two previously reported synthetic analogs, bacillamidins F (6) and G (7), were isolated from extracts of the marine-derived Bacillus pumilus strain RJA1515. The structures of the new compounds were established by extensive analysis of 1D and 2D nuclear magnetic resonance (NMR) data as well as high resolution mass spectrometry (HRMS), and the absolute configurations of the stereogenic carbons of 1–4 were established by comparison of the calculated and the experimental electronic circular dichroism (ECD) spectra. The cytotoxic and antimicrobial activities of 1–7 were evaluated. |
topic |
Bacillus pumilus long-chain amides cytotoxic activity antimicrobial activity |
url |
http://www.mdpi.com/1660-3397/16/9/326 |
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