Open Access
Open access
Molecules, volume 25, issue 19, pages 4446

Hetiamacin E and F, New amicoumacin antibiotics from bacillus subtilis PJS using MS/MS-based molecular networking

Wang Ting 1, 2
Lu Qinpei 1, 2
Sun Chenghang 1, 2
Osterman Ilya A 3, 4
Hu Xinxin 1, 2
You Xuefu 1, 2
Liu Shaowei 1, 2
Wu Gang 1, 2
Publication typeJournal Article
Publication date2020-09-27
Journal: Molecules
Quartile SCImago
Q1
Quartile WOS
Q2
Impact factor4.6
ISSN14203049
Organic Chemistry
Drug Discovery
Physical and Theoretical Chemistry
Pharmaceutical Science
Molecular Medicine
Analytical Chemistry
Chemistry (miscellaneous)
Abstract

To combat escalating levels of antibiotic resistance, novel strategies are developed to address the everlasting demand for new antibiotics. This study aimed at investigating amicoumacin antibiotics from the desert-derived Bacillus subtilis PJS by using the modern MS/MS-based molecular networking approach. Two new amicoumacins, namely hetiamacin E (1) and hetiamacin F (2), were finally isolated. The planar structures were determined by analysis of extensive NMR spectroscopic and HR–ESI–MS data, and the absolute configurations were concluded by analysis of the CD spectrum. Hetiamacin E (1) showed strong antibacterial activities against methicillin-sensitive and resistant Staphylococcus epidermidis at 2–4 µg/mL, and methicillin-sensitive and resistant Staphylococcus aureus at 8–16 µg/mL. Hetiamacin F (2) exhibited moderate antibacterial activities against Staphylococcus sp. at 32 µg/mL. Both compounds were inhibitors of protein biosynthesis demonstrated by a double fluorescent protein reporter system.

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GOST |
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GOST Copy
Wang T. et al. Hetiamacin E and F, New amicoumacin antibiotics from bacillus subtilis PJS using MS/MS-based molecular networking // Molecules. 2020. Vol. 25. No. 19. p. 4446.
GOST all authors (up to 50) Copy
Wang T., Lu Q., Sun C., Lukianov D., Osterman I. A., Sergiev P. V., Dontsova O. A., Hu X., You X., Liu S., Wu G. Hetiamacin E and F, New amicoumacin antibiotics from bacillus subtilis PJS using MS/MS-based molecular networking // Molecules. 2020. Vol. 25. No. 19. p. 4446.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.3390/molecules25194446
UR - https://doi.org/10.3390%2Fmolecules25194446
TI - Hetiamacin E and F, New amicoumacin antibiotics from bacillus subtilis PJS using MS/MS-based molecular networking
T2 - Molecules
AU - Lu, Qinpei
AU - Lukianov, Dmitrii
AU - Sergiev, Petr Vladimirovich
AU - Dontsova, Olga Anatolievna
AU - Hu, Xinxin
AU - Liu, Shaowei
AU - Wang, Ting
AU - Wu, Gang
AU - Sun, Chenghang
AU - Osterman, Ilya A
AU - You, Xuefu
PY - 2020
DA - 2020/09/27 00:00:00
PB - Multidisciplinary Digital Publishing Institute (MDPI)
SP - 4446
IS - 19
VL - 25
PMID - 32992672
SN - 1420-3049
ER -
BibTex |
Cite this
BibTex Copy
@article{2020_Wang,
author = {Qinpei Lu and Dmitrii Lukianov and Petr Vladimirovich Sergiev and Olga Anatolievna Dontsova and Xinxin Hu and Shaowei Liu and Ting Wang and Gang Wu and Chenghang Sun and Ilya A Osterman and Xuefu You},
title = {Hetiamacin E and F, New amicoumacin antibiotics from bacillus subtilis PJS using MS/MS-based molecular networking},
journal = {Molecules},
year = {2020},
volume = {25},
publisher = {Multidisciplinary Digital Publishing Institute (MDPI)},
month = {sep},
url = {https://doi.org/10.3390%2Fmolecules25194446},
number = {19},
pages = {4446},
doi = {10.3390/molecules25194446}
}
MLA
Cite this
MLA Copy
Wang, Ting, et al. “Hetiamacin E and F, New amicoumacin antibiotics from bacillus subtilis PJS using MS/MS-based molecular networking.” Molecules, vol. 25, no. 19, Sep. 2020, p. 4446. https://doi.org/10.3390%2Fmolecules25194446.
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