» Articles » PMID: 8002387

Pyrroindomycins, Novel Antibiotics Produced by Streptomyces Rugosporus Sp. LL-42D005. I. Isolation and Structure Determination

Overview
Date 1994 Nov 1
PMID 8002387
Citations 13
Authors
Affiliations
Soon will be listed here.
Abstract

Pyrroindomycins A and B were isolated from fermentations of culture LL-42D005, a strain of Streptomyces rugosporus. Pyrroindomycins possess potent antimicrobial activities against methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococci. Their structures have been determined by using 1- and 2-D NMR, mass spectroscopy and chemical degradations. Pyrroindomycins are the first natural products that contain the highly unsaturated pyrroloindole moiety.

Citing Articles

Mechanism of the Stereoselective Catalysis of Diels-Alderase PyrE3 Involved in Pyrroindomycin Biosynthesis.

Li B, Guan X, Yang S, Zou Y, Liu W, Houk K J Am Chem Soc. 2022; 144(11):5099-5107.

PMID: 35258962 PMC: 9292823. DOI: 10.1021/jacs.2c00015.


Computational Investigation of the Mechanism of Diels-Alderase PyrI4.

Zou Y, Yang S, Sanders J, Li W, Yu P, Wang H J Am Chem Soc. 2020; 142(47):20232-20239.

PMID: 33190496 PMC: 9328771. DOI: 10.1021/jacs.0c10813.


The crystal structure of AbsH3: A putative flavin adenine dinucleotide-dependent reductase in the abyssomicin biosynthesis pathway.

Clinger J, Wang X, Cai W, Zhu Y, Miller M, Zhan C Proteins. 2020; 89(1):132-137.

PMID: 32852843 PMC: 7910320. DOI: 10.1002/prot.25994.


Computational Insights into an Enzyme-Catalyzed [4+2] Cycloaddition.

Zheng Y, Thiel W J Org Chem. 2017; 82(24):13563-13571.

PMID: 29131960 PMC: 5735378. DOI: 10.1021/acs.joc.7b02794.


Natural [4 + 2]-Cyclases.

Jeon B, Wang S, Ruszczycky M, Liu H Chem Rev. 2017; 117(8):5367-5388.

PMID: 28441874 PMC: 6063532. DOI: 10.1021/acs.chemrev.6b00578.