| Literature DB >> 26374245 |
Yoon Mee Park1, Hwa Jeong Lee1, Jae-Ho Jeong2, Joong-Ki Kook3, Hyon E Choy2, Tae-Wook Hahn4, Iel Soo Bang5.
Abstract
Nitric oxide (NO) inactivates iron-sulfur enzymes in bacterial amino acid biosynthetic pathways, causing amino acid auxotrophy. We demonstrate that exogenous supplementation with branched-chain amino acids (BCAA) can restore the NO resistance of hmp mutant Salmonella Typhimurium lacking principal NO-metabolizing enzyme flavohemoglobin, and of mutants further lacking iron-sulfur enzymes dihydroxy-acid dehydratase (IlvD) and isopropylmalate isomerase (LeuCD) that are essential for BCAA biosynthesis, in an oxygen-dependent manner. BCAA supplementation did not affect the NO consumption rate of S. Typhimurium, suggesting the BCAA-promoted NO resistance independent of NO metabolism. BCAA supplementation also induced intracellular survival of ilvD and leuCD mutants at wild-type levels inside RAW 264.7 macrophages that produce constant amounts of NO regardless of varied supplemental BCAA concentrations. Our results suggest that the NO-induced BCAA auxotrophy of Salmonella, due to inactivation of iron-sulfur enzymes for BCAA biosynthesis, could be rescued by bacterial taking up exogenous BCAA available in oxic environments.Entities:
Keywords: Branched-chain amino acids; Iron-sulfur cluster enzyme; Nitric oxide; Salmonella Typhimurium
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Year: 2015 PMID: 26374245 DOI: 10.1007/s00203-015-1151-y
Source DB: PubMed Journal: Arch Microbiol ISSN: 0302-8933 Impact factor: 2.552