Characterization of the N-acetyl-α-D-glucosaminyl L-malate Synthase and Deacetylase Functions for Bacillithiol Biosynthesis in Bacillus Anthracis
Overview
Authors
Affiliations
Bacillithiol (Cys-GlcN-malate, BSH) has recently been identified as a novel low-molecular weight thiol in Bacillus anthracis, Staphylococcus aureus, and several other Gram-positive bacteria lacking glutathione and mycothiol. We have now characterized the first two enzymes for the BSH biosynthetic pathway in B. anthracis, which combine to produce α-d-glucosaminyl l-malate (GlcN-malate) from UDP-GlcNAc and l-malate. The structure of the GlcNAc-malate intermediate has been determined, as have the kinetic parameters for the BaBshA glycosyltransferase (→GlcNAc-malate) and the BaBshB deacetylase (→GlcN-malate). BSH is one of only two natural products reported to contain a malyl glycoside, and the crystal structure of the BaBshA-UDP-malate ternary complex, determined in this work at 3.3 Å resolution, identifies several active-site interactions important for the specific recognition of l-malate, but not other α-hydroxy acids, as the acceptor substrate. In sharp contrast to the structures reported for the GlcNAc-1-d-myo-inositol-3-phosphate synthase (MshA) apo and ternary complex forms, there is no major conformational change observed in the structures of the corresponding BaBshA forms. A mutant strain of B. anthracis deficient in the BshA glycosyltransferase fails to produce BSH, as predicted. This B. anthracis bshA locus (BA1558) has been identified in a transposon-site hybridization study as required for growth, sporulation, or germination [Day, W. A., Jr., Rasmussen, S. L., Carpenter, B. M., Peterson, S. N., and Friedlander, A. M. (2007) J. Bacteriol. 189, 3296-3301], suggesting that the biosynthesis of BSH could represent a target for the development of novel antimicrobials with broad-spectrum activity against Gram-positive pathogens like B. anthracis. The metabolites that function in thiol redox buffering and homeostasis in Bacillus are not well understood, and we present a composite picture based on this and other recent work.
Sulfinamide Formation from the Reaction of Bacillithiol and Nitroxyl.
Negrellos A, Rice A, Dos Santos P, King S ACS Chem Biol. 2023; 18(12):2524-2534.
PMID: 38012810 PMC: 11229778. DOI: 10.1021/acschembio.3c00526.
Ireland K, Kayrouz C, Huang J, Seyedsayamdost M, Davis K Biochemistry. 2023; 62(23):3337-3342.
PMID: 37966244 PMC: 10702425. DOI: 10.1021/acs.biochem.3c00452.
Paudel S, Wachira J, McCarthy P Processes (Basel). 2023; 9(12).
PMID: 37483532 PMC: 10361700. DOI: 10.3390/pr9122192.
Xie S, Huang Q, Tan R, Zhang W, Qi Q, Lu X Appl Environ Microbiol. 2022; 88(20):e0107622.
PMID: 36197104 PMC: 9599414. DOI: 10.1128/aem.01076-22.
Rawat M, Maupin-Furlow J Antioxidants (Basel). 2020; 9(5).
PMID: 32380716 PMC: 7278568. DOI: 10.3390/antiox9050381.