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Originally published In Press as doi:10.1074/jbc.M604724200 on August 28, 2006
J. Biol. Chem., Vol. 281, Issue 45, 33910-33920, November 10, 2006
Biochemistry of the Initial Steps of Mycothiol Biosynthesis*
Gerald L. Newton,
Philong Ta,
Krzysztof P. Bzymek, and
Robert C. Fahey1
From the
Department of Chemistry and Biochemistry, University of California, La Jolla, California 92093
Mycothiol is the major thiol produced by mycobacteria and is required for growth of Mycobacterium tuberculosis. The final three steps in the biosynthesis of mycothiol have been fully elucidated but the initial steps have been unclear. A glycosyltransferase, MshA, is required for production of the mycothiol precursor, 1-O-(2-acetamido-2-deoxy- -D-glucopyranosyl)-D-myo-inositol, but its substrates and immediate products were unknown. In this study, we show that the N-acetylglucosamine donor is UDP-N-acetylglucosamine and that the N-acetylglucosamine acceptor is 1L-myo-inositol 1-phosphate. The reaction generates UDP and 1-O-(2-acetamido-2-deoxy- -D-glucopyranosyl)-D-myo-inositol 3-phosphate. Using cell-free extracts of M. smegmatis mc2155, little activity was obtained with myo-inositol, 1D-myo-inositol 1-phosphate, or myo-inositol 2-phosphate as the N-acetylglucosamine acceptor. A phosphatase, designated MshA2, is required to dephosphorylate 1-O-(2-acetamido-2-deoxy- -glucopyranosyl)-D-myo-inositol 3-phosphate to produce 1-O-(2-acetamido-2-deoxy- -D-glucopyranosyl)-D-myo-inositol. The latter is deacetylated, ligated with cysteine, and the cysteinyl amino group acetylated by acetyl-CoA to complete the mycothiol biosynthesis pathway. Uptake and concentration of myo-[14C]inositol is rapid in Mycobacterium smegmatis and leads to production of radiolabeled inositol 1-phosphate and mycothiol. This demonstrates the presence of a myo-inositol transporter and a kinase that generates 1L-myo-inositol 1-phosphate. The biochemical pathway of mycothiol biosynthesis is now fully elucidated.
Received for publication, May 17, 2006
, and in revised form, July 25, 2006.
* This work was supported by National Institutes of Health Grant AI49174. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.
The on-line version of this article (available at http://www.jbc.org) contains supplemental data and Figs. S1S3.
1 To whom correspondence should be addressed: Dept. of Chemistry and Biochemistry, University of California at San Diego, La Jolla, CA 92014-0314. Tel.: 858-534-2163; Fax: 858-534-4864; E-mail: rcfahey{at}ucsd.edu.

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Copyright © 2006 by the American Society for Biochemistry and Molecular Biology.
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