Assimilation of xylose, mannose, and mannitol for synthesis of glucuronoxylomannan of Cryptococcus neoformans determined by 13C nuclear magnetic resonance spectroscopy

Cryptococcus neoformans NIH 409 was cultured in a defined medium containing D-[1-13C]xylose (Xyl), D-[1-13C]mannose (Man), or D-[1-13C]mannitol as the sole carbon source. The distribution of 13C in the Man, Xyl, glucuronic acid (GlcA), and O-acetyl constituents of native and de-O-acetylated glucuron...

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Published inInfection and immunity Vol. 66; no. 6; pp. 2996 - 2998
Main Authors CHERNIAK, R, O'NEILL, E. B, SHUQUN SHENG
Format Journal Article
LanguageEnglish
Published Washington, DC American Society for Microbiology 01.06.1998
SeriesNote
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Summary:Cryptococcus neoformans NIH 409 was cultured in a defined medium containing D-[1-13C]xylose (Xyl), D-[1-13C]mannose (Man), or D-[1-13C]mannitol as the sole carbon source. The distribution of 13C in the Man, Xyl, glucuronic acid (GlcA), and O-acetyl constituents of native and de-O-acetylated glucuronoxylomannan (GXM) was determined by one-dimensional 13C nuclear magnetic resonance spectroscopy. The carbon chain of Man was incorporated intact into GXM since 13C was observed only in carbon 1 of Man, GlcA, and Xyl. The carbon chain of mannitol was incorporated intact into GXM since 13C was observed only in carbons 1 and 6. This was expected since mannitol has an axis of symmetry. The carbon chain of Xyl was identified only in carbons 1 and 3 of Man, GlcA, and Xyl. This pattern of labeling is consistent with the assimilation of Xyl through the pentophosphate pathway.
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Corresponding author. Mailing address: Department of Chemistry, Georgia State University, University Plaza, Atlanta, GA 30303. Phone: (404) 651-3868. Fax: (404) 651-1416. E-mail: cherniak@gsu.edu.
Editor: T. R. Kozel
Present address: Department of Chemistry, Rutgers University, Piscataway, N.J.
ISSN:0019-9567
1098-5522