Assimilation of Xylose, Mannose, and Mannitol for Synthesis of Glucuronoxylomannan of Cryptococcus neoformans Determined by 13 C Nuclear Magnetic Resonance Spectroscopy

• Published in: Infection and immunity Vol. 66; no. 6; pp. 2996 - 2998
• Main Authors: Cherniak, Robert, O’Neill, Eric B., Sheng, Shuqun
• Format: Journal Article
• Language: English
• Published: 01.06.1998
• ISSN: 0019-9567; 1098-5522
• DOI: 10.1128/IAI.66.6.2996-2998.1998

ABSTRACT Cryptococcus neoformans NIH 409 was cultured in a defined medium containing d -[1- 13 C]xylose (Xyl), d -[1- 13 C]mannose (Man), or d -[1- 13 C]mannitol as the sole carbon source. The distribution of 13 C in the Man, Xyl, glucuronic acid (GlcA), and O-acetyl constituents of native and de-O-acetylated glucuronoxylomannan (GXM) was determined by one-dimensional 13 C nuclear magnetic resonance spectroscopy. The carbon chain of Man was incorporated intact into GXM since 13 C was observed only in carbon 1 of Man, GlcA, and Xyl. The carbon chain of mannitol was incorporated intact into GXM since 13 C 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.