Possible Regulation of Trehalose Metabolism by Methylation in Saccharomyces Cerevisiae

Sengupta, Shinjinee and Chadhuri, Paramita and Lahiri, Sagar and Dutta, Trina and Banerjee, Shakri and Majhi, Ramdhan and Ghosh, Anil K (2011) Possible Regulation of Trehalose Metabolism by Methylation in Saccharomyces Cerevisiae. Journal of Cellular Physiology, 226. pp. 158-164. ISSN 0021-9541


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    The current study was undertaken to correlate post-translational protein modification by methylation with the functionality of enzymes involved in trehalose metabolism in Saccharomyces cerevisiae. Trehalose is an economically important disaccharide providing protection against various kinds of stresses. It also acts as a source of cellular energy by storing glucose. Methyl group donor S-adenosyl L-methionine (AdoMet) and methylation inhibitor-oxidized adenosine (AdOx) were used for the methylation study. AdoMet delayed initial growth of the cells but the overall growth rate remained same suggesting its interference in G1 phase of the cell cycle. Metabolic-altered enzyme activities of acid trehalase (AT), neutral trehalase (NT), and trehalose-6-phosphate synthase (TPS) were observed when treated with AdOx and AdoMet separately. A positive effect of methylation was observed in TPS, hence, it was purified in three different conditions, using AdoMet, AdOx, and control. Differences in mobility of methylated, methylation-inhibited, and control TPS during acidic native gel electrophoresis confirmed the occurrence of induced methylation. Hydrolysis under alkaline pH conditions revealed that methylation of TPS was different than O-methylation. MALDI-TOF analysis of trypsin-digested samples of purified methylated, methylation-inhibited, and control TPS revealed that an increase of 18 Da mass in methylated peptides suggesting the introduction of methyl ester in TPS. Results of amino acid analysis corroborated the presence of methyl cysteine. The data presented here strongly suggests that trehalose production was enhanced due to methylation of TPS arising from carboxymethylation of cysteine residues. J. Cell. Physiol. 226: 158–164, 2010. � 2010 Wiley-Liss, Inc.

    Item Type: Article
    URI: http://www.eprints.iicb.res.in/id/eprint/117
    Subjects: Drug Development/Diagnostics & Biotechnology
    Divisions: Indian Institute of Chemical Biology
    Depositing User: Ms Sutapa Ganguly
    Date Deposited: 29 Sep 2011 15:22
    Last Modified: 20 Jan 2012 10:54
    Official URL: http://dx.doi.org/10.1002/jcp.22317

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