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Substrate Specificity, Kinetic Properties and Inhibition by Fumonisin B1 of Ceramide Synthase Isoforms from Arabidopsis.

Biochem J.. 2016-03; 
KD Luttgeharm, EB Cahoon, JE Markham.
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Codon Optimization ... otherwise noted. Heterologous expression of LOH genes in Saccharomyces cerevisiae - Synthetic, codon optimized, gene constructs were custom synthesized (Genscript, Piscataway, NJ) for each LOH gene. Constructs consisted ... Get A Quote

摘要

Ceramide makes up the acyl-backbone of sphingolipids and plays a central role in determining the function of these essential membrane lipids. In Arabidopsis, the varied chemical composition of ceramide is determined by the specificity of three different isoforms of ceramide synthase, denoted LAG one homologue 1, -2 and -3 (LOH1, LOH2 and LOH3), for a range of long-chain base (LCB) and acyl-CoA substrates. The contribution of each of these isoforms to the synthesis of ceramide was investigated by in vitro ceramide synthase assays. The plant LCB phytosphingosine was efficiently used by the LOH1 and LOH3 isoforms, with LOH1 having the lowest Km for the LCB substrate of the three isoforms. In contrast, sphinganine... More

关键词

Arabidopsis thaliana; ceramide; enzyme kinetics; plant biochemistry; sphingolipid