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Highly efficient preparation of sphingoid bases from glucosylceramides by chemoenzymatic method

机译:化学酶法从葡糖神经酰胺高效制备鞘氨醇碱基

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摘要

Sphingoid base derivatives have attracted increasing attention as promising chemotherapeutic candidates against lifestyle diseases such as diabetes and cancer. Natural sphingoid bases can be a potential resource instead of those derived by time-consuming total organic synthesis. In particular, glucosylceramides (GlcCers) in food plants are enriched sources of sphingoid bases, differing from those of animals. Several chemical methodologies to transform GlcCers to sphingoid bases have already investigated; however, these conventional methods using acid or alkaline hydrolysis are not efficient due to poor reaction yield, producing complex by-products and resulting in separation problems. In this study, an extremely efficient and practical chemoenzymatic transformation method has been developed using microwave-enhanced butanolysis of GlcCers and a large amount of readily available almond β-glucosidase for its deglycosylation reaction of lysoGlcCers. The method is superior to conventional acid/base hydrolysis methods in its rapidity and its reaction cleanness (no isomerization, no rearrangement) with excellent overall yield.
机译:鞘氨醇碱衍生物作为针对生活方式疾病例如糖尿病和癌症的有希望的化学治疗候选物已引起越来越多的关注。天然的类鞘氨醇碱可能是潜在的资源,而不是通过费时的总有机合成而衍生的那些。尤其是,食用植物中的葡糖神经酰胺(GlcCers)是类鞘氨醇碱基的丰富来源,不同于动物。已经研究了几种将GlcCers转化为鞘氨醇碱基的化学方法。然而,这些使用酸或碱水解的常规方法由于反应产率差,产生复杂的副产物并导致分离问题而效率不高。在这项研究中,已经开发出一种极其有效和实用的化学酶转化方法,该方法利用微波增强的GlcCers丁酸酯分解反应和大量易于获得的杏仁β-葡萄糖苷酶用于lysoGlcCers的去糖基化反应。该方法的快速性和反应清洁度(无异构化,无重排)优于常规酸/碱水解方法,且总收率优异。

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