class='kwd-title'>Keywords: Sugar nucleotide, Mo'/> Enzymatic synthesis of nucleobase-modified UDP-sugars: scope and limitations
首页> 美国卫生研究院文献>Elsevier Sponsored Documents >Enzymatic synthesis of nucleobase-modified UDP-sugars: scope and limitations
【2h】

Enzymatic synthesis of nucleobase-modified UDP-sugars: scope and limitations

机译:核碱基修饰的UDP糖的酶促合成:范围和局限性

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

class="kwd-title">Keywords: Sugar nucleotide, Modified nucleobase, Enzymatic synthesis, Pyrophosphatase, Epimerase class="head no_bottom_margin" id="idm140660449597904title">AbstractGlucose-1-phosphate uridylyltransferase in conjunction with UDP-glucose pyrophosphorylase was found to catalyse the conversion of a range of 5-substituted UTP derivatives into the corresponding UDP-galactose derivatives in poor yield. Notably the 5-iodo derivative was not converted to UDP-sugar. In contrast, UDP-glucose pyrophosphorylase in conjunction with inorganic pyrophosphatase was particularly effective at converting 5-substituted UTP derivatives, including the iodo compound, into a range of gluco-configured 5-substituted UDP-sugar derivatives in good yields. Attempts to effect 4″-epimerization of these 5-substituted UDP-glucose with UDP-glucose 4″-epimerase from yeast were unsuccessful, while use of the corresponding enzyme from Erwinia amylovora resulted in efficient epimerization of only 5-iodo-UDP-Glc, but not the corresponding 5-aryl derivatives, to give 5-iodo-UDP-Gal. Given the established potential for Pd-mediated cross-coupling of 5-iodo-UDP-sugars, this provides convenient access to the galacto-configured 5-substituted-UDP-sugars from gluco-configured substrates and 5-iodo-UTP.
机译:<!-fig ft0-> <!-fig @ position =“ anchor” mode =文章f4-> <!-fig mode =“ anchred” f5-> <!-fig / graphic | fig / alternatives / graphic mode =“ anchored” m1-> class =“ kwd-title”>关键字:糖核苷酸,修饰的核碱基,酶促合成,焦磷酸酶,差向异构酶 class =“ head no_bottom_margin” id =“ idm140660449597904title”>摘要发现葡萄糖-1-磷酸尿嘧啶转移酶与UDP-葡萄糖焦磷酸化酶结合可催化一系列5-取代的UTP衍生物转化为相应的UDP-半乳糖衍生物,收率不佳。值得注意的是,5-碘衍生物没有被转化为UDP-糖。相反,UDP-葡萄糖焦磷酸化酶与无机焦磷酸酶的结合特别有效地以良好的产率将包括碘化合物在内的5-取代的UTP衍生物转化为一系列葡萄糖-构型的5-取代的UDP-糖衍生物。尝试用来自酵母的UDP-葡萄糖4''-表异构酶对这些5-取代的UDP-葡萄糖进行4''-表异构化是不成功的,而使用来自淀粉欧文氏菌的相应酶只能有效地差向异构化5-碘-UDP-Glc ,而不是相应的5-芳基衍生物,得到5-碘-UDP-Gal。鉴于Pd介导的5-碘-UDP糖之间的交叉偶联已建立潜力,这提供了从葡萄糖配置的底物和5-碘-UTP到半乳糖配置的5-取代-UDP糖的便捷通道。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号