期刊文献+

天然烟酰胺辅因子再生体系及其人工类似物研究进展 被引量:4

Advances in regeneration system of natural nicotinamide cofactor and its artificial analogues
下载PDF
导出
摘要 氧化还原酶可以催化具有特定区域选择性、化学选择性、立体选择性的反应,反应条件温和且催化效率高,因此在有机化学和制药领域发挥着日益重要的作用。绝大多数氧化还原酶依赖烟酰胺腺嘌呤二核苷酸NAD(H)和烟酰胺腺嘌呤二核苷酸磷酸NADP(H)为酶促反应提供氧化还原当量。NAD(H)/NADP(H)由于价格昂贵、稳定性差导致无法化学计量投入。经过几十年研究,形成了4种经典的NAD(H)/NADP(H)再生方法:酶法、化学法、电化学法和光化学法,与此同时,一系列稳定性好、活性高且廉价的人工烟酰胺辅因子m NAD(H)s尤其是1,4-二氢吡啶类烟酰胺辅因子的开发和利用为NAD(H)/NADP(H)工业化运用提供了新的思路。 Oxidoreductases have drawn considerable attention as mild and efficient catalysts in the fields of organic synthesis and medical sciences due to they can catalyze regio-, chemo- and stereoselective transformations that cannot be easily achieved by chemical catalysts. Cofactors are required in oxidoreductase-catalyzed reactions, commonly in the form of nicotinamide adenine dinucleotide and nicotinamide adenine dinucleotide phosphate, abbreviated as NAD(H) and NADP(H). Given the high cost and physical instability of NAD(H)/NADP(H), the stoichiometric usage is not practical for industrial applications. After decades, four main strategies such as enzymatic, chemical, electrochemical and photochemical method have been used for the cofactor regeneration. Meanwhile, the development of stable, highly active and inexpensive artificial nicotinamide cofactors particularly 1,4-dihydropyridine derivatives has led to a new breakthrough.
出处 《化工学报》 EI CAS CSCD 北大核心 2018年第1期259-271,共13页 CIESC Journal
基金 国家自然科学基金项目(21776132,21406110,21390204):江苏省自然科学基金项目(BK20140938) “青年人才托举工程”项目.
关键词 生物催化 烟酰胺辅因子 电化学 光化学 人工辅因子 biocatalysis enzyme nicotinamide cofactor electrochemistry photochemistry artificial cofactor
  • 相关文献

参考文献5

二级参考文献257

  • 1[31]Kameda A,Shiba T,Kawazoe Y,et al.Noguchi T A novel ATP regeneration system using polyphosphate-AMP phosphotransferase and polyphosphate kinase[J].J Biosci Bioeng,2001,91:557-563. 被引量:1
  • 2[32]Ichikawa Y,Wang R,Wong CH.Regeneration of sugar nucleotide for enzymatic oligosaccharide synthesis[J].Methods Enzymol,1994,247:107-127. 被引量:1
  • 3[33]Bulter T,Elling L.Enzymatic synthesis of nucleotide sugars[J]. Glycoconj J,1999,16:147-159. 被引量:1
  • 4[34]Endo T,Koizumi S,Tabata K,et al.Large-scale production of CMP-NeuAc and sialylated oligosaccharides through bacterial coupling[J]. Appl Microbiol Biotechnol,2000,53:257-261. 被引量:1
  • 5[35]Tabata K,Koizumi S,Endo T,et al.Production of UDP-Nacetylglucosamine by coupling metabolically engineered bacteria[J]. Biotechnol Lett,2000,22:479-483. 被引量:1
  • 6[36]Tabata K,Koizumi S,Endo T,et al.Production of N-acetyl-D-neuraminic acid by coupling bacteria expressing N-acetyl- D-glucosamine 2-epimerase and N-acetyl-D-neuraminic acid synthetase[J].Enzyme Microb Technol ,2002,30:327-333. 被引量:1
  • 7[37]Lee SG,Lee JO,Yi JK,et al.Production of cytidine 5(-monophosphate N-acetylneuraminic acid using recombinant Escherichia coli as a biocatalyst[J].Biotechnol Bioeng,2002,80:516-524. 被引量:1
  • 8[38]Chen X,Zhang JB,Kowal P,et al.Transferring a biosynthetic cycle into a productive Escherichia coli strain:large-scale synthesis of galactosides[J].J Am Chem Soc,2001,123:8 866-8 867. 被引量:1
  • 9[39]Lin CH,Shen GJ,Garciajunceda E,et al.Enzymatic synthesis and regeneration of 3β-phosphoadenosine 5β-phosphosulfate (PAPS) for regioselective sulfation of oligosaccharides[J].J Am Chem Soc,1995,117:8 031-8 032. 被引量:1
  • 10[40]Burkart MD,Izumi M,Wong CH.Enzymatic regeneration of 3-phosphoadenosine-5-phosphosulfate using aryl sulfotransferase for the preparative enzymatic synthesis of sulfated carbohydrates[J].Angew Chem Int Ed Engl,1999,38:2 747-2 750. 被引量:1

共引文献34

同被引文献13

引证文献4

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部