期刊文献+

法呢基焦磷酸(FPP)的生物合成及其分子调控 被引量:14

The Biosynthetic Pathway and Molecular Regulation of Farnesyl Diphosphate(FPP)
下载PDF
导出
摘要 法呢基焦磷酸合酶作为异戊二烯途径中的重要调节酶,是许多萜类物质的合成前体。FPS的cDNA克隆在许多生物体中也已得到了分离并进行了表达特性研究。从FPP的生物合成途径入手,对FPP生物学特性、FPS酶基因调控的相关信息进行了综述,同时对FPS在基因工程方面的应用进行了展望。 In the isoprenoid biosynthesis pathway,famesyl diphosphate synthase (FPS,EC2. 5. 1. 1/EC2. 5. 1. 10) catalyzes two consecutive condensations of isopentenyl diphosphate with dimethylallyl diphosphate,forming geranyl diphosphate (FPP)which is a common precursor for the biosynthesis of sterols,dolichols,mitochondrial electron transfer chain components,prenylated proteins and a wide range of secondary sesquiterpenoids. Recently,cDNAs encoding FPS had been isolated from a number of plant species. In the paper,the biosythasis pathway and molecular regulation of farnesyl diphosphate were reviewed,and progress of FPS applied in genetic engineering was also prospected.
出处 《生物技术通报》 CAS CSCD 2007年第2期67-71,共5页 Biotechnology Bulletin
关键词 法呢基焦磷酸 生物学功能 分子调控 Farnesyl diphosphate Biological function Molecular regulation
  • 相关文献

参考文献4

二级参考文献53

  • 1Luckman SP,Coxon FP,Ebetino FH,et al.Heterocycle-containing bisphosphonates cause apoptosis and inhibit bone resorption by preventing protein prenylation:evidence from structure-activity relationships in J774 macrophages[J].J Bone Miner Res,1998,13(11):16
  • 2Dunford JE,Thompson K,Coxon FP,et al.Relationships for inhibition offarnesyl diphosphonate synthase in vitro and inhibition of bone resorption in vivo by nitrogen-containing bisphosphonates[J].J Pharm Exp Ther,2001,296(2):235-242.
  • 3Kotsikorou E,Oldfield E.A quantitative structure-activity relationship and pharmacophore modeling investigation of aryl-X and heterocyclic bisphosphonates as bone resorption agents[J].J Med Chem,2003,46(14):2932-2944.
  • 4Benford HL,Frith JC,Auriola S,et al.Farnesol and geranylgeraniol prevent activation of caspases by aminobisphosphonates:biochemical evidence for twodistinct pharmacological classes of bisphosphonate drugs[J].Mol Pharmacol,1999,56(1):131-140.
  • 5Auriola S,Frith J,Rogers MJ,et al.Identification of adenine nucleotide-containing metabolites of bisphosphonate drugs using ion-pair liquid chromatography-electrospray mass spectrometry[J].J Chrom:B,1997,704(1-2):187-195.
  • 6Frith JC,Monkkonen J,Blackburn GM,et al.Clodronate and liposome-encapsulated clodronate are metabolized to a toxic ATP analogue,adenosine 5′-(beta,gamma-dichloromethylene)triphosphate,by mammalian cells in vitro[J].J Bone Miner Res,1997,12(9):1358-1367.
  • 7Lehenkari PP,Kellinsalmi M,Napankangas JP,et al.Further insight intomechanism of action of clodronate:inhibition of mitochondrial ADP/ATP translocase by a nonhydrolyzable,adenine-containing metabolite[J].Mol Pharmacol,2002,61(5):1255-1262.
  • 8Luckman SP,Hughes DE,Coxon FP,et al.Nitrogen-containing bisphosphonates inhibit the mevalonate pathway and prevent post-translational prenylation of GTP-binding proteins,including Ras[J].J Bone Miner Res,1998,13(4):581-589.
  • 9Fisher JE,Rogers MJ,Halasy JM,et al.Alendronate mechanism of action:geranylgeraniol,an intermediate in the mevalonate pathway,prevents inhibition ofosteoclast formation,bone resorption and kinase activation in vitro[J].Proc Natl Acad Sci,1999,96(1):133-13
  • 10Van Beek E,Lowik,van der Pluijm G,et al.The role of geranylgeranylation in bone resorption and its suppression by bisphosphonates in fetal bone explants in vitro:a clue to the mechanism of action of nitrogen-containing bisphosphonates[J].J Bone Miner Res,

共引文献58

同被引文献205

引证文献14

二级引证文献75

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