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古菌中新型甲羟戊酸途径的证据。

Evidence of a novel mevalonate pathway in archaea.

机构信息

Department of Chemistry and Biochemistry, UCLA-DOE Institute for Genomics and Proteomics, Molecular Biology Institute, University of California at Los Angeles , Los Angeles, California 90095-1570, United States.

出版信息

Biochemistry. 2014 Jul 1;53(25):4161-8. doi: 10.1021/bi500566q. Epub 2014 Jun 18.

Abstract

Isoprenoids make up a remarkably diverse class of more than 25000 biomolecules that include familiar compounds such as cholesterol, chlorophyll, vitamin A, ubiquinone, and natural rubber. The two essential building blocks of all isoprenoids, isopentenyl pyrophosphate (IPP) and dimethylallyl pyrophosphate (DMAPP), are ubiquitous in the three domains of life. In most eukaryotes and archaea, IPP and DMAPP are generated through the mevalonate pathway. We have identified two novel enzymes, mevalonate-3-kinase and mevalonate-3-phosphate-5-kinase from Thermoplasma acidophilum, which act sequentially in a putative alternate mevalonate pathway. We propose that a yet unidentified ATP-independent decarboxylase acts upon mevalonate 3,5-bisphosphate, yielding isopentenyl phosphate, which is subsequently phosphorylated by the known isopentenyl phosphate kinase from T. acidophilum to generate the universal isoprenoid precursor, IPP.

摘要

异戊二烯类化合物由 25000 多种生物分子组成,种类繁多,包括胆固醇、叶绿素、维生素 A、泛醌和天然橡胶等常见化合物。所有异戊二烯类化合物的两个必需结构单元,异戊烯焦磷酸(IPP)和二甲基烯丙基焦磷酸(DMAPP),在生命的三个领域中无处不在。在大多数真核生物和古菌中,IPP 和 DMAPP 是通过甲羟戊酸途径生成的。我们从嗜酸热原体中鉴定出两种新的酶,甲羟戊酸激酶和甲羟戊酸 3-磷酸-5-激酶,它们在假定的替代甲羟戊酸途径中依次作用。我们提出,一种尚未鉴定的非依赖于 ATP 的脱羧酶作用于甲羟戊酸 3,5-二磷酸,生成异戊烯磷酸,然后被已知的嗜酸热原体异戊烯磷酸激酶磷酸化,生成通用的异戊二烯前体 IPP。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/33ef/4081127/907d9be8b109/bi-2014-00566q_0002.jpg

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