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Evidence of a novel mevalonate pathway in archaea.

Biochemistry (2014-06-11)
Jeffrey M Vinokur, Tyler P Korman, Zheng Cao, James U Bowie
ABSTRAKT

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.

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Sigma-Aldrich
(RS)-Mevalonic acid lithium salt, ≥96.0% (GC)
Sigma-Aldrich
Leucine Enkephalin acetate salt hydrate, ≥95% (HPLC)
Supelco
(RS)-Mevalonic acid lithium salt, analytical standard
Leucine, European Pharmacopoeia (EP) Reference Standard
Sigma-Aldrich
DL-Leucine, ≥99% (HPLC)