Identification of the missing links in prokaryotic pentose oxidation pathways - Evidence for enzyme recruitment
2006 (English)In: Journal of Biological Chemistry, ISSN 0021-9258, E-ISSN 1083-351X, Vol. 281, no 37, 27378-27388 p.Article in journal (Refereed) Published
The pentose metabolism of Archaea is largely unknown. Here, we have employed an integrated genomics approach including DNA microarray and proteomics analyses to elucidate the catabolic pathway for D-arabinose in Sulfolobus solfataricus. During growth on this sugar, a small set of genes appeared to be differentially expressed compared with growth on D-glucose. These genes were heterologously overexpressed in Escherichia coli, and the recombinant proteins were purified and biochemically studied. This showed that D-arabinose is oxidized to 2-oxoglutarate by the consecutive action of a number of previously uncharacterized enzymes, including a D-arabinose dehydrogenase, a D-arabinonate dehydratase, a novel 2-keto-3-deoxy-D-arabinonate dehydratase, and a 2,5-dioxopentanoate dehydrogenase. Promoter analysis of these genes revealed a palindromic sequence upstream of the TATA box, which is likely to be involved in their concerted transcriptional control. Integration of the obtained biochemical data with genomic context analysis strongly suggests the occurrence of pentose oxidation pathways in both Archaea and Bacteria, and predicts the involvement of additional enzyme components. Moreover, it revealed striking genetic similarities between the catabolic pathways for pentoses, hexaric acids, and hydroxyproline degradation, which support the theory of metabolic pathway genesis by enzyme recruitment.
Place, publisher, year, edition, pages
2006. Vol. 281, no 37, 27378-27388 p.
l-arabinose metabolism, archaeon sulfolobus-solfataricus, entner-doudoroff pathway, escherichia-coli, crystal-structure, thermoacidophilic crenarchaeon, fumarylacetoacetate hydrolase, pseudomonas-saccharophila, glutamate-dehydrogenase, caulobacter-crescentus
Biochemistry and Molecular Biology
IdentifiersURN: urn:nbn:se:kth:diva-15980DOI: 10.1074/jbc.M605549200ISI: 000240397700064ScopusID: 2-s2.0-33748754005OAI: oai:DiVA.org:kth-15980DiVA: diva2:334022
QC 20100525 201202242010-08-052010-08-052012-02-24Bibliographically approved