Kurnasov Oleg, Goral Vasiliy, Colabroy Keri, Gerdes Svetlana, Anantha Shubha, Osterman Andrei, Begley Tadhg P
Integrated Genomics, 2201 West Campbell Park Drive, Chicago, IL 60612, USA.
Chem Biol. 2003 Dec;10(12):1195-204. doi: 10.1016/j.chembiol.2003.11.011.
Previous studies have demonstrated two different biosynthetic pathways to quinolinate, the universal de novo precursor to the pyridine ring of NAD. In prokaryotes, quinolinate is formed from aspartate and dihydroxyacetone phosphate; in eukaryotes, it is formed from tryptophan. It has been generally believed that the tryptophan to quinolinic acid biosynthetic pathway is unique to eukaryotes; however, this paper describes the use of comparative genome analysis to identify likely candidates for all five genes involved in the tryptophan to quinolinic acid pathway in several bacteria. Representative examples of each of these genes were overexpressed, and the predicted functions are confirmed in each case using unambiguous biochemical assays.
先前的研究已经证明了喹啉酸有两种不同的生物合成途径,喹啉酸是NAD吡啶环的通用从头合成前体。在原核生物中,喹啉酸由天冬氨酸和磷酸二羟丙酮形成;在真核生物中,它由色氨酸形成。人们普遍认为色氨酸到喹啉酸的生物合成途径是真核生物所特有的;然而,本文描述了利用比较基因组分析来确定几种细菌中色氨酸到喹啉酸途径中涉及的所有五个基因的可能候选基因。这些基因中的每一个的代表性例子都被过表达,并在每种情况下使用明确的生化分析来证实预测的功能。