Dunn Michael F, Niks Dimitri, Ngo Huu, Barends Thomas R M, Schlichting Ilme
Department of Biochemistry, University of California, Riverside, CA 92521, USA.
Trends Biochem Sci. 2008 Jun;33(6):254-64. doi: 10.1016/j.tibs.2008.04.008. Epub 2008 May 15.
Substrate channeling between enzymes has an important role in cellular metabolism by compartmentalizing cytoplasmic synthetic processes. The bacterial tryptophan synthases are multienzyme nanomachines that catalyze the last two steps in L-tryptophan biosynthesis. The common metabolite indole is transferred from one enzyme to the other in each alphabeta-dimeric unit of the alpha2beta2 complex via an interconnecting 25-A-long tunnel. Recent solution studies of the Salmonella typhimurium alpha2beta2 complex coupled with X-ray crystal-structure determinations of complexes with substrates, intermediates and substrate analogs have driven important breakthroughs concerning the identification of the linkages between the bi-enzyme complex structure, catalysis at the alpha- and beta-active sites, and the allosteric regulation of substrate channeling.
通过对细胞质合成过程进行区室化,酶之间的底物通道化在细胞代谢中起着重要作用。细菌色氨酸合酶是多酶纳米机器,催化L-色氨酸生物合成的最后两步。在α2β2复合物的每个αβ二聚体单元中,常见代谢物吲哚通过一条25埃长的互连隧道从一种酶转移到另一种酶。最近对鼠伤寒沙门氏菌α2β2复合物的溶液研究,以及结合底物、中间体和底物类似物的复合物的X射线晶体结构测定,在双酶复合物结构、α和β活性位点的催化以及底物通道化的变构调节之间的联系识别方面取得了重要突破。