Department of Chemistry, Texas A&M University, College Station, Texas 77843, USA.
J Am Chem Soc. 2011 Jun 22;133(24):9311-9. doi: 10.1021/ja1110514. Epub 2011 May 26.
In many bacteria tenI is found clustered with genes involved in thiamin thiazole biosynthesis. However, while TenI shows high sequence similarity with thiamin phosphate synthase, the purified protein has no thiamin phosphate synthase activity, and the role of this enzyme in thiamin biosynthesis remains unknown. In this contribution, we identify the function of TenI as a thiazole tautomerase, describe the structure of the enzyme complexed with its reaction product, identify the substrates phosphate and histidine 122 as the acid/base residues involved in catalysis, and propose a mechanism for the reaction. The identification of the function of TenI completes the identification of all of the enzymes needed for thiamin biosynthesis by the major bacterial pathway.
在许多细菌中,tenI 与参与硫胺素噻唑生物合成的基因簇在一起。然而,尽管 TenI 与硫胺素磷酸合酶具有很高的序列相似性,但纯化的蛋白没有硫胺素磷酸合酶活性,该酶在硫胺素生物合成中的作用仍然未知。在本研究中,我们确定了 TenI 的功能是硫唑式互变异构酶,描述了酶与反应产物结合的结构,确定了磷酸和组氨酸 122 作为催化涉及的酸碱残基,并提出了反应机制。TenI 功能的确定完成了主要细菌途径中所有硫胺素生物合成所需酶的鉴定。