Faculty of Bioresource Sciences, Akita Prefectural University, Akita City, Akita 010-0195, Japan.
Z Naturforsch C J Biosci. 2010 Mar-Apr;65(3-4):257-65. doi: 10.1515/znc-2010-3-414.
The caffeine biosynthetic pathway is composed of three methylation steps, and N-methyltransferase catalyzing each step has high substrate specificity. Since the amino acid sequences among coffee 7-methylxanthosine synthase (CmXRS1), theobromine synthase, and caffeine synthase are highly homologous to each other, these substrate specificities seem to be determined in a very restricted region. The analysis of site-directed mutants for CmXRS1 that naturally acts at the initial step, i.e., 7-N methylation of xanthosine, revealed that the activity of 3-N methylation needs a histidine residue at corresponding position 161 in the CmXRS1 sequence. We succeeded in producing the mutant enzyme which can catalyze the first and second methylation steps in caffeine biosynthesis.
咖啡因生物合成途径由三个甲基化步骤组成,催化每个步骤的 N-甲基转移酶具有很高的底物特异性。由于咖啡 7-甲基黄嘌呤合酶(CmXRS1)、可可碱合酶和咖啡因合酶的氨基酸序列彼此高度同源,这些底物特异性似乎在一个非常有限的区域内确定。对自然作用于初始步骤,即黄嘌呤 7-N 甲基化的 CmXRS1 的定点突变体的分析表明,3-N 甲基化的活性需要 CmXRS1 序列中对应位置 161 的组氨酸残基。我们成功地生产了能够催化咖啡因生物合成中第一和第二甲基化步骤的突变酶。