Department of Applied Chemistry, Faculty of Science and Engineering, Waseda University, Shinjuku-ku, Tokyo, Japan.
Appl Environ Microbiol. 2013 Aug;79(16):5023-9. doi: 10.1128/AEM.01003-13. Epub 2013 Jun 14.
Functional peptides are expected to be beneficial compounds that improve our quality of life. To address the growing need for functional peptides, we have examined peptide synthesis by using microbial enzymes. l-Amino acid ligase (Lal) catalyzes the condensation of unprotected amino acids in an ATP-dependent manner and is applicable to fermentative production. Hence, Lal is a promising enzyme to achieve cost-effective synthesis. To obtain a Lal with novel substrate specificity, we focused on the putative Lal involved in the biosynthesis of the dipeptidic phytotoxin designated tabtoxin. The tabS gene was cloned from Pseudomonas syringae NBRC14081 and overexpressed in Escherichia coli cells. The recombinant TabS protein produced showed the broadest substrate specificity of any known Lal; it detected 136 of 231 combinations of amino acid substrates when dipeptide synthesis was examined. In addition, some new substrate specificities were identified and unusual amino acids, e.g., l-pipecolic acid, hydroxy-l-proline, and β-alanine, were found to be acceptable substrates. Furthermore, kinetic analysis and monitoring of the reactions over a short time revealed that TabS showed distinct substrate selectivity at the N and C termini, which made it possible to specifically synthesize a peptide without by-products such as homopeptides and heteropeptides with the reverse sequence. TabS specifically synthesized the following functional peptides, including their precursors: l-arginyl-l-phenylalanine (antihypertensive effect; yield, 62%), l-leucyl-l-isoleucine (antidepressive effect; yield, 77%), l-glutaminyl-l-tryptophan (precursor of l-glutamyl-l-tryptophan, which has antiangiogenic activity; yield, 54%), l-leucyl-l-serine (enhances saltiness; yield, 83%), and l-glutaminyl-l-threonine (precursor of l-glutamyl-l-threonine, which enhances saltiness; yield, 96%). Furthermore, our results also provide new insights into tabtoxin biosynthesis.
功能肽有望成为改善我们生活质量的有益化合物。为了满足对功能肽日益增长的需求,我们研究了利用微生物酶进行肽合成。L-氨基酸连接酶(Lal)以 ATP 依赖性方式催化未保护氨基酸的缩合,适用于发酵生产。因此,Lal 是一种很有前途的实现成本效益合成的酶。为了获得具有新型底物特异性的 Lal,我们专注于参与二肽植物毒素命名为 tabtoxin 生物合成的假定 Lal。tabS 基因从 Pseudomonas syringae NBRC14081 中克隆,并在大肠杆菌细胞中过表达。产生的重组 TabS 蛋白显示出任何已知 Lal 中最广泛的底物特异性;当检查二肽合成时,它检测到 231 种氨基酸底物组合中的 136 种。此外,还确定了一些新的底物特异性,并且发现了一些不寻常的氨基酸,例如 l-哌啶酸、羟基-l-脯氨酸和 β-丙氨酸,它们是可接受的底物。此外,动力学分析和短时间内的反应监测表明,TabS 在 N 和 C 末端表现出明显的底物选择性,这使得可以特异性合成没有副产物(如具有反向序列的同肽和异肽)的肽。TabS 特异性合成了以下功能肽,包括它们的前体:l-精氨酰-l-苯丙氨酸(降血压作用;产率 62%)、l-亮氨酰-l-异亮氨酸(抗抑郁作用;产率 77%)、l-谷氨酰-l-色氨酸(具有抗血管生成活性的 l-谷氨酰-l-色氨酸前体;产率 54%)、l-亮氨酰-l-丝氨酸(增强咸味;产率 83%)和 l-谷氨酰-l-苏氨酸(增强咸味的 l-谷氨酰-l-苏氨酸前体;产率 96%)。此外,我们的结果还为 tabtoxin 生物合成提供了新的见解。