Aoki Koichiro, Mutaguchi Yuta, Hemmi Hisashi, Yoshimura Tohru, Ito Tomokazu
Department of Applied Biosciences, Graduate School of Bioagricultural Sciences, Nagoya University, Furou-chou, Chikusa, Nagoya, Aichi, 464-8601, Japan.
Department of Biotechnology, Faculty of Bioresource Sciences, Akita Prefectural University, Akita, Japan.
Chembiochem. 2025 Mar 15;26(6):e202401075. doi: 10.1002/cbic.202401075. Epub 2025 Feb 27.
Various lactic acid bacteria synthesize d-branched-chain amino acids (d-BCAA) during growth, but their physiological function remains largely elusive. The pyridoxal phosphate-dependent enzyme isoleucine 2-epimerase (ILEP) has been identified as the key enzyme responsible for d-BCAA biosynthesis. Comparative genomic analyses revealed that genes encoding ILEP and an uncharacterized amino acid-polyamine-organocation (APC) family transporter are adjacent in several d-BCAA-producing bacteria, suggesting a functional link between these two proteins in d-BCAA metabolism. In this study, we investigated the function of the APC family transporter from Lactobacillus fermentum (LfAAP). Using heterologous expression systems in Escherichia coli and Lactococcus lactis, we demonstrated that LfAAP functions as a non-stereospecific BCAA importer. Mutational analysis revealed that Ala119 and Met331 play critical roles in substrate recognition. Heterologous expression of LfAAP and/or LfILEP in a L. lactis strain, which lacks the ILEP-AAP genes operon, revealed that ILEP functions as both synthetic and catabolic enzyme for d-BCAA. Our findings suggest that the ILEP-AAP system contribute to storage and subsequent utilization of BCAA in a form that is less accessible by other organisms, providing a potential competitive advantage in microbial environments.
多种乳酸菌在生长过程中会合成d-支链氨基酸(d-BCAA),但其生理功能在很大程度上仍不清楚。磷酸吡哆醛依赖性酶异亮氨酸2-表异构酶(ILEP)已被确定为负责d-BCAA生物合成的关键酶。比较基因组分析表明,在几种产生d-BCAA的细菌中,编码ILEP的基因和一个未表征的氨基酸-多胺-有机阳离子(APC)家族转运蛋白的基因相邻,这表明这两种蛋白质在d-BCAA代谢中存在功能联系。在本研究中,我们研究了发酵乳杆菌(LfAAP)中APC家族转运蛋白的功能。利用大肠杆菌和乳酸乳球菌中的异源表达系统,我们证明LfAAP作为一种非立体特异性的BCAA转运蛋白发挥作用。突变分析表明,Ala119和Met331在底物识别中起关键作用。在缺乏ILEP-AAP基因操纵子的乳酸乳球菌菌株中异源表达LfAAP和/或LfILEP,结果表明ILEP作为d-BCAA的合成酶和分解代谢酶发挥作用。我们的研究结果表明,ILEP-AAP系统有助于以其他生物体难以获取的形式储存和随后利用BCAA,在微生物环境中提供了潜在的竞争优势。