Abstract
INTRODUCTION: 5-Aminolevulinic acid (5-ALA) is a nonprotein amino acid with broad applications in agriculture, medicine, and the food industry. In recent years, substantial efforts have been devoted to enhancing its biosynthesis. The catalytic activity of 5-aminolevulinic acid synthase (ALAS) is a critical determinant of production efficiency. METHODS: In this study, a growth-coupled selection strategy was developed to improve ALAS from Rhodobacter capsulatus SB1003 using random and site-specific mutagenesis. The derived ALAS mutant was then introduced into the GRAS-certified producer Corynebacterium glutamicum, followed by fermentation optimization. RESULTS: The enzymatic activity of the best mutant, D4,7,18, increased by 67.41%, leading to 1.18-fold higher 5-ALA accumulation than that of the wild type. Enzymatic analysis suggested that the enhanced activity of D4,7,18 was partly attributable to stronger PLP binding and a lower K (m) for glycine. During fermentation optimization, the results underscored the crucial roles of dissolved oxygen, Fe(2+) and glycine supplementation. Ultimately, 8.72 g/L of 5-ALA was produced within 60 h, with minimal accumulation of organic acid byproducts. CONCLUSION: The growth-coupled selection strategy demonstrated in this study offers a promising approach for optimizing other enzymes and metabolic pathways, provided that an appropriate selection strain and screening conditions are employed.