Identification and Characterization of a Highly Active Hyaluronan Lyase from Enterobacter asburiae

• Published in: Marine drugs 2024-08, Vol.22 (9), p.399
• Main Authors: Zhang, Linjing, Jiang, Jiayu, Liu, Wei, Wang, Lianlong, Yao, Zhiyuan, Li, Heng, Gong, Jinsong, Kang, Chuanli, Liu, Lei, Xu, Zhenghong, Shi, Jinsong
• Format: Article
• Language: English
• Subjects: Amino acids; Annotations; Carbohydrates; Cosmetics; Degradation; Dextrose; Disaccharides; E coli; Enterobacter - enzymology; Enterobacter - genetics; Enterobacter asburiae; Enzymatic activity; Enzyme activity; Enzymes; Escherichia coli; Escherichia coli - genetics; Gene sequencing; Genes; genome; Genomes; Genomic analysis; Glucose; Glycosaminoglycans; hyaluronan lyase; Hyaluronic acid; Hyaluronic Acid - biosynthesis; Hyaluronic Acid - metabolism; hyaluronic acid oligosaccharides; Hydrogen-Ion Concentration; Industrial wastes; Industrial wastewater; Metabolism; Microorganisms; Molecular weight; Oligosaccharides; Phylogenetics; Polysaccharide-Lyases - genetics; Polysaccharide-Lyases - metabolism; Polysaccharides; Sugars; Wastewater; Whole Genome Sequencing
• ISSN: 1660-3397; 1660-3397
• DOI: 10.3390/md22090399

Hyaluronic acid (HA) is a well-known functional marine polysaccharide. The utilization and derivative development of HA are of great interest. Hyaluronan lyase has wide application prospects in the production of HA oligosaccharides and lower molecular weight HA. In this study, a strain of CGJ001 with high hyaluronan lyase activity was screened from industrial wastewater. This strain exhibited an impressive enzyme activity of 40,576 U/mL after being incubated for 14 h. Whole genome sequencing analysis revealed that CGJ001 contained a cluster of genes involved in HA degradation, transport, and metabolism. A newly identified enzyme responsible for glycosaminoglycan degradation was designated as HylEP0006. A strain of BL21(DE3)/ ET-22b(+) was successfully constructed. HylEP0006 exhibited optimal degradation at 40 °C and pH 7.0, showing a high activity of 950,168.3 U/mg. HylEP0006 showed specific activity against HA. The minimum degradation fragment of HylEP0006 was hyaluronan tetrasaccharides, and HylEP0006 could efficiently degrade HA into unsaturated disaccharides (HA2), with HA2 as the final product. These characteristics indicate that HylEP0006 has a potential application prospect for the extraction and utilization of hyaluronic acid.