Hyaluronidases improve the hyaluronic acid yield during the fermentation of Streptococcus zooepidemicus.

Authors

Chuan-Li Kang, De-Qiang Zheng, Zhi-Yuan Yao, Kang Yang, Yuxue Zhao, Zihan Mao, Yang Liu, Haijun Li, Jin-Song Gong, Lei Liu, Qingwen Jia, Zheng-Hong Xu, Jin-Song Shi, Le Xue

Published in

Frontiers in bioengineering and biotechnology. Volume 13. Pages 1625009. Epub Jul 16, 2025.

Abstract

Hyaluronic acid (HA), a linear acidic mucopolysaccharide with exceptional biocompatibility, is extensively utilized in pharmaceuticals and cosmetics. Industrial HA production predominantly relies on Streptococcus zooepidemicus fermentation. However, the accumulation of high-molecular-weight (HMW) HA increases broth viscosity, impeding nutrient diffusion and limiting yield.
To address this, four HAases, HHya1, LHya2, SHya3, and EHya4, were expressed and screened for enzymatic activity. we evaluated the strategic addition of hyaluronidases (HAases) to degrade HMW HA during fermentation, thereby reducing viscosity and enhancing productivity.
HHya1 and EHya4 exhibited superior expression levels and catalytic efficiency. Purification and functional characterization revealed distinct degradation profiles, HHya1 hydrolyzed HMW HA into saturated tetrasaccharides, while EHya4 generated unsaturated disaccharides. In shake-flask fermentations, supplementation with 1500 U/L EHya4 increased HA titer by 12%, outperforming HHya1. Scaling to bioreactor cultivation with viscosity-controlled HAase dosing further optimized productivity. By administering HAase at intervals corresponding to viscosity thresholds, HA titers reached 10.3 g/L, representing a 14.4% increase over baseline.
These findings demonstrate that HAase application alleviates viscosity-associated bottlenecks in S. zooepidemicus fermentations, establishing an optimized process for scalable HA production. This approach balances enzymatic degradation with microbial growth kinetics, offering a practical strategy for industrial HA biosynthesis.

PMID:
40741534
Bibliographic data and abstract were imported from PubMed on 31 Jul 2025.

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