4.7 Article

Biosynthesis of non-sulfated high-molecular-weight glycosaminoglycans and specific-sized oligosaccharides

Journal

CARBOHYDRATE POLYMERS
Volume 295, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.carbpol.2022.119829

Keywords

Glycosaminoglycans; Chondroitin; Hyaluronan; Heparosan; Molecular weight; Disaccharide; Tetrasaccharide

Funding

  1. National Key Research and Development Program of China [2021YFC2103100]
  2. Jiangsu Province Natural Science Fund for Distinguished Young Scholars [BK20200025]
  3. National Natural Science Foundation of China [32000058]
  4. Key Technologies R & D Program of Jiangsu Province [BE2019630]

Ask authors/readers for more resources

A membrane shield strategy was developed to produce high-molecular-weight glycosaminoglycans by recruiting type II NSGAG synthases in Corynebacterium glutamicum, while a synchronized depolymerization-polymerization strategy was developed by coexpressing NSGAGs synthases and lyases for specific size oligosaccharides production. These strategies have significant implications for the field of biomaterials.
Non-sulfated forms of glycosaminoglycans (NSGAGs) including hyaluronan, chondroitin and heparosan with high-molecular-weight (HMW) are extensively used biomaterials, while NSGAGs oligosaccharides display strong bioactivities. However, microbial production of HMW-NSGAGs and oligosaccharides with specific size are always challenging. Here, a membrane shield strategy was developed to produce HMW-NSGAGs by recruiting type II NSGAG synthases in Corynebacterium glutamicum. By enhancing precursor supplies and reinforcing cell membrane, the MWs of hyaluronan, heparosan and chondroitin reached 4100 kDa, 3000 kDa and 2400 kDa, respectively. In parallel, a synchronized depolymerization-polymerization strategy was developed by coexpressing NSGAGs synthases and lyases. With cell membrane as a filter, we achieved the direct biosynthesis of NSGAGs tetrasaccharides and disaccharides. The titers of chondroitin, hyaluronan and heparosan tetrasaccharides and disaccharides reached 10.9 g L-1, 12.1 g L-1 and 5.8 g L-1, respectively. The strategies developed here should also be applicable to the biosynthesis of other polysaccharides.

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