Novel biocatalytic strategy of levan: His-ELP-intein-tagged protein purification and biomimetic mineralization. (15th July 2022)
- Record Type:
- Journal Article
- Title:
- Novel biocatalytic strategy of levan: His-ELP-intein-tagged protein purification and biomimetic mineralization. (15th July 2022)
- Main Title:
- Novel biocatalytic strategy of levan: His-ELP-intein-tagged protein purification and biomimetic mineralization
- Authors:
- Zhang, Yifeng
Gao, Song
Qi, Xianghui
Zhu, Song
Xu, Shumin
Liang, Yaokun
Kong, Fanshu
Yang, Shuai
Wang, Rui
Wang, Yiting
An, Yingfeng - Abstract:
- Abstract: Here a versatile fusion tag composed of His-tag, intein, and elastin-like polypeptide (ELP) tag was prepared for the first time to be fused with levansucrase SacB to construct a recombinant His-ELP-intein-SacB (HEIS) protein to realize nonchromatographic purification of SacB. The efficient biomimetic mineralization of CaHPO4 and HEIS-based hybrid-hydrangea (CaHPO4 -HEIS-HH) with good reusability, excellent storage stability and 254.3% improved relative levan yield was prepared with the biomimetic mineralization method. Additionally, the CaHPO4 -HEIS-HH showed outstanding operation activity when catalyzing sucrose in solution and up to 75% sucrose conversion rate in fruit juices. The mechanism of biomimetic mineralization was analyzed to show that the HEIS protein might serve as a "binder" to assemble the nanoflakes during biomimetic mineralization. The CaHPO4 -HEIS-HH was applicable for efficient production of the levan-type prebiotic polysaccharides, and this approach should be highly valuable for nonchromatographic purification and convenient preparation of various encapsulated enzymes for more efficient catalysis. Graphical abstract: Unlabelled Image Highlights: A strategy was designed for more efficient nonchromatographic purification of protein. CaHPO4-based biomimetic mineralization of SacB was designed for improved catalysis. The resulting CaHPO4-HEIS-HH was useful for efficient production of prebiotic levan. CaHPO4-HEIS-HH showed up to 75% sucroseAbstract: Here a versatile fusion tag composed of His-tag, intein, and elastin-like polypeptide (ELP) tag was prepared for the first time to be fused with levansucrase SacB to construct a recombinant His-ELP-intein-SacB (HEIS) protein to realize nonchromatographic purification of SacB. The efficient biomimetic mineralization of CaHPO4 and HEIS-based hybrid-hydrangea (CaHPO4 -HEIS-HH) with good reusability, excellent storage stability and 254.3% improved relative levan yield was prepared with the biomimetic mineralization method. Additionally, the CaHPO4 -HEIS-HH showed outstanding operation activity when catalyzing sucrose in solution and up to 75% sucrose conversion rate in fruit juices. The mechanism of biomimetic mineralization was analyzed to show that the HEIS protein might serve as a "binder" to assemble the nanoflakes during biomimetic mineralization. The CaHPO4 -HEIS-HH was applicable for efficient production of the levan-type prebiotic polysaccharides, and this approach should be highly valuable for nonchromatographic purification and convenient preparation of various encapsulated enzymes for more efficient catalysis. Graphical abstract: Unlabelled Image Highlights: A strategy was designed for more efficient nonchromatographic purification of protein. CaHPO4-based biomimetic mineralization of SacB was designed for improved catalysis. The resulting CaHPO4-HEIS-HH was useful for efficient production of prebiotic levan. CaHPO4-HEIS-HH showed up to 75% sucrose conversion within fruit juices of pH 3.0–5.0. The principle of CaHPO4-based biomimetic mineralization was deeply analyzed. … (more)
- Is Part Of:
- Carbohydrate polymers. Volume 288(2022)
- Journal:
- Carbohydrate polymers
- Issue:
- Volume 288(2022)
- Issue Display:
- Volume 288, Issue 2022 (2022)
- Year:
- 2022
- Volume:
- 288
- Issue:
- 2022
- Issue Sort Value:
- 2022-0288-2022-0000
- Page Start:
- Page End:
- Publication Date:
- 2022-07-15
- Subjects:
- Biocatalyst -- Biomimetic mineralization -- Elastin-like polypeptides -- hydrangea -- Levansucrase
Polysaccharides -- Periodicals
Polysaccharides -- Periodicals
Polysaccharides -- Périodiques
Electronic journals
547.78 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01448617 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.carbpol.2022.119398 ↗
- Languages:
- English
- ISSNs:
- 0144-8617
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3050.990480
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21293.xml