A novel fusion levansucrase improves thermostability of polymerization and production of high molecular weight levan. (October 2021)
- Record Type:
- Journal Article
- Title:
- A novel fusion levansucrase improves thermostability of polymerization and production of high molecular weight levan. (October 2021)
- Main Title:
- A novel fusion levansucrase improves thermostability of polymerization and production of high molecular weight levan
- Authors:
- Zhang, Xi
Liang, Yuezhao
Yang, Haibo
Yang, Hui
Chen, Shuochang
Huang, Fei
Hou, Yuanyuan
Huang, Ribo - Abstract:
- Abstract: A novel fusion levansucrase (TPS-SacB-T305A) was constructed by adding to SacB-T305A an extra C-terminus of the trehalose-6-phosphate synthase (TPS) involved in its thermostability. The fusion TPS-SacB-T305A was expressed in Escherichia coli and purified, its hydrolytic V max and K m were about 39.53 μmol/(minute*mg protein) and 13.36 mmol/L, respectively. The levan production reached 71.6 ± 2.06 g/L with a conversion yield of 35.8 ± 1.03% using sucrose as substrates under the present optimum condition of polymerization and the products were characterized by NMR and FT-IR. Interestingly, the optimum temperature of fused TPS-SacB-T305A was 15 °C higher than that of free SacB-T305A on levan polymerization, and the half-life at 40 °C of fusion enzyme increased to more than 4-fold. The proportion of high molecular weight (HMW) levan (approximately 2000 kDa) to total polysaccharides was raised tremendously from approximately 4% (catalyzed by free SacB-T305A) to approximately 91% (catalyzed by TPS-SacB-T305A). The present study provides a potential industrial enzyme to produce HMW levan and helps to explore the mechanism of levan polymerization. Graphical abstract: Image 1 Highlights: Constructed a thermostable fusion enzyme for high molecular weight (HMW) levan production. Half-life for polymerization at 40 °C of fusion enzyme increased to more than 4-fold. The optimum polymerization temperature of fusion enzyme reached 45 °C. The conversion yield of sucrose to levanAbstract: A novel fusion levansucrase (TPS-SacB-T305A) was constructed by adding to SacB-T305A an extra C-terminus of the trehalose-6-phosphate synthase (TPS) involved in its thermostability. The fusion TPS-SacB-T305A was expressed in Escherichia coli and purified, its hydrolytic V max and K m were about 39.53 μmol/(minute*mg protein) and 13.36 mmol/L, respectively. The levan production reached 71.6 ± 2.06 g/L with a conversion yield of 35.8 ± 1.03% using sucrose as substrates under the present optimum condition of polymerization and the products were characterized by NMR and FT-IR. Interestingly, the optimum temperature of fused TPS-SacB-T305A was 15 °C higher than that of free SacB-T305A on levan polymerization, and the half-life at 40 °C of fusion enzyme increased to more than 4-fold. The proportion of high molecular weight (HMW) levan (approximately 2000 kDa) to total polysaccharides was raised tremendously from approximately 4% (catalyzed by free SacB-T305A) to approximately 91% (catalyzed by TPS-SacB-T305A). The present study provides a potential industrial enzyme to produce HMW levan and helps to explore the mechanism of levan polymerization. Graphical abstract: Image 1 Highlights: Constructed a thermostable fusion enzyme for high molecular weight (HMW) levan production. Half-life for polymerization at 40 °C of fusion enzyme increased to more than 4-fold. The optimum polymerization temperature of fusion enzyme reached 45 °C. The conversion yield of sucrose to levan reached 35.8 ± 1.03%. Increased the proportion of HMW levan to total products from approximately 4%–91%. … (more)
- Is Part Of:
- Lebensmittel-Wissenschaft + Technologie =. Volume 150(2021)
- Journal:
- Lebensmittel-Wissenschaft + Technologie =
- Issue:
- Volume 150(2021)
- Issue Display:
- Volume 150, Issue 2021 (2021)
- Year:
- 2021
- Volume:
- 150
- Issue:
- 2021
- Issue Sort Value:
- 2021-0150-2021-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-10
- Subjects:
- Levansucrase -- Fusion -- High molecular weight -- Levan -- Thermostability
Food industry and trade -- Periodicals
Food -- Composition -- Periodicals
Microbiology -- Periodicals
Nutrition -- Periodicals
664.005 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00236438 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.lwt.2021.111951 ↗
- Languages:
- English
- ISSNs:
- 0023-6438
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3983.070000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 18376.xml