Original ArticleIndian Journal of Pharmaceutical Education and ResearchVol. 51 | Issue 2 | 2017 | pp. 288–294Open access
D-Tagatose production by Lactococcus lactis NZ9000 Cells Harboring Lactobacillus plantarum L-arabinose Isomerase
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- 1 Key Laboratory of Industrial Fermentation Microbiology, Ministry of Education, Tianjin Industrial Microbiology Key Laboratory, College of Biotechnology, Tianjin University of Science and Technology, Tianjin, People’s Republic of CHINA.
Published in Indian Journal of Pharmaceutical Education and Research
Correspondence: Yajian Song
Key Laboratory of Industrial Fermentation Microbiology, Ministry of Education, Tianjin Industrial Microbiology Key Laboratory, College of Biotechnology, Tianjin University of Science and Technology, Tianjin, People’s Republic of CHINA.
Email: songyajian@tust.edu.cn
Copyright: © 2017 Manuscript Technomedia. This is an open access article.
- Published:
- Mar 13, 2017
- Received:
- Aug 30, 2016
- Accepted:
- Nov 23, 2016
How to cite
Zhang, Y., Fan, Y., Hu, H., Yang, H., Luo, X., Li, Z., Zhou, H., Ma, W., Song, Y., & Zhang, T. (2017). D-Tagatose production by Lactococcus lactis NZ9000 Cells Harboring Lactobacillus plantarum L-arabinose Isomerase. Indian Journal of Pharmaceutical Education and Research, 51(2), 288–294. https://doi.org/10.5530/ijper.51.2.34
Abstract
D-tagatose is a functional sweetener present in medicine, food, and dairy products and with broad market prospects, and L-arabinose isomerase gene (araA) can mediate the bioconversion of D-galactose into D-tagatose. In this study, a Lactococcus lactis NZ9000 strain harboring exogenous L-arabinose isomerase was constructed to produce D-tagatose. Lactobacillus plantarum CGMCC 8198 exhibits L-arabinose isomerase activity and its genome has been sequenced. The araA gene of Lactobacillus plantarum CGMCC 8198 encoding L-arabinose isomerase was identified by sequence analysis and was successfully cloned and expressed in Lactococcus lactis NZ9000. The D-tagatose production by the whole cell of the recombinant strain was optimized. The optimal condition for conversion reaction was at 50°C, pH 7.0 and with 300 mmol/L Mn2+ and 60 g/L galactose added. The D-tagatose yield and conversion rate at the optimal condition was determined and reached 40.2 g/L and 67%, respectively.
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Article metadata
| Title | D-Tagatose production by Lactococcus lactis NZ9000 Cells Harboring Lactobacillus plantarum L-arabinose Isomerase |
|---|---|
| Authors | Yao Zhang; Yanli Fan; Haijie Hu; Haixu Yang; Xuegang Luo; Zhongyuan Li; Hao Zhou; Wenjian Ma; Yajian Song; Tongcun Zhang |
| Affiliations | Key Laboratory of Industrial Fermentation Microbiology, Ministry of Education, Tianjin Industrial Microbiology Key Laboratory, College of Biotechnology, Tianjin University of Science and Technology, Tianjin, People’s Republic of CHINA. |
| Corresponding author | songyajian@tust.edu.cn |
| Journal | Indian Journal of Pharmaceutical Education and Research |
| Volume / Issue | Vol. 51, Issue 2 (2017) |
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