Disproportionation reactions catalyzed by Leuconostoc and Streptococcus glucansucrases
✍ Scribed by Thomas P. Binder; Gregory L. Côté; John F. Robyt
- Book ID
- 102993154
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- English
- Weight
- 847 KB
- Volume
- 124
- Category
- Article
- ISSN
- 0008-6215
No coin nor oath required. For personal study only.
✦ Synopsis
Glucansucrases from Leuconostoc mesenteroides NRRL B-512F and Streptococcus mutans 6715 were found to utilize a number of D-gluco-oligosaccharides as D-glucosyl donors and as acceptors . These donors included isomaltotriose and its homologs, panose, maltotriose, and dextran. In each case, D-glucosyl groups were transferred from the donor to an acceptor sugar . When the donor sugar also acted as an acceptor, disproportionation reactions occurred . Isomaltotriose, for example, gave rise to isomaltose and isomaltotetraose initially, and to a series of isomalto-oligosaccharides eventually . In addition to forming a-D-(1-*6) linkages in these reactions, dextransucrase from S. mutans 6715 was capable of forming a-D-(1-*3)-linked products .
📜 SIMILAR VOLUMES
In the light of recent interest in hydrocarbon carbanion reactions in polar solvents (l) we wish to report the discovery of a homogeneous base catalyzed trans-hydrogenation reaction. Kinetics of this reaction indicate that hydride transfer is the rate-determining step. Carbon-carbon hydride transfer