This submission belongs to the session c. Bioorganic Chemistry and Natural Products of the event The 11th International Electronic Conference on Synthetic Organic Chemistry
Published date
30 Nov, 2007
Citation
Amit R. Kumbhar, Vaibhav V. Kulkarni, Madhav B. Pande, Kailas Karande, Sachin S. Laddha, Reductive Biotransformation of Ethyl Acetoacetate: A Comparative Studies using Free and Immobilized Whole Yeast Cells, in Proceedings of The 11th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2007, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-11-01337
Share
Email
Facebook
Twitter
LinkedIn
Reductive Biotransformation of Ethyl Acetoacetate: A Comparative Studies using Free and Immobilized Whole Yeast Cells
Amit R. Kumbhar 1
Vaibhav V. Kulkarni 1
Madhav B. Pande 2
Kailas Karande 3
Sachin S. Laddha 1
1. Biotransformation Lab, Division of Medicinal Chemistry, SVBs College of Pharmacy, MIDC phase II, Sonarpada, Dombivli (E), Dist: Thane 421203, India
2. Department of Biotechnology, Y. T. Institute of Pharmacy, Karjat, Dist: Raigad, India
3. Department of Pharmaceutical Microbiology, Satara College of Pharmacy, Satara-415004, India
Abstract
Bioreduction of ethyl acetoacetate with free and immobilized yeast whole cell was achieved by using water and sucrose combination. After detachment from immobilized beads under basic condition, the corresponding ethyl(S)-(+)-3-hydroxybutanoate was isolated with 98 to 100% yield. Immobilized beads of yeast whole cell were prepared at different temperature which affects the morphology and physiology of the beads for the diffusion of the enzyme, which shown the maximum conversion of the products as compared to the free yeast whole cell.
Keywords
Biotransformation
Ethyl acetoacetate
Ethyl(S)-(+)-3-hydroxybutanoate
Immobilized yeast whole cell
Free yeast whole cell
Synthesis of (HET)ARYLAMIDOGUANIDINES and their Anticoagulant Activity Evaluation
Photocleavage Studies of γ-aminobutyric acid (GABA) Conjugates