The principal investigator states that this research will develop enzymatic catalysts for the synthesis of bioactive molecules and will focus on the following programs: 1. Develop catalytic asymmetric aldol condensations based on aldolases for the synthesis of monosaccharides, carbocycles and analogs. 2. Develop asymmetric glycosylations based on glycosyltransferases for the synthesis of oligosaccharides and nucleosides. 3. Use genetic engineering to improve the production and performance of synthetically useful enzymes, particularly subtilisin, glycosyltransferases, and aldolases. 4. Develop new methods for using enzyme products for synthesis of natural products and designed molecules; glycosidase and glycosyltransferase inhibitors, novel sugars and oligosaccharides, carbocyclic derivatives of sugars, antibiotics and glycopeptides. 5. Provide other enzymatic and non-enzymatic reactions, NMR and modeling techniques to support these efforts in synthesis and molecular design.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM044154-10
Application #
2770967
Study Section
Special Emphasis Panel (ZRG3-MCHA (01))
Project Start
1989-09-01
Project End
2000-08-31
Budget Start
1998-09-01
Budget End
1999-08-31
Support Year
10
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Scripps Research Institute
Department
Type
DUNS #
City
La Jolla
State
CA
Country
United States
Zip Code
92037
Lewis, Jared C; Bastian, Sabine; Bennett, Clay S et al. (2009) Chemoenzymatic elaboration of monosaccharides using engineered cytochrome P450BM3 demethylases. Proc Natl Acad Sci U S A 106:16550-5
Hanson, Sarah R; Culyba, Elizabeth K; Hsu, Tsui-Ling et al. (2009) The core trisaccharide of an N-linked glycoprotein intrinsically accelerates folding and enhances stability. Proc Natl Acad Sci U S A 106:3131-6