Part 1, Enantioselectivity of hydroxy methionine (HMB) incorporation in short chain peptides; Part 2, Development of an enzymatic process for isolation of enantio enriched HMB on a preparative scale; Part 3, Synthesis and characterization of tailored short chain hetero peptides

Author

Arindam Roy

Keywords and Phrases

Enzyme hydrolysis; Short chain peptides

Abstract

"The first part of the dissertation was directed towards determination of enantio selectivity of enzyme catalyzed incorporation of methionine hydroxy analog (HMB) in oligo peptide chains...The second part of the dissertation deals with the development of a technique for enantio-enrichment of HMB...The last part of the research examined a novel approach for the synthesis of the short chain peptides with desired amino acid composition."--Abstract, page iii.

Department(s)

Chemistry

Degree Name

Ph. D. in Chemistry

Publisher

University of Missouri--Rolla

Publication Date

Fall 2003

Pagination

xiv, 156 pages

Note about bibliography

Includes bibliographical references (pages 144-155).

Rights

© 2003 Arindam Roy, All rights reserved.

Document Type

Dissertation - Citation

File Type

text

Language

English

Subject Headings

Liquid chromatographyChiralityEnantiomers -- SeparationPeptides

Thesis Number

T 8372

Print OCLC #

56387543

Recommended Citation

Roy, Arindam, "Part 1, Enantioselectivity of hydroxy methionine (HMB) incorporation in short chain peptides; Part 2, Development of an enzymatic process for isolation of enantio enriched HMB on a preparative scale; Part 3, Synthesis and characterization of tailored short chain hetero peptides" (2003). Doctoral Dissertations. 1517.
https://scholarsmine.mst.edu/doctoral_dissertations/1517