Academic Thesis

Basic information

Name Ishihara Koji
Belonging department
Occupation name
researchmap researcher code 1000274244
researchmap agency Okayama University of Science

Title

Biocatalytic Preparation of Chiral Hydroxy Esters using Entomogenous Fungi: Bio-reduction of Keto Esters by Tochukaso and Related Species

Bibliography Type

Joint Author

Author

K. Ishihara, Y. Takaki, N. Masuoka, and K. Shimoda

Summary

To research the potential ability of tochukaso and related species to act as biocatalysts, we screened 10 entomogenous fungal strains. The recommended medium (potato dextrose broth) and a synthetic medium (PGO medium) were tested as the liquid media for culturing these fungi. Four strains (NBRC33061, 100684, 103832, and 109003) cultured using the PGO medium showed a good growth. The stereoselective reduction of a- and b-keto esters by these four strains was also investigated, and they were found to be able to reduce various a-keto esters. Specifically, the reduction of a-keto esters by the PGO-cultivated Isaria cicadae NBRC33061 strain in the presence of L-glutamate as an additive yielded corresponding a-hydroxy esters with a high conversion ratio and in excellent enantioselectivity. Furthermore, it was found that the PGO-cultivated NBRC109003 strain in the presence of L-glutamate stereospecifically reduced ethyl 2-methyl-3-oxobutanoate to (2S, 3S)-2-methyl-3-hydroxybutanoate, i.e., only one of the four theoretically possible isomers. Overall, tochukaso and related species were shown to have a great potential for application as biocatalysts for the stereoselective reduction of carbonyl compounds.

Magazine(name)

International Journal of Current Microbiology and Applied Sciences

Publisher

Excellent Publishers

Volume

13

Number Of Pages

6

StartingPage

155

EndingPage

163

Date of Issue

2024/06

Referee

Exist

Invited

Not exist

Language

English

Thesis Type

Research papers (academic journals)

ISSN

2319-7706(On-line)

DOI

https://doi.org/10.20546/ijcmas.2024.1306.017

NAID

PMID

URL

J-GLOBAL ID

arXiv ID

ORCID Put Code

DBLP ID