Abstract
Three types of aldolase-catalyzed reactions which are promising for C. C bond formation, not only for the practical synthesis of carbohydrates but also in active pharmaceutical ingredients manufacturing, were introduced. The authors focused on the use of three nonphosphorylated nucleophiles: pyruvic acid, acetaldehyde, and dihydroxyacetone. Furthermore, nitroaldol reaction catalyzed by hydroxynitrile lyase (HNL) is noted as an example of catalysis caused by the promiscuous ability of enzymes. All of following the aspects involving screening of new enzymes, characterization, substrate specificity study, synthetic application, and protein engineering are very important in developing improved biocatalytic processes.
Original language | English |
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Title of host publication | Additions to C-X π-Bonds, Part 2 |
Publisher | Elsevier Ltd |
Pages | 512-522 |
Number of pages | 11 |
Volume | 2 |
ISBN (Print) | 9780080977430 |
DOIs | |
Publication status | Published - 2014 Feb |
Keywords
- 3-deoxy-d-manno-2-octusolonic acid aldolase
- Aldolase BphI
- Deoxyribose-5-phosphate aldolase
- Fructose-6-phosphate aldolase
- Hydroxynitrile lyase
- NAL
- Sialic acid aldolase
ASJC Scopus subject areas
- Chemical Engineering(all)
- Chemistry(all)