TY - CHAP
T1 - Aldolase-Catalyzed C_C Bond Formation of Carbohydrate Synthesis
AU - Sugai, T.
AU - Fuhshuku, K.
PY - 2014/2
Y1 - 2014/2
N2 - 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.
AB - 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.
KW - 3-deoxy-d-manno-2-octusolonic acid aldolase
KW - Aldolase BphI
KW - Deoxyribose-5-phosphate aldolase
KW - Fructose-6-phosphate aldolase
KW - Hydroxynitrile lyase
KW - NAL
KW - Sialic acid aldolase
UR - http://www.scopus.com/inward/record.url?scp=84903502438&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84903502438&partnerID=8YFLogxK
U2 - 10.1016/B978-0-08-097742-3.00212-3
DO - 10.1016/B978-0-08-097742-3.00212-3
M3 - Chapter
AN - SCOPUS:84903502438
SN - 9780080977430
VL - 2
SP - 512
EP - 522
BT - Additions to C-X π-Bonds, Part 2
PB - Elsevier Ltd
ER -