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Acetaldehyde, 2 -deoxyribonucleoside

Scheme 9.1 Multi-step enzymatic process for the production of 2 -deoxyribonucleoside from glucose, acetaldehyde and a nucleobase through the reverse reactions of2 -deoxy-ribonucleoside degradation. Scheme 9.1 Multi-step enzymatic process for the production of 2 -deoxyribonucleoside from glucose, acetaldehyde and a nucleobase through the reverse reactions of2 -deoxy-ribonucleoside degradation.
Biochemical Retrosynthesis of 2 -Deoxyribonucleosides from Glucose Acetaldehyde and a Nucleobase Three-Step Multi-Enzyme-Catalyzed Synthesis... [Pg.204]

Scheme 9.4 Biochemical retrosynthesis of 2 -deoxyribo-nucleosides from glucose, acetaldehyde and a nucleobase (adenine) through the glycolytic pathway and the reverse reactions of 2 -deoxyribonucleoside degradation. Scheme 9.4 Biochemical retrosynthesis of 2 -deoxyribo-nucleosides from glucose, acetaldehyde and a nucleobase (adenine) through the glycolytic pathway and the reverse reactions of 2 -deoxyribonucleoside degradation.
One-Pot Multi-Step Enzymatic Synthesis of 2 -Deoxyribonucleoside from Glucose, Acetaldehyde and a Nucleobase... [Pg.206]

Figure 9.1 2 -Deoxyribonucleoside production from glucose, acetaldehyde and a nucleobase in a one-pot (substrate-feeding) reaction. Figure 9.1 2 -Deoxyribonucleoside production from glucose, acetaldehyde and a nucleobase in a one-pot (substrate-feeding) reaction.
IMPROVEMENT OF THE ONE-POT MULTISTEP ENZYMATIC PROCESS FOR PRACTICAL PRODUCTION OF 2 -DEOXYRIBONUCLEOSIDE FROM GLUCOSE, ACETALDEHYDE, AND A NUCLEOBASE... [Pg.275]

Ogawa, J., K. Saito, T. Sakai, N. Horinouchi, T. Kawano, S. Matsumoto, M. Sasaki, Y. Mikami, and S. Shimizu. 2003. Microbial production of 2-deoxyribose 5-phosphate from acetaldehyde and triosephosphate for the synthesis of 2 -deoxyribonucleosides. Biosci. Biotechnol. Biochem. 67 933-936. [Pg.277]

The 2-deoxy-D-ribose 5-phosphate aldolase (RibA or DERA EC 4.1.2.4) is a class I enzyme that, in vivo, catalyzes the reversible addition of acetaldehyde to D-glyceraldehyde 3-phosphate (34 Figure 5.57) in the metabolic degradation of 127 from deoxyribonucleosides [269], ivith an equilibrium constant for synthesis of 2 x lO m [56]. It is, therefore, unique among the aldolases in that it uses an aldehyde rather than a ketone as the aldol donor. RibA has been isolated from eukaryotic and prokaryotic sources [270, 271],... [Pg.250]

See other pages where Acetaldehyde, 2 -deoxyribonucleoside is mentioned: [Pg.199]    [Pg.200]    [Pg.201]    [Pg.204]    [Pg.205]    [Pg.207]    [Pg.207]    [Pg.208]    [Pg.270]    [Pg.271]    [Pg.273]    [Pg.273]    [Pg.274]    [Pg.275]    [Pg.275]    [Pg.276]    [Pg.416]    [Pg.211]    [Pg.93]   


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Acetaldehyde, 2 -deoxyribonucleoside synthesis

Deoxyribonucleoside

Deoxyribonucleosides

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