Sensual massage : a lover's guide by SUSAN MUMFORD

By SUSAN MUMFORD

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571) R ~HEB Aldolases in saccharides, nature's major way to make C-C bonds cO -----,>- 0 II HNAN>(oe R-C-R' II o Decarboxylation of ~-activated acids, Krebs cycle (p. 25) Biotin carboxylation (or dicarboxylation) dependent enzyme, "activated C02" (p. 1 (continued) Aldol condensation, retro aldol, formation and cleavage of C--C bonds Reductive decarboxylation of a-keto acids, benzoin condensation Decarboxylation of ~-keto and ~-hydroxy acids, cleavage of a C-C bond Addition of C02, formation of a C--C bond, DCC-like intermediate Bayer-Villiger reaction, oxygen insertion VJ '" ~ ~.

In turn, each aminoacyltRNA synthetase enzyme will accept only its particular amino acid as a substrate. However, it has been possible to slightly modify the naturally occurring amino acids and have them serve as substrates for the enzyme. For example, p-fluorophenylalanine can substitute to some extent for phenylalanine. 3 Chemistry of the Peptide Bond R-CH / Cooe ""'NH 3 $ 39 + ATP + tRNA(3'-OH) amino acid -pp I ll Mg 2 • amlnoacyl-tRNA synthetase intermediate anhydride /OH tRNA ll-AMP o H3 R"", II CH-C-O-tRNA N/ aminoacyl-tRNA Once synthesis of the aminoacyl-tRNA is complete, the amino acid no longer serves a recognition function.

G o· IJj '" S p.. o·~ ~ S o· 0> ~ =s 0 ad 0> ... o ~ ~ N N R' (p. 186) 0 .. _) Thiamine-pyrophosphate-dependent decarboxylase, "biological cyanide ion" (p. 571) R ~HEB Aldolases in saccharides, nature's major way to make C-C bonds cO -----,>- 0 II HNAN>(oe R-C-R' II o Decarboxylation of ~-activated acids, Krebs cycle (p. 25) Biotin carboxylation (or dicarboxylation) dependent enzyme, "activated C02" (p. 1 (continued) Aldol condensation, retro aldol, formation and cleavage of C--C bonds Reductive decarboxylation of a-keto acids, benzoin condensation Decarboxylation of ~-keto and ~-hydroxy acids, cleavage of a C-C bond Addition of C02, formation of a C--C bond, DCC-like intermediate Bayer-Villiger reaction, oxygen insertion VJ '" ~ ~.

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