Introduction to Enzyme and Coenzyme Chemistry - E-Library Home
Introduction to Enzyme and Coenzyme Chemistry - E-Library Home
Introduction to Enzyme and Coenzyme Chemistry - E-Library Home
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
286 Index<br />
b-hydroxydecanoyl thioester dehydratase 196,<br />
197<br />
b-hydroxydecanoyl thioester isomerase 232<br />
b-sheet 14–17<br />
flavodoxin 18<br />
superoxide dismutase 19<br />
b-turn 14, 16<br />
bifunctional catalysis 40<br />
biosynthesis<br />
acyl transfer reactions 99<br />
alkaloids 222<br />
biotechnology industry 5–6<br />
importance of enzymes 3–7<br />
biotin 170–71, 172<br />
biotin synthase insertion reactions 249–50<br />
bovine trypsin 85<br />
Cahn–Ingold–Prelog rule 61, 272–3<br />
camphor 179–80<br />
camphor, stereospecific hydroxylation of 65,<br />
145<br />
Cannizzaro reaction 127, 128<br />
carbanions <strong>and</strong> carbocations see under<br />
carbon–carbon bond<br />
carbohydrates 24–5, 109<br />
carbon cycle 171<br />
carbon–carbon bond formation 156–87<br />
via carbanion equivalents 156, 158–79<br />
via carbocation (carbonium ion)<br />
intermediates 156, 179–83<br />
via radical intermediates 183–7<br />
carbonium ions see under carbon–carbon bond<br />
carboxylases<br />
biotin dependent 170–71, 172<br />
Rubisco 171–3<br />
vitamin K-dependent 173–5<br />
carboxypeptidase A 46, 93, 94<br />
carboxyphosphate 171<br />
case studies<br />
aspartate aminotransferase 215–18<br />
chorismate mutase 233–6<br />
EPSP synthase 204–6<br />
fruc<strong>to</strong>se-1,6-bisphosphate aldolase 158–63<br />
glutathione <strong>and</strong> trypanothione<br />
reductases 137–41<br />
HIV-1 protease 96–8<br />
catalysis, enzymatic 2<br />
acid/base 37–41<br />
active site group determination 75–9<br />
bifunctional 40<br />
demonstration of 275<br />
efficiencies 47, 56<br />
nucleophilic 41–5<br />
<strong>and</strong> protein dynamics 47<br />
radicals in 240–52<br />
strain energy 45, 111<br />
thermodynamic model 31<br />
catalysis, non-enzymatic biological 255–70<br />
catalytic antibodies 259–65<br />
catalytic polymers 269<br />
catalytic RNA 255–9<br />
synthetic enzyme models 265–9<br />
catalytic efficiency 46, 56<br />
catechol dioxygenases 148, 150, 151<br />
chalcone synthase 188<br />
chelating agents 92<br />
chemical competence 71<br />
chiral methyl groups 65–7, 113<br />
chiral molecules 8<br />
chiral products 61–2<br />
nomenclature 61, 272–3<br />
<strong>and</strong> stereochemical course of reaction 60–67<br />
chloromethyl ke<strong>to</strong>ne inhibi<strong>to</strong>rs 86<br />
chloroperoxidases 145<br />
chorismate mutase 233–6<br />
chorismate synthase 203<br />
chorismic acid 203, 208<br />
chymotrypsin 84–6, 88, 89, 116<br />
citrate synthase 165<br />
citric acid cycle 196, 198<br />
Claisen enzymes 164–70<br />
Claisen ester condensation 164, 166<br />
codons 11–12<br />
coenzyme A (CoA)<br />
in acyl transfer 99–101<br />
see also acetyl CoA<br />
coenzymes 3–4<br />
cofac<strong>to</strong>rs 20, 250–51<br />
collagen 148<br />
coniferyl alcohol 186<br />
convergent evolution 88–9<br />
copper ions 147, 184–5<br />
covalent modification 75, 76<br />
crown ethers 266, 267<br />
cyclisation reactions 264–5<br />
cyclodextrins 266–9<br />
cyclohexanone mono-oxygenase 136, 137<br />
cyclosporin A 5<br />
cysteine proteases 89–92, 117<br />
cysteinyl radical 244–5