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Introduction to Enzyme and Coenzyme Chemistry - E-Library Home

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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

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