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nucleoside ºËÜÕ
Okazaki fragment ¸ÔÆéƬ¶Î
oncogene °©»ùÒò£¬Ô­°©»ùÒò
one carbon unit һ̼µ¥Î»
operator ²Ù×Ý»ùÒò
operon ²Ù×Ý×Ó
orotic acid ÈéÇåËá
ossification ³É¹Ç×÷ÓÃ
oxaloacetic acid ²Ýõ£ÒÒËá
oxidases Ñõ»¯Ã¸Àà
oxidative phosphorylation Ñõ»¯Á×Ëữ
oxidoreductase Ñõ»¯»¹Ô­Ã¸
palindrome »ØÎĽṹ
pancreatic lipase ÒÈÖ¬·¾Ã¸
pantothenic acid ±é¶àËá
pentose ÎìÌÇ
pentose phosphate pathway Á×ËáÎìÌÇ;¾¶
pepsin θµ°°×ø
pepsinogen θµ°°×øԭ
peptide ëÄ
peptide bond ëļü
peptidyl site ëÄ»ùλ»òPλ
peroxidase ¹ýÑõ»¯Îïø
phenylalanine ±½±û°±Ëá
phosphatidic acid Á×Ö¬Ëá
phosphogluconate Á×ËáÆÏÌÑÌÇËá
phospholipase Á×֬ø
plasmid ÖÊÁ£
polycistron ¶à×÷ÓÃ×Ó
polypeptide ¶àëÄ
porphyrin ߲߸
precipitation ³Áµí
preproalbumin ǰÇåµ°°×Ô­
primary structure Ò»¼¶½á¹¹
primase Òý·¢Ã¸
primer ÒýÎï
glucogenic amino acid ÉúÌǰ±»ùËá
glucokinase ÆÏÌÑÌǼ¤Ã¸
gluconeogenesis ÌÇ(Ô­)ÒìÉú×÷ÓÃ
glutamic acid ¹È°±Ëá
glutaminase ¹È°±õ£°·Ã¸
glutamine ¹È°±õ£°·
glutathione ¹Èë׸ÊëÄ
glycerol ¸ÊÓÍ
glycine ¸Ê°±Ëá
glycogen ÌÇÔ­
glycogen phosphorylase ÌÇÔ­Á×Ëữø
glycogen synthase ÌÇÔ­ºÏ³Éø
glycolysis Ìǽͽâ
helicase ½âÁ´Ã¸(½âÐýø)
heme ѪºìËØ
heteroduplex ÔÓ»¯Ë«Á´
hexokinase ¼ºÌǼ¤Ã¸
histamine ×é°·
histidine ×é°±Ëá
housekeeping gene ¹Ü¼Ò»ùÒò
hybridization ÔÓ½»
hydrogen bond Çâ¼ü
hydrolase Ë®½âøÀà
hydroperoxidases Çâ¹ýÑõ»¯Ã¸Àà
hydrophobic bond (hydrophobic interaction) ÊèË®¼ü
hydroxyapatite ôÇÁ×»Òʯ
hydroxymethylglutaryl CoA cleavage enzyme HMG CoAÁѽâø
hydroxymethylglutaryl CoA synthetase HMG CoAºÏø
Hydroxyproline ôǸ¬°±Ëá
acceptor site ÊÜλ
acetone ±ûͪ
activator ¼¤»îµ°°×£¬¼¤»î¼Á£¬»î»¯Îï
adenine (A) ÏÙàÑßÊ
adenosine ÏÙÜÕ
aerobic dehydrogenase ÐèÑõÍÑÇâø
alanine ±û°±Ëá
albumin °×µ°°×£¬Çåµ°°×
allopurinol ±ðàÑßÊ´¼
allosteric effect ±ð¹¹(λ)ЧӦ
allosteric enzyme ±ä¹¹Ã¸£¬±ðλø
allosteric regulation ±ð¹¹µ÷½Ú
amine °·
aminoacyl site A룬°±õ£»ùλ
anticodon ·´ÃÜÂë×Ó
arginine ¾«°±Ëá
ascorbic acid ¿¹»µÑªËá (άÉúËØC)
asparagine Ì춬õ£°·
aspartic acid Ì춬°±Ëá
asymmetric transcription ²»¶Ô³Æ×ªÂ¼
attenuator Ë¥¼õ×Ó
base ¼î»ù
base pairing ¼î»ùÅä¶Ô
bile pigment µ¨É«ËØ
biotin ÉúÎïËØ
biotransformation ÉúÎïת»¯
calcitriol £±£¬£²£µ¶þôǵ¨¹Ç»¯´¼£¨¸ÆÈý´¼£©
calcium dependent protein kinase CaÒÀÀµÐÔµ°°×¼¤Ã¸£¬µ°°×¼¤Ã¸C(C¼¤Ã¸)
Calmodulin
carbohydrate ÌÇ
carnitine Èâ¶¾¼î
catalase ´¥Ã¸£¬¹ýÑõ»¯Çâø
cephalin ÄÔÁ×Ö¬
de novo synthesis ´ÓÍ·ºÏ³É
degradation ½µ½â
denaturation ±äÐÔ
deoxycholic acid ÍÑÑõµ¨Ëá
deoxyribonucleotide ÍÑÑõºËÌǺËÜÕËá  
dialysis ͸Îö
dihydroxyacetone phosphate Á×Ëá¶þôDZûͪ  
disulfide bond ¶þÁò¼ü
DNA polymerase DNA¾ÛºÏø
domain Óò,½á¹¹Óò,¹¦ÄÜÇø
donor site ¸øÎ»
double helix Ë«ÂÝÐý
effector ЧӦÆ÷,ЧӦÎï
elongation ÑÓ³¤
endopeptidase ÄÚëÄø
enhancer ÔöÇ¿×Ó
enolphosphopyruvate Á×ËáÏ©´¼Ê½±ûͪËá  
enzyme ø
essential amino acid ±ØÐè°±»ùËá
essential fatty acid ±ØÐèÖ¬·¾Ëá
exon ÍâÏÔ×Ó
fat Ö¬·¾
feedback inhibition ·´À¡ÒÖÖÆ×÷ÓÃ
feritin Ìúµ°°×
ferrochelatase ÑÇÌúòüºÏø
folic acid Ò¶Ëá
free fatty acid ÓÎÀëÖ¬·¾Ëá
free radicals ×ÔÓÉ»ù
fructose diphosphatase ¹ûÌǶþÁ×Ëáø
gene cloning »ùÒò¿Ë¡
gene expression »ùÒò±í´ï
gene library »ùÒòÎÄ¿â
gene transfer »ùÒòµ¼Èë,ת»ùÒò
genetic code ÒÅ´«ÃÜÂë
genetic engineering »ùÒò¹¤³Ì
genetic recombination »ùÒòÖØ×é
genome ȾɫÌå»ùÒò£¬»ùÒò×é
globin Öéµ°°×
hypocalcemia µÍ¸ÆÑªÖ¢
induction ÓÕµ¼
initiator codon Æð¶¯ÐźÅ,ÆðʼÃÜÂë×Ó
intermediary metabolism Öмä´úл
ionic bond Àë×Ó¼ü
isocitrate dehydrogenase ÒìÄûÃÊËáÍÑÇâø
isoleucine ÒìÁÁ°±Ëá
isomerase Ò칹øÀà
isozyme ͬ¹¤Ã¸
jaundice »Æðã
ketogenic amino acid Éúͪ°±»ùËá
key enzyme ¹Ø¼üø
kinase ¼¤Ã¸
lactate ÈéËáÑÎ
lecithin ÂÑÁ×Ö¬
leucine ÁÁ°±Ëá
ligase Á¬½Óø
linoleate ÑÇÓÍËá
linolenate ÑÇÂéËá
lipoic acid ÁòÐÁËá
lipoid ÀàÖ¬
lipoprotein Ö¬µ°°×
lithocholic acid ʯµ¨Ëá
lyases ÁѺÏøÀà
malate Æ»¹ûËá
malate aspartate shuttle Æ»¹ûËáÌ춬°±Ëá´©Ëó
metabolic regulation ´úлµ÷½Ú
mitogen activated protein kinase ·ÖÁÑÔ­»î»¯µ°°×¼¤Ã¸
mixed function oxidase »ìºÏ¹¦ÄÜÑõ»¯Ã¸
molecular cloning ·Ö×Ó¿Ë¡
molecular disease ·Ö×Ó²¡
monooxygenase µ¥¼ÓÑõø
monooxygenase system µ¥¼ÓÑõøÌåϵ
nicotinamide ÑÌõ£°·£¬Äá¿Ëõ£°·
nitrogen balance µªÆ½ºâ
pyruvate carboxylase ±ûͪËáôÈ»¯Ã¸
pyruvate dehydrogenase complex ±ûͪËáÍÑÇâø¸´ºÏÌå
pyruvate kinase ±ûͪËἤø
quaternary structure Ëļ¶½á¹¹
recombinant DNA ÖØ×éDNA
genetic engineering »ùÒò¹¤³Ì
regulatory gene µ÷½Ú»ùÒò
renaturation ¸´ÐÔ
repair ÐÞ¸´
replication ¸´ÖÆ
repression ×è¶ô
residue ²Ð»ù
respiratory chain ºôÎüÁ´
restriction endonuclease ÏÞÖÆÐÔÄÚÇкËËáø
retinol Êӻƴ¼(άÉúËØA)
reverse transcriptase Äæ×ªÂ¼Ã¸
reverse transcription Äæ×ªÂ¼×÷ÓÃ
salting out ÑÎÎö
salvage pathway ²¹¾È(ÖØÐÂÀûÓÃ);¾¶
screening ɸѡ
secondary structure ¶þ¼¶½á¹¹
semiconservative replication °ë±£Áô¸´ÖÆ
sense strand ÓÐÒâÒåÁ´
sequence ÐòÁÐ
serine Ë¿°±Ëá
signal recognition particle ÐźÅëÄʶ±ð¿ÅÁ£
silencer ÒÖÖÆ×Ó
simple protein µ¥´¿µ°°×ÖÊ
specificity ÌØÒìÐÔ
splicing ¼ô½Ó×÷ÓÃ
squalene öèÏ©
stage specificity ½×¶ÎÌØÒìÐÔ
stercobilinogen ·àµ¨ËØÔ­
stress Ó¦¼¤
structural gene ½á¹¹»ùÒò
substrate ×÷ÓÃÎï
substrate level phosphorylation ×÷ÓÃÎï(µ×Îï)ˮƽÁ×Ëữ
subunit Ñǵ¥Î»£¬ÑÇ»ù
succinate dehydrogenase çúçêËáÍÑÇâø
supersecondary structure ³¬¶þ¼¶½á¹¹
Taurine Å£»ÇËá
telomerase ¶ËÁ£Ã¸
telomere ¶ËÇø(¶ËÁ£)
template strand Ä£°åÁ´
termination ÖÕÖ¹
terminator ÖÕÖ¹×Ó
terminator codon ÖÕÖ¹ÐźÅ
tertiary structure Èý¼¶½á¹¹
thiamine Áò°·ËØ(άÉúËØB1)
threonine ËÕ°±Ëá
thymidine ÐØÜÕ£¬ÐØÏÙà×ऺËÜÕ
thymine (T) ÐØÏÙà×à¤
tocopherol ÉúÓý·Ó
proalbumin Çåµ°°×Ô­
processing ¼Ó¹¤
proenzyme øԭ
proline ¸¬°±Ëá
promoter Æô¶¯»ùÒò (Æô¶¯×Ó)£¬´ß»¯¼Á
prosthetic group ¸¨»ù
protease µ°°×ø
pyridoxal ßÁ¶ßÈ©
pyridoxamine ßÁ¶ß°·
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