EC Number |
Recommended Name |
Source Tissue |
Reference |
---|
1.3.1.82 | (-)-isopiperitenone reductase |
cell culture |
- |
-, 746552 |
5.4.99.15 | (1->4)-alpha-D-glucan 1-alpha-D-glucosylmutase |
cell culture |
10fold increase of enzyme activity in soybean nodules infected with Bradyrhizobium japonicum compared to bacterial culture |
677667 |
5.4.99.15 | (1->4)-alpha-D-glucan 1-alpha-D-glucosylmutase |
cell culture |
8fold increase of enzyme activity in soybean nodules infected with Bradyrhizobium elkanii compared to bacterial culture |
677667 |
4.2.3.20 | (R)-limonene synthase |
cell culture |
- |
691407 |
1.1.1.4 | (R,R)-butanediol dehydrogenase |
cell culture |
- |
-, 722559 |
2.1.1.115 | (RS)-1-benzyl-1,2,3,4-tetrahydroisoquinoline N-methyltransferase |
cell culture |
- |
15190 |
2.1.1.128 | (RS)-norcoclaurine 6-O-methyltransferase |
cell culture |
- |
15229, 15232 |
1.1.3.15 | (S)-2-hydroxy-acid oxidase |
cell culture |
- |
389675, 389699 |
1.14.19.68 | (S)-canadine synthase |
cell culture |
- |
15195, 393236 |
1.14.19.68 | (S)-canadine synthase |
cell culture |
protoberberine producing cell line |
393236 |
2.1.1.140 | (S)-coclaurine-N-methyltransferase |
cell culture |
- |
15231, 288659, 659190, 687805 |
1.14.19.51 | (S)-corytuberine synthase |
cell culture |
- |
687805 |
4.2.1.78 | (S)-norcoclaurine synthase |
cell culture |
- |
5894, 5895, 716518 |
2.1.1.117 | (S)-scoulerine 9-O-methyltransferase |
cell culture |
- |
15196 |
2.1.1.117 | (S)-scoulerine 9-O-methyltransferase |
cell culture |
activity of high berberine-producing cells is higher than that of non-selected cells |
15192 |
2.1.1.122 | (S)-tetrahydroprotoberberine N-methyltransferase |
cell culture |
elicitor treatment |
674802 |
2.4.1.97 | 1,3-beta-D-glucan phosphorylase |
cell culture |
- |
639635 |
2.4.1.34 | 1,3-beta-glucan synthase |
cell culture |
budding and filamentous |
489064 |
2.4.1.18 | 1,4-alpha-glucan branching enzyme |
cell culture |
- |
706685 |
4.1.3.36 | 1,4-dihydroxy-2-naphthoyl-CoA synthase |
cell culture |
- |
93959 |
2.3.1.51 | 1-acylglycerol-3-phosphate O-acyltransferase |
cell culture |
- |
687624, 687813 |
2.3.1.23 | 1-acylglycerophosphocholine O-acyltransferase |
cell culture |
endothelial cells |
486644 |
3.5.99.7 | 1-aminocyclopropane-1-carboxylate deaminase |
cell culture |
- |
693861 |
3.5.99.7 | 1-aminocyclopropane-1-carboxylate deaminase |
cell culture |
four different morphotypes of biovar B, strain HS-2 and the strain UW4 as control strain |
691950 |
3.5.99.7 | 1-aminocyclopropane-1-carboxylate deaminase |
cell culture |
strain UW4 |
-, 694780 |
3.5.99.7 | 1-aminocyclopropane-1-carboxylate deaminase |
cell culture |
strain UW4 AcdS+ (ability to synthesize ACC deaminase and indole acetic acid) and its mutant strain AcdS- |
-, 692374 |
2.2.1.7 | 1-deoxy-D-xylulose-5-phosphate synthase |
cell culture |
- |
676738 |
2.7.1.68 | 1-phosphatidylinositol-4-phosphate 5-kinase |
cell culture |
Escherichia coli BL21 cell is used for cloning and expression |
689477 |
2.7.1.149 | 1-phosphatidylinositol-5-phosphate 4-kinase |
cell culture |
DT40 cell from chicken, that expresses active PIPkin IIbetA tagged at the C-terminus of Hef, a protein component of the Fanconi anemia-related tumor-suppressor complex. |
686033 |
2.1.1.120 | 12-hydroxydihydrochelirubine 12-O-methyltransferase |
cell culture |
- |
7393 |
2.1.1.170 | 16S rRNA (guanine527-N7)-methyltransferase |
cell culture |
activity of rsmGp slightly increases by fourfold when cells are grown in minimal media supplemented with glycerol instead of glucose |
721042 |
2.7.7.84 | 2'-5' oligoadenylate synthase |
cell culture |
- |
721471 |
2.7.7.84 | 2'-5' oligoadenylate synthase |
cell culture |
from spleen |
721471 |
1.3.1.51 | 2'-hydroxydaidzein reductase |
cell culture |
elicitor-induced |
12301 |
1.3.1.45 | 2'-hydroxyisoflavone reductase |
cell culture |
constitutive expression |
656914 |
2.3.1.151 | 2,3',4,6-tetrahydroxybenzophenone synthase |
cell culture |
- |
16326, 660170, 706131 |
1.13.11.9 | 2,5-dihydroxypyridine 5,6-dioxygenase |
cell culture |
pyridine-2,6-dicarboxylic acid- and pyridine-2,3-dicarboxylic acid-induced strain 23K8 cells. The cells do not grow on pyridine-2,5-dicarboxylic acid |
-, 742294 |
1.1.1.268 | 2-(R)-hydroxypropyl-CoM dehydrogenase |
cell culture |
- |
-, 288637 |
1.1.1.268 | 2-(R)-hydroxypropyl-CoM dehydrogenase |
cell culture |
metabolism of propylene depends on the presence of a linear megaplasmid, that encodes enzymes of alkene oxidation, epoxide carboxylation and CoM biosynthesis |
-, 389508 |
1.1.1.269 | 2-(S)-hydroxypropyl-CoM dehydrogenase |
cell culture |
metabolism of propylene depends on the presence of a linear megaplasmid, that encodes enzymes of alkene oxidation, epoxide carboxylation and CoM biosynthesis |
-, 389508 |
2.2.1.10 | 2-amino-3,7-dideoxy-D-threo-hept-6-ulosonate synthase |
cell culture |
optimal growth temperature is 85°C |
692386 |
1.1.1.127 | 2-dehydro-3-deoxy-D-gluconate 5-dehydrogenase |
cell culture |
- |
285820, 285821 |
1.1.1.126 | 2-dehydro-3-deoxy-D-gluconate 6-dehydrogenase |
cell culture |
inducible enzyme synthesis by growth in alginate-containing medium |
285819 |
1.1.1.125 | 2-deoxy-D-gluconate 3-dehydrogenase |
cell culture |
inducible enzyme synthesis by growth in 2-deoxy-D-gluconate containing medium |
285818 |
1.1.1.312 | 2-hydroxy-4-carboxymuconate semialdehyde hemiacetal dehydrogenase |
cell culture |
- |
-, 671526 |
4.2.1.105 | 2-hydroxyisoflavanone dehydratase |
cell culture |
- |
656937 |
5.3.2.6 | 2-hydroxymuconate tautomerase |
cell culture |
strain JJ-1b is able to grow on 4-hydroxybenzoate as a sole source of carbon and energy |
704310 |
2.1.1.116 | 3'-hydroxy-N-methyl-(S)-coclaurine 4'-O-methyltransferase |
cell culture |
- |
15191 |
3.1.3.6 | 3'-nucleotidase |
cell culture |
- |
95079 |
2.3.1.177 | 3,5-dihydroxybiphenyl synthase |
cell culture |
- |
718719, 720794 |
2.3.1.177 | 3,5-dihydroxybiphenyl synthase |
cell culture |
yeast-extract-treated |
663182 |
1.14.14.93 | 3,9-dihydroxypterocarpan 6a-monooxygenase |
cell culture |
- |
390057, 390058, 390062 |
1.1.1.130 | 3-dehydro-L-gulonate 2-dehydrogenase |
cell culture |
- |
285827 |
4.2.1.118 | 3-dehydroshikimate dehydratase |
cell culture |
cultured in presence of shikimate |
700722 |
2.5.1.54 | 3-deoxy-7-phosphoheptulonate synthase |
cell culture |
- |
639755, 639765, 639773, 639780 |
1.1.1.31 | 3-hydroxyisobutyrate dehydrogenase |
cell culture |
astroglia-rich primary culture from neonatal rats |
688515 |
1.1.1.259 | 3-hydroxypimeloyl-CoA dehydrogenase |
cell culture |
- |
-, 207950, 207951, 207952 |
1.1.1.265 | 3-methylbutanal reductase |
cell culture |
- |
246373, 246375, 286203 |
2.8.3.5 | 3-oxoacid CoA-transferase |
cell culture |
- |
645977 |
1.1.1.100 | 3-oxoacyl-[acyl-carrier-protein] reductase |
cell culture |
strain KCTC1639 |
693287 |
3.1.3.8 | 3-phytase |
cell culture |
fermentation is optimized by a response surface methodology based on the Box-Behnken design, production leads to maximum activity of phytase of 205.45 U/ml |
-, 750979 |
3.1.3.8 | 3-phytase |
cell culture |
phytase increases markedly at the late stationary phase |
-, 653032 |
1.1.1.152 | 3alpha-hydroxy-5beta-androstane-17-one 3alpha-dehydrogenase |
cell culture |
- |
286009 |
1.14.14.89 | 4'-methoxyisoflavone 2'-hydroxylase |
cell culture |
suspension |
285318 |
2.7.1.148 | 4-(cytidine 5'-diphospho)-2-C-methyl-D-erythritol kinase |
cell culture |
cloned in Escherichia coli |
686699 |
1.1.1.257 | 4-(hydroxymethyl)benzenesulfonate dehydrogenase |
cell culture |
- |
-, 207945, 207946, 207947, 207948, 207949 |
2.6.1.19 | 4-aminobutyrate-2-oxoglutarate transaminase |
cell culture |
- |
698627 |
2.6.1.19 | 4-aminobutyrate-2-oxoglutarate transaminase |
cell culture |
growth at temperatures of up to 50°C |
-, 759234 |
3.8.1.7 | 4-chlorobenzoyl-CoA dehalogenase |
cell culture |
strain P25 utilizes 4-chlorobiphenyl and 4-chlorobenzoic acid as sole carbon and energy sources |
-, 720401 |
6.2.1.12 | 4-coumarate-CoA ligase |
cell culture |
- |
602, 603, 606, 608, 611, 728204 |
1.2.1.62 | 4-formylbenzenesulfonate dehydrogenase |
cell culture |
- |
-, 207945, 207946, 207947 |
1.2.1.64 | 4-hydroxybenzaldehyde dehydrogenase (NAD+) |
cell culture |
- |
-, 288311, 288313 |
1.2.1.96 | 4-hydroxybenzaldehyde dehydrogenase (NADP+) |
cell culture |
- |
-, 288312, 288314 |
2.3.1.208 | 4-hydroxycoumarin synthase |
cell culture |
elicitor-treated |
706131, 706258 |
2.3.1.208 | 4-hydroxycoumarin synthase |
cell culture |
elicitor-treated cell cultures |
721091 |
1.2.1.61 | 4-hydroxymuconic-semialdehyde dehydrogenase |
cell culture |
- |
288304 |
1.13.11.27 | 4-hydroxyphenylpyruvate dioxygenase |
cell culture |
- |
395387 |
3.1.3.26 | 4-phytase |
cell culture |
fermentation is optimized by a response surface methodology based on the Box-Behnken design, production leads to maximum activity of phytase of 205.45 U/ml |
-, 750979 |
3.1.3.26 | 4-phytase |
cell culture |
phytase increases markedly at the late stationary phase |
-, 653032 |
3.1.3.5 | 5'-nucleotidase |
cell culture |
from submandibular salivary glands |
664550 |
1.1.1.193 | 5-amino-6-(5-phosphoribosylamino)uracil reductase |
cell culture |
- |
-, 246736 |
2.3.1.37 | 5-aminolevulinate synthase |
cell culture |
- |
486815 |
2.3.1.37 | 5-aminolevulinate synthase |
cell culture |
high activity in cells grown anaerobically in defined medium, low in cells grown in an iron-deficient medium and in cells grown aerobically |
486810 |
1.2.1.60 | 5-carboxymethyl-2-hydroxymuconic-semialdehyde dehydrogenase |
cell culture |
- |
-, 288040, 288297, 288298, 288299, 288300, 288301 |
1.2.1.60 | 5-carboxymethyl-2-hydroxymuconic-semialdehyde dehydrogenase |
cell culture |
strict dependency for induction of enzyme synthesis of the meta-cleavage pathway by 4-hydroxyphenylacetate |
-, 288303 |
2.1.1.69 | 5-hydroxyfuranocoumarin 5-O-methyltransferase |
cell culture |
- |
485550 |
2.1.1.14 | 5-methyltetrahydropteroyltriglutamate-homocysteine S-methyltransferase |
cell culture |
- |
441337 |
1.14.14.96 | 5-O-(4-coumaroyl)-D-quinate 3'-monooxygenase |
cell culture |
- |
395989 |
3.5.1.46 | 6-aminohexanoate-oligomer exohydrolase |
cell culture |
- |
-, 172039, 172042, 172043 |
3.5.1.46 | 6-aminohexanoate-oligomer exohydrolase |
cell culture |
nylB gene, enzyme EII |
-, 172040, 172041 |
3.5.1.46 | 6-aminohexanoate-oligomer exohydrolase |
cell culture |
nylB' gene, enzyme EII' |
-, 172040, 172041 |
6.2.1.14 | 6-carboxyhexanoate-CoA ligase |
cell culture |
- |
-, 630, 649669 |
3.7.1.18 | 6-oxocamphor hydrolase |
cell culture |
strain NCIMB 9784 is grown on (1R)-(+)-camphor as the sole carbon source |
-, 719804 |
1.2.1.63 | 6-oxohexanoate dehydrogenase |
cell culture |
- |
-, 288310, 7430 |
1.2.1.63 | 6-oxohexanoate dehydrogenase |
cell culture |
inducible enzyme synthesis by growth in cyclohexanol |
-, 246371 |
1.2.1.63 | 6-oxohexanoate dehydrogenase |
cell culture |
strain TD63 only inducible for enzyme synthesis in the presence of trans-cyclohexan-1,2-diol-containing growth media |
-, 7430 |
3.2.1.85 | 6-phospho-beta-galactosidase |
cell culture |
activity is induced during growth on lactose but is absent in glucose-grown cells |
677688 |
2.7.1.105 | 6-phosphofructo-2-kinase |
cell culture |
- |
661569 |
4.2.3.12 | 6-pyruvoyltetrahydropterin synthase |
cell culture |
the starting cells, which are harvested just after plating on the developmental plate exhibit high PTPS mRNA. After 4 h, the transcripts decrease dramatically and then remain at the levels thereafter, although increases slightly at the terminal stage (after 12 h) |
-, 667828 |
1.14.14.85 | 7-deoxyloganate 7-hydroxylase |
cell culture |
- |
437786, 440296 |