EC Number |
Recommended Name |
Source Tissue |
Reference |
---|
1.1.1.267 | 1-deoxy-D-xylulose-5-phosphate reductoisomerase |
pericarp |
- |
720429 |
1.1.1.34 | hydroxymethylglutaryl-CoA reductase (NADPH) |
pericarp |
- |
740956 |
1.14.14.82 | flavonoid 3'-monooxygenase |
pericarp |
- |
675659 |
1.14.15.24 | beta-carotene 3-hydroxylase |
pericarp |
- |
746142 |
1.14.17.4 | aminocyclopropanecarboxylate oxidase |
pericarp |
- |
639298, 639306 |
1.14.18.1 | tyrosinase |
pericarp |
- |
687243 |
1.14.19.41 | sterol 22-desaturase |
pericarp |
- |
734014 |
1.2.3.1 | aldehyde oxidase |
pericarp |
- |
713323 |
2.1.1.158 | 7-methylxanthosine synthase |
pericarp |
- |
-, 670621 |
2.1.1.159 | theobromine synthase |
pericarp |
- |
670621, 734861 |
2.1.1.160 | caffeine synthase |
pericarp |
- |
670621 |
2.1.1.267 | flavonoid 3',5'-methyltransferase |
pericarp |
- |
756307 |
2.1.1.76 | quercetin 3-O-methyltransferase |
pericarp |
- |
756307 |
2.2.1.7 | 1-deoxy-D-xylulose-5-phosphate synthase |
pericarp |
- |
676738 |
2.3.1.220 | 2,4,6-trihydroxybenzophenone synthase |
pericarp |
- |
720639 |
2.3.2.2 | gamma-glutamyltransferase |
pericarp |
- |
723353 |
2.4.1.13 | sucrose synthase |
pericarp |
- |
675142 |
2.4.1.207 | xyloglucan:xyloglucosyl transferase |
pericarp |
- |
694757 |
2.4.1.21 | starch synthase (glycosyl-transferring) |
pericarp |
- |
736155 |
2.4.1.214 | glycoprotein 3-alpha-L-fucosyltransferase |
pericarp |
- |
757946 |
2.4.1.242 | NDP-glucose-starch glucosyltransferase |
pericarp |
- |
660290 |
2.4.1.294 | cyanidin 3-O-galactosyltransferase |
pericarp |
- |
757928 |
2.4.1.91 | flavonol 3-O-glucosyltransferase |
pericarp |
- |
723147 |
2.7.1.4 | fructokinase |
pericarp |
- |
-, 641502, 641510, 641511 |
3.1.1.11 | pectinesterase |
pericarp |
- |
114114, 674118, 729774, 730754 |
3.2.1.14 | chitinase |
pericarp |
- |
656981 |
3.4.22.34 | Legumain |
pericarp |
- |
752851 |
3.6.1.1 | inorganic diphosphatase |
pericarp |
- |
209826 |
4.2.3.119 | (-)-alpha-pinene synthase |
pericarp |
- |
730575, 747887 |
4.2.3.120 | (-)-beta-pinene synthase |
pericarp |
- |
730575, 747887 |
4.2.3.121 | (+)-alpha-pinene synthase |
pericarp |
- |
747887 |
4.2.3.122 | (+)-beta-pinene synthase |
pericarp |
- |
747887 |
4.2.3.13 | (+)-delta-cadinene synthase |
pericarp |
- |
648585 |
4.2.3.89 | (+)-beta-caryophyllene synthase |
pericarp |
- |
748003 |
4.4.1.14 | 1-aminocyclopropane-1-carboxylate synthase |
pericarp |
- |
34565, 34567, 34569, 34571, 34573, 34578, 34584, 694758 |
5.3.99.8 | capsanthin/capsorubin synthase |
pericarp |
- |
746142 |
2.3.2.2 | gamma-glutamyltransferase |
pericarp |
2 isoforms I and II |
487967 |
3.4.22.14 | actinidain |
pericarp |
actinidin is present in small cells, but not large cells in the outer pericarp of mature Actinidia deliciosa fruit at harvest. Within the small cells, actinidin is localised diffusely in the vacuole, associated with the plasma membrane, and in a layer in the plastids near starch granules |
686912 |
3.2.1.2 | beta-amylase |
pericarp |
beta-amylase activity is uniformly shared by endosperm and bran |
730107 |
1.14.14.91 | trans-cinnamate 4-monooxygenase |
pericarp |
BnC4H-1 is dominant over BnC4H-2 |
687469 |
5.3.99.8 | capsanthin/capsorubin synthase |
pericarp |
disc |
660184 |
4.2.3.111 | (-)-alpha-terpineol synthase |
pericarp |
distribution of alpha-terpineol content in the 61 grapevine accessions |
747364 |
1.14.11.13 | gibberellin 2beta-dioxygenase |
pericarp |
elevated PsGA2ox2 transcript levels 2 days prior to anthesis, directly after pollination decrease, removal of seeds 2-3 days after anthesis leads to inhibition of transitory increase of PsGA2ox2 observed in seed-containing pericarps, reduction of PsGA2ox2 by day 5 after anthesis, seed presence represses the expression of PsGA2ox2 during days 5-12 after anthesis |
700830 |
3.2.1.4 | cellulase |
pericarp |
enzyme appears at the stage in which many ripening-related changes start, and remains present throughout fruit ripening |
-, 666678 |
2.3.1.151 | 2,3',4,6-tetrahydroxybenzophenone synthase |
pericarp |
expression of GmBPS in fruit pericarp from an early stage |
720639 |
2.2.1.7 | 1-deoxy-D-xylulose-5-phosphate synthase |
pericarp |
extensively expressed |
720429 |
3.1.7.11 | geranyl diphosphate diphosphatase |
pericarp |
fruit pericarp, low expression level |
750897 |
2.4.1.21 | starch synthase (glycosyl-transferring) |
pericarp |
granule-bound starch synthase II |
488924 |
1.1.1.25 | shikimate dehydrogenase (NADP+) |
pericarp |
high expression is observed for isozyme VvSDH1 before veraison but its maximum expression level is reached after veraison |
740821 |
1.1.1.42 | isocitrate dehydrogenase (NADP+) |
pericarp |
high expression level |
722338 |
1.14.11.13 | gibberellin 2beta-dioxygenase |
pericarp |
high levels of PsGA2ox1 prior to anthesis, reduced increase (15fold) of PsGA2ox1 mRNA levels directly after pollination compared to unpollinated pericarp (50-fold increase), decrease of pollinated and unpollinated levels one day after anthesis and further, concomitant with high pericarp growth rates, removal of seeds 2-3 days after anthesis increases PsGA2ox1 transcript levels compared to seed-containing pericarp, seed presence represses the expression of PsGA2ox1 during days 5-12 after anthesis, unpollinated ovaries degenerate after 4 d |
700830 |
4.2.3.104 | alpha-humulene synthase |
pericarp |
highest expression level |
730575 |
4.2.3.57 | (-)-beta-caryophyllene synthase |
pericarp |
highest expression level |
730575 |
2.4.1.242 | NDP-glucose-starch glucosyltransferase |
pericarp |
isozyme GBSSII |
488924 |
4.2.3.104 | alpha-humulene synthase |
pericarp |
low expression |
730575 |
1.14.14.137 | (+)-abscisic acid 8'-hydroxylase |
pericarp |
low level |
706376 |
1.14.11.13 | gibberellin 2beta-dioxygenase |
pericarp |
major nutrient sink in the developing pea fruit until 8-12 days after pollination |
700830 |
1.14.11.15 | gibberellin 3beta-dioxygenase |
pericarp |
mRNA level is minimally detectable in prepolinated pericarp, increases dramatically after polination, then decreases by by 1 day after anthesis. Expression is hormonally regulated |
660218 |
1.14.11.15 | gibberellin 3beta-dioxygenase |
pericarp |
mRNA levels gradually increases from day 2 to 3 after anthesis when seeds are present. When seeds are removed the pericarp transcript level dramatically declines |
660218 |
2.4.1.13 | sucrose synthase |
pericarp |
mRNA levels of CaSUS2 is barely detectable in young pericarp, but increased towards the ripening of pericarp tissues |
675142 |
4.1.1.31 | phosphoenolpyruvate carboxylase |
pericarp |
pre-climacteric fruit |
4326 |
2.4.1.123 | inositol 3-alpha-galactosyltransferase |
pericarp |
strong expression of BnGolS2 and BnGolS3 members 40 days after flowering |
759361 |
1.1.1.25 | shikimate dehydrogenase (NADP+) |
pericarp |
the VvSDH3 expression level rises during the green stage. At veraison, its expression drops and stays very low throughout the ripening stage |
740821 |
1.1.1.25 | shikimate dehydrogenase (NADP+) |
pericarp |
VvSDH2 expression is relatively stable during grape development, except for a peak of expression before veraison |
740821 |
1.1.1.25 | shikimate dehydrogenase (NADP+) |
pericarp |
VvSDH4 expression is relatively stable during grape development, except for a peak of expression before veraison |
740821 |
1.1.1.34 | hydroxymethylglutaryl-CoA reductase (NADPH) |
pericarp |
young |
722329 |