Any feedback?
Enzyme Nomenclature
Information on EC 1.13.11.70 - all-trans-10'-apo-beta-carotenal 13,14-cleaving dioxygenase
for references in articles please use BRENDA:EC1.13.11.70Please wait a moment until all data is loaded. This message will disappear when all data is loaded.
EC Tree
1.13.11.70 all-trans-10'-apo-beta-carotenal 13,14-cleaving dioxygenaseIUBMB Comments
Requires Fe2+. The enzyme from the plant Arabidopsis thaliana also catalyses EC 1.13.11.69, carlactone synthase, 10-fold faster.
Specify your search results
The enzyme appears in viruses and cellular organisms
Reaction Schemes
topPlease wait a moment until the data is sorted. This message will disappear when the data is sorted.
SYNONYM 
ORGANISM
UNIPROT
COMMENTARY 
LITERATURE
carotenoid cleavage dioxygenase
CCD8
MAX4
NCED8
-
-
-
-
CCD8
-
-
-
-
MAX4
-
-
-
-
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
REACTION
REACTION DIAGRAM
COMMENTARY
ORGANISM
UNIPROT
LITERATURE
all-trans-10'-apo-beta-carotenal + O2 = 13-apo-beta-carotenone + (2E,4E,6E)-4-methylocta-2,4,6-trienedial
all-trans-10'-apo-beta-carotenal + O2 = 13-apo-beta-carotenone + (2E,4E,6E)-4-methylocta-2,4,6-trienedial
-
-
-
-
all-trans-10'-apo-beta-carotenal + O2 = 13-apo-beta-carotenone + (2E,4E,6E)-4-methylocta-2,4,6-trienedial
acid-base catalysis in the CCD8 catalytic cycle and existence of an essential cysteine residue in the CCD8 active site, two-step kinetic mechanism
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
PATHWAY SOURCE
PATHWAYS
-
-
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
SYSTEMATIC NAME
IUBMB Comments
all-trans-10'-apo-beta-carotenal:O2 oxidoreductase (13,14-cleaving)
Requires Fe2+. The enzyme from the plant Arabidopsis thaliana also catalyses EC 1.13.11.69, carlactone synthase, 10-fold faster.
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
SUBSTRATE
PRODUCT
REACTION DIAGRAM
ORGANISM
UNIPROT
COMMENTARY
(Substrate)
(Substrate)
LITERATURE
(Substrate)
(Substrate)
COMMENTARY
(Product)
(Product)
LITERATURE
(Product)
(Product)
Reversibility
r=reversible
ir=irreversible
?=not specified
r=reversible
ir=irreversible
?=not specified
all-trans-10'-apo-beta-carotenal + O2
13-apo-beta-carotenone + (2E,4E,6E)-4-methylocta-2,4,6-trienedial
all-trans-10'-apo-beta-carotenal + O2
13-apo-beta-carotenone + (2E,4E,6E)-4-methylocta-2,4,6-trienedial
-
-
-
?
all-trans-10'-apo-beta-carotenal + O2
13-apo-beta-carotenone + (2E,4E,6E)-4-methylocta-2,4,6-trienedial
-
-
-
?
all-trans-10'-apo-beta-carotenal + O2
13-apo-beta-carotenone + (2E,4E,6E)-4-methylocta-2,4,6-trienedial
-
-
-
-
?
all-trans-10'-apo-beta-carotenal + O2
13-apo-beta-carotenone + ?
-
-
-
-
?
all-trans-10'-apo-beta-carotenol + O2
13-apo-beta-carotenone + ?
-
-
-
-
?
additional information
?
-
enzyme additionally catalyzes the conversion of 9-cis-10'-apo-beta-carotenal to carlactone and (2E,4E,6E)-7-hydroxy-4-methylhepta-2,4,6-trienal, EC 1.13.11.69. The formation of carlactone is about 10fold faster than the formation of 13-apo-beta-carotenone
-
-
?
additional information
?
-
CCD8-dependent conversion of beta-apo-10beta-carotenal to unstable carlactone, reaction of EC 1.13.11.69
-
-
?
additional information
?
-
-
no substrate: 10'-apo-beta-carotenone, 12'-apo-beta-carotenal, 8'-apo-beta-carotenal, rosafluene dialdehyde, 10'-apo-lycopenal, (3R)-3-hydroxy-10'-apo-beta-carotenal, lycopene, beta-carotene, zeaxanthin, lutein and neoxanthin
-
-
?
additional information
?
-
-
enzyme additionally catalyzes the conversion of 9-cis-10'-apo-beta-carotenal to carlactone and (2E,4E,6E)-7-hydroxy-4-methylhepta-2,4,6-trienal, EC 1.13.11.69. The formation of carlactone is about 10fold faster than the formation of 13-apo-beta-carotenone
-
-
?
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
NATURAL SUBSTRATE
NATURAL PRODUCT
REACTION DIAGRAM
ORGANISM
UNIPROT
COMMENTARY
(Substrate)
(Substrate)
LITERATURE
(Substrate)
(Substrate)
COMMENTARY
(Product)
(Product)
LITERATURE
(Product)
(Product)
REVERSIBILITY
r=reversible
ir=irreversible
?=not specified
r=reversible
ir=irreversible
?=not specified
all-trans-10'-apo-beta-carotenal + O2
13-apo-beta-carotenone + (2E,4E,6E)-4-methylocta-2,4,6-trienedial
all-trans-10'-apo-beta-carotenal + O2
13-apo-beta-carotenone + (2E,4E,6E)-4-methylocta-2,4,6-trienedial
-
-
-
?
all-trans-10'-apo-beta-carotenal + O2
13-apo-beta-carotenone + (2E,4E,6E)-4-methylocta-2,4,6-trienedial
-
-
-
?
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
INHIBITOR
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
IMAGE
(2E)-3-(3,4-dimethoxyphenyl)-N-hydroxyprop-2-enamide
over 95% inhibition at 0.1 mM
(2E)-N-benzyl-N-hydroxy-3,7-dimethylocta-2,6-dienamide
52% inhibition at 0.1 mM
(2E)-N-hydroxy-3-(4-methoxyphenyl)prop-2-enamide
over 95% inhibition at 0.1 mM
(2E,4E)-N-benzyl-N-hydroxy-5,9-dimethyldeca-2,4,8-trienamide
47% inhibition at 0.1 mM
(2E,4E)-N-hydroxy-3-methyl-5-(2,6,6-trimethylcyclohex-1-en-1-yl)penta-2,4-dienamide
over 95% inhibition at 0.1 mM
2-(2H-1,3-benzodioxol-5-yl)-N-[(4-fluorophenyl)methyl]-N-hydroxyacetamide
over 95% inhibition at 0.1 mM
2-(3,4-dimethoxyphenyl)-N-[(4-fluorophenyl)methyl]-N-hydroxyacetamide
over 95% inhibition at 0.1 mM
3-(3,4-dimethoxyphenyl)-N-hydroxy-N-octylpropanamide
over 95% inhibition at 0.1 mM
3-(3,4-dimethoxyphenyl)-N-hydroxypropanamide
78% inhibition at 0.1 mM
3-amino-N-benzyl-N-hydroxybenzamide
over 95% inhibition at 0.1 mM
N-benzyl-2-(3,4-dimethoxyphenyl)-N-hydroxyacetamide
over 95% inhibition at 0.1 mM
N-benzyl-3-chloro-N-hydroxybenzamide
over 95% inhibition at 0.1 mM
N-benzyl-N-hydroxy-2-(4-hydroxyphenyl)acetamide
over 95% inhibition at 0.1 mM
N-benzyl-N-hydroxy-3,4-dimethoxybenzamide
over 95% inhibition at 0.1 mM
N-benzyl-N-hydroxy-3-(4-methoxyphenyl)propanamide
over 95% inhibition at 0.1 mM
N-benzyl-N-hydroxy-4-methoxybenzamide
over 95% inhibition at 0.1 mM
N-hydroxy-3-(4-methoxyphenyl)-N-octylpropanamide
over 95% inhibition at 0.1 mM
N-hydroxy-3-(4-methoxyphenyl)propanamide
over 95% inhibition at 0.1 mM
N-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-N-hydroxy-2-(4-methoxyphenyl)acetamide
70% inhibition at 0.1 mM
N-[(4-fluorophenyl)methyl]-N-hydroxy-2-(4-hydroxyphenyl)acetamide
over 95% inhibition at 0.1 mM
N-[(4-fluorophenyl)methyl]-N-hydroxy-2-(4-methoxyphenyl)acetamide
over 95% inhibition at 0.1 mM
N-[(4-fluorophenyl)methyl]-N-hydroxy-3,4-dimethoxybenzamide
over 95% inhibition at 0.1 mM
N-[(4-fluorophenyl)methyl]-N-hydroxy-3-(4-methoxyphenyl)propanamide
over 95% inhibition at 0.1 mM
N-[(4-fluorophenyl)methyl]-N-hydroxy-4-methoxybenzamide
over 95% inhibition at 0.1 mM
N1-[(4-fluorophenyl)methyl]-N1-hydroxy-N4-[(4-methoxyphenyl)methyl]butanediamide
-
sodium 3-[hydroxy[(4-methoxyphenyl)acetyl]amino]propanoate
47% inhibition at 0.1 mM
sodium 3-[hydroxy[(naphthalen-2-yl)acetyl]amino]propanoate
92% inhibition at 0.1 mM
additional information
AtCCD8 is inhibited in a time-dependent fashion by hydroxamic acids N-[(4-fluorophenyl)methyl]-N-hydroxy-2-(4-hydroxyphenyl)acetamide, N-[(4-fluorophenyl)methyl]-N-hydroxy-2-(4-methoxyphenyl)acetamide, N-benzyl-2-(3,4-dimethoxyphenyl)-N-hydroxyacetamide and 2-(3,4-dimethoxyphenyl)-N-[(4-fluorophenyl)methyl]-N-hydroxyacetamide with over 95% inhibition at 0.10 mM, hydroxamic acids acids N-[(4-fluorophenyl)methyl]-N-hydroxy-2-(4-hydroxyphenyl)acetamide, N-[(4-fluorophenyl)methyl]-N-hydroxy-2-(4-methoxyphenyl)acetamide, N-benzyl-2-(3,4-dimethoxyphenyl)-N-hydroxyacetamide and 2-(3,4-dimethoxyphenyl)-N-[(4-fluorophenyl)methyl]-N-hydroxyacetamide cause a shoot branching phenotype in Arabidopsis thaliana. Selective inhibition of CCD8 is observed using hydroxamic acids N-hydroxy-3-(4-methoxyphenyl)propanamide and N-[(4-fluorophenyl)methyl]-N-hydroxy-3-(4-methoxyphenyl)propanamide. No inhibition by N1-[(4-fluorophenyl)methyl]-N1-hydroxy-N4-[(4-methoxyphenyl)methyl]butanediamide
-
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
KM VALUE [mM]
SUBSTRATE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
IMAGE
additional information
additional information
two-step kinetic mechanism, pre-steady-state kinetic analysis
-
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
TEMPERATURE OPTIMUM
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
ORGANISM
COMMENTARY
LITERATURE
UNIPROT
SEQUENCE DB
SOURCE
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
SOURCE TISSUE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
SOURCE
additional information
enzyme expression in the root is sufficient for wild-type shoot branching levels. Strong expression in root tips
brenda
-
subterranean shoot named spider, high expression level of CCD8
brenda
additional information
expression of gene is widely distributed, but at low level
brenda
additional information
CsCCD8 is highly expressed in quiescent axillary buds and decapitation dramatically reduced its expression levels. CsCCD8 expression is higher in the newly developed vascular tissue of axillary buds compared to the vascular tissue of the apical bud. Expression levels in the apical bud are much reduced in comparison with the expression levels in the quiescent axillary buds, suggesting that the levels of CsCCD8 are reduced during the sprouting process. Tissue expression analysis, overview
brenda
additional information
-
developmental expression of CCD8 in different tissues of the parasite, overview
brenda
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
GENERAL INFORMATION
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
evolution
occurrence of duplication in CCD4 genes that evolved into two new genes CCD7, EC 1.13.11.68, and CCD8. The site-specific profile and coefficient of type-I functional divergences reveals critical amino acid residues, leading to subgroup-specific functional evolution after their phylogenetic diversification
malfunction
metabolism
biosynthesis of strigolactones requires the action of two CCD enzymes, CCD7 (EC 1.13.11.68) and CCD8, which act sequentially on 9-cis-beta-carotene, strigolactone biosynthesis pathway from all-trans-beta-carotene to ent-2'-epi-5-deoxystrigol, overview
physiological function
additional information
in silico analysis, structure homology modeling, molecular modeling, dynamic simulation and structure comparisons of Arabidopsis thaliana carotenoid cleavage dioxygenases, overview
malfunction
-
using a PpCCD8 knockout mutant, it is shown that PpCCD8 is involved in strigolactone biosynthesis and regulates the branching of filament and colony extension. In wild-type Physcomitrella patens, secreted strigolactones are directly involved in the regulation of colony extension in response to internal cues or population density
malfunction
-
gene silencing of CCD8 in Phelipanche aegyptiaca by tobacco rattle virus system retards the parasite development on the host. Transient knockdown of PaCCD8 inhibits tubercle development and the infestation process in host plants. The number of parasite tubercles attached to the roots of host plants treated with TRV:PaCCD7, TRV:PaCCD8, or a mixture of TRV:PaCCD7 and TRV:PaCCD8 is significantly reduced by 95% as compared to control plants
malfunction
the biochemical basis of the shoot branching phenotype is due to inhibition of enzyme CCD8
physiological function
-
coexpression of the enzyme, CCD8, and carotenoid-9',10'-cleaving dioxygenase CCD7, EC 1.13.11.71, in Escherichia coli results in production of 13-apo-beta-carotenone. The sequential cleavages of beta-carotene by CCD7 and CCD8 are likely the initial steps in the synthesis of a carotenoid-derived signaling molecule that is necessary for the regulation lateral branching
physiological function
enzyme is involved in regulation of low phosphate stress responses. Mutants show lower anthocyanin content and longer primary root length. Mutant plants also display altered root architecture such as increased root-to-shoot ratio, lower lateral root number and root hair density compared with wild-type plants under low phosphate stress. Higher total phosphate contents are detected in shoots and roots of mutant plants than those of wild-type plants when subjected to low phosphate stress, which is associated, at least in part, with increase in expression of WRKY75 as well as AtPT1 and AtPT2 genes encoding high-affinity phosphate transporters
physiological function
gene disruption mutant reveals a modest increase in branching that contrasts with prominent pleiotropic changes that include marked reduction in stem diameter, reduced elongation of internodes, independent of carbon supply, and a pronounced delay in development of the centrally important, nodal system of adventitious roots
physiological function
loss-of-function mutants exhibit a significant decrease in petiole length and are highly branched. The axillary buds, which are typically delayed in growth in wild-type plants, grow out to produce leaves and inflorescences. The mutant plant have smaller rosette diameters due to a decrease in the lengths of petioles and leaf blades compared with wild-type plants. The phenotypes contribute to the bushy appearance of the mutants. The double mutant, additionally lacking carotenoid-9',10'-cleaving dioxygenase activity, EC 1.13.11.71, is phenotypically indistinguishable from either single mutant, indicating an interaction consistent with both genes functioning in the same pathway. Both classes of plants show a slight increase in inflorescence number compared with wild type
physiological function
mutations in the MAX4 gene of Arabidopsis result in increased and auxin-resistant bud growth. Increased branching in max4 shoots is restored to wild type by grafting to wild-type rootstocks, suggesting that MAX4 is required to produce a mobile branch-inhibiting signal, acting downstream of auxin
physiological function
reduction of enzyme expression by RNAi correlates with an increase in branch development and delayed senescence
physiological function
biosynthesis of strigolactones requires the action of two CCD enzymes, CCD7 (EC 1.13.11.68) and CCD8, which act sequentially on 9-cis-beta-carotene
physiological function
-
important role of the strigolactone associated gene PaCCD8 in the parasite life cycle, and roles of CCD7 and CCD8 enzymes in the biosynthesis of strigolactones
physiological function
two carotenoid cleavage dioxygenases, CCD7 and CCD8, are involved in strigolactones biosynthesis. Involvement of the branching enzymes CCD7 and CCD8 in the control of bud sprouting and apical dominance. CsCCD7 and CsCCD8 expression show some overlapping, although they are not identical
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
UNIPROT
ENTRY NAME
ORGANISM
NO. OF AA
NO. OF TRANSM. HELICES
MOLECULAR WEIGHT[Da]
SOURCE
SEQUENCE
LOCALIZATION PREDICTION
The reliability class of the localization prediction ranges from 1 (very reliable) to 5 (not reliable).
The reliability class of the localization prediction ranges from 1 (very reliable) to 5 (not reliable). CCD8B_ORYSJ
569
0
61984
Swiss-Prot
Chloroplast (Reliability: 3)
CCD8_ARATH
570
0
63957
Swiss-Prot
Chloroplast (Reliability: 5)
A0A2H4G7S3_DUNSA
576
0
63353
TrEMBL
Chloroplast (Reliability: 4)
A0A2G9GZ39_9LAMI
556
0
61823
TrEMBL
Chloroplast (Reliability: 3)
A0A1L5JJ05_CAMSI
528
0
60311
TrEMBL
Secretory Pathway (Reliability: 1)
A0A251VH23_HELAN
553
0
61394
TrEMBL
Chloroplast (Reliability: 3)
C4PJN4_MAIZE
572
0
62407
TrEMBL
other Location (Reliability: 3)
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
PROTEIN VARIANTS
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
additional information
additional information
enzyme is able to complement a CCD8 mutation in Arabidopsis thaliana
additional information
-
coexpression of the enzyme, CCD8, and carotenoid-9',10'-cleaving dioxygenase CCD7, EC 1.13.11.71, in Escherichia coli results in production of 13-apo-beta-carotenone. The sequential cleavages of beta-carotene by CCD7 and CCD8 are likely the initial steps in the synthesis of a carotenoid-derived signaling molecule that is necessary for the regulation lateral branching
additional information
-
gene silencing of CCD8 in Phelipanche aegyptiaca by tobacco rattle virus system, parasitic PaCCD8 gene is silenced in Phelipanche aegyptiaca using a trans-silencing approach in Nicotiana benthamiana. Transient knockdown of PaCCD8 inhibits tubercle development and the infestation process in host plants
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
PURIFICATION (Commentary)
ORGANISM
UNIPROT
LITERATURE
recombinant His6-tagged AtCCD8 lacking the first 168 bp from Escherichia coli strain BL21 by nickel affinity chromatography
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
CLONED (Commentary)
ORGANISM
UNIPROT
LITERATURE
expression in Escherichia coli
gene ccd8, quantitative real-time and RT-PCR enzyme expression analysis
-
gene ccd8, recombinant expression of N-terminally His6-tagged AtCCD8 lacking the first 168 bp, corresponding to a chloroplast transit peptide, in Escherichia coli strain BL21
gene ccd8, sequence comparisons
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
EXPRESSION
ORGANISM
UNIPROT
LITERATURE
decapitation dramatically reduces the high CsCCD8 expression levels in quiescent axillary buds
enzyme is upregulated in the root eleongation zone following 24 h auxin treatment, and hypocotyl, and this is not required for the inhibition of shoot branching
no evidence is found for auxin-induced upregulation of enzyme expression in nodal tissue
Please wait a moment until the data is sorted. This message will disappear when the data is sorted.
REF.
AUTHORS
TITLE
JOURNAL
VOL.
PAGES
YEAR
ORGANISM (UNIPROT)
PUBMED ID
SOURCE
Jiang, L.; Jian, H.; Qian, J.; Sun, Z.; Wei, Z.; Chen, X.; Cao, S.
MAX4 gene is involved in the regulation of low inorganic phosphate stress responses in Arabidopsis thaliana
Acta Physiol. Plant.
33
867-875
2011
Arabidopsis thaliana (Q8VY26)
-
brenda
Alder, A.; Holdermann, I.; Beyer, P.; Al-Babili, S.
Carotenoid oxygenases involved in plant branching catalyse a highly specific conserved apocarotenoid cleavage reaction
Biochem. J.
416
289-296
2008
Arabidopsis thaliana, Oryza sativa, Pisum sativum
brenda
Sorefan, K.; Booker, J.; Haurogne, K.; Goussot, M.; Bainbridge, K.; Foo, E.; Chatfield, S.; Ward, S.; Beveridge, C.; Rameau, C.; Leyser, O.
MAX4 and RMS1 are orthologous dioxygenase-like genes that regulate shoot branching in Arabidopsis and pea
Genes Dev.
17
1469-1474
2003
Arabidopsis thaliana (Q8VY26)
brenda
Schwartz, S.H.; Qin, X.; Loewen, M.C.
The biochemical characterization of two carotenoid cleavage enzymes from Arabidopsis indicates that a carotenoid-derived compound inhibits lateral branching
J. Biol. Chem.
279
46940-46945
2004
Arabidopsis thaliana
brenda
Ledger, S.E.; Janssen, B.J.; Karunairetnam, S.; Wang, T.; Snowden, K.C.
Modified CAROTENOID CLEAVAGE DIOXYGENASE8 expression correlates with altered branching in kiwifruit (Actinidia chinensis)
New Phytol.
188
803-813
2010
Actinidia chinensis (E3T3A2)
brenda
Bainbridge, K.; Sorefan, K.; Ward, S.; Leyser, O.
Hormonally controlled expression of the Arabidopsis MAX4 shoot branching regulatory gene
Plant J.
44
569-580
2005
Arabidopsis thaliana (Q8VY26)
brenda
Auldridge, M.E.; Block, A.; Vogel, J.T.; Dabney-Smith, C.; Mila, I.; Bouzayen, M.; Magallanes-Lundback, M.; DellaPenna, D.; McCarty, D.R.; Klee, H.J.
Characterization of three members of the Arabidopsis carotenoid cleavage dioxygenase family demonstrates the divergent roles of this multifunctional enzyme family
Plant J.
45
982-993
2006
Arabidopsis thaliana (Q8VY26)
brenda
Guan, J.C.; Koch, K.E.; Suzuki, M.; Wu, S.; Latshaw, S.; Petruff, T.; Goulet, C.; Klee, H.J.; McCarty, D.R.
Diverse roles of strigolactone signaling in maize architecture and the uncoupling of a branching-specific subnetwork
Plant Physiol.
160
1303-1317
2012
Zea mays (C4PJN4)
brenda
Alder, A.; Jamil, M.; Marzorati, M.; Bruno, M.; Vermathen, M.; Bigler, P.; Ghisla, S.; Bouwmeester, H.; Beyer, P.; Al-Babili, S.
The path from beta-carotene to carlactone, a strigolactone-like plant hormone
Science
335
1348-1351
2012
Pisum sativum, Arabidopsis thaliana (Q8VY26)
brenda
Proust, H.; Hoffmann, B.; Xie, X.; Yoneyama, K.; Schaefer, D.G.; Yoneyama, K.; Nogue, F.; Rameau, C.
Strigolactones regulate protonema branching and act as a quorum sensing-like signal in the moss Physcomitrella patens
Development
138
1531-1539
2011
Physcomitrium patens
brenda
Rubio-Moraga, A.; Ahrazem, O.; Perez-Clemente, R.M.; Gomez-Cadenas, A.; Yoneyama, K.; Lopez-Raez, J.A.; Molina, R.V.; Gomez-Gomez, L.
Apical dominance in saffron and the involvement of the branching enzymes CCD7 and CCD8 in the control of bud sprouting
BMC Plant Biol.
14
171
2014
Crocus sativus (A0A075IBX5 AND A0A075IGQ2)
brenda
Harrison, P.J.; Newgas, S.A.; Descombes, F.; Shepherd, S.A.; Thompson, A.J.; Bugg, T.D.
Biochemical characterization and selective inhibition of beta-carotene cis-trans isomerase D27 and carotenoid cleavage dioxygenase CCD8 on the strigolactone biosynthetic pathway
FEBS J.
282
3986-4000
2015
Arabidopsis thaliana (Q8VY26)
brenda
Priya, R.; Sneha, P.; Rivera Madrid, R.; Doss, C.G.P.; Singh, P.; Siva, R.
Molecular modeling and dynamic simulation of Arabidopsis thaliana carotenoid cleavage dioxygenase gene a comparison with Bixa orellana and Crocus sativus
J. Cell. Biochem.
118
2712-2721
2017
Arabidopsis thaliana (Q8VY26)
brenda
Aly, R.; Dubey, N.; Yahyaa, M.; Abu-Nassar, J.; Ibdah, M.
Gene silencing of CCD7 and CCD8 in Phelipanche aegyptiaca by tobacco rattle virus system retarded the parasite development on the host
Plant Signal. Behav.
9
e29376
2014
Phelipanche aegyptiaca
brenda
Select items on the left to see more content.
EXTERNAL LINKS (specific for EC-Number 1.13.11.70)
html completed
Use of this online version of BRENDA is free under the CC BY 4.0 license. See terms of use for full details.
Release 2023.1 (January 2023)
About BRENDA
Social media
Help
Survey
Download
Contribution
Legal
Curated at
Member of
