Entry
Name
beta-carotene 3-hydroxylase;
beta-carotene 3,3'-monooxygenase;
CrtZ
Class
Oxidoreductases;
Acting on paired donors, with incorporation or reduction of molecular oxygen;
With reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen into the other donor
BRITE hierarchy
Sysname
beta-carotene,reduced ferredoxin [iron-sulfur] cluster:oxygen 3-oxidoreductase
Reaction(IUBMB)
beta-carotene + 4 reduced ferredoxin [iron-sulfur] cluster + 2 H+ + 2 O2 = zeaxanthin + 4 oxidized ferredoxin [iron-sulfur] cluster + 2 H2O (overall reaction) [RN:
R09747 ];
(1a) beta-carotene + 2 reduced ferredoxin [iron-sulfur] cluster + H+ + O2 = beta-cryptoxanthin + 2 oxidized ferredoxin [iron-sulfur] cluster + H2O [RN:
R07558 ];
(1b) beta-cryptoxanthin + 2 reduced ferredoxin [iron-sulfur] cluster + H+ + O2 = zeaxanthin + 2 oxidized ferredoxin [iron-sulfur] cluster + H2O [RN:
R07559 ]
Reaction(KEGG)
Substrate
Product
zeaxanthin [CPD:
C06098 ];
oxidized ferredoxin [iron-sulfur] cluster [CPD:
C00139 ];
H2O [CPD:
C00001 ];
beta-cryptoxanthin [CPD:
C08591 ]
Comment
Requires ferredoxin and iron(II). Also acts on other carotenoids with a beta-end group. In some species canthaxanthin is the preferred substrate.
History
EC 1.14.15.24 created 2011 as EC 1.14.13.129, transferred 2017 to EC 1.14.15.24
Pathway
ec01110 Biosynthesis of secondary metabolites
Orthology
K15746 beta-carotene 3-hydroxylase
K22492 beta-carotene 3-hydroxylase
K23037 beta-carotene 4-ketolase/3-hydroxylase
Genes
ATH : AT4G25700(BETA-OHASE_1) AT5G52570(BETA-OHASE_2)
CSAT : 104717685 104722390 104725769 104727661 104730850 104761269
EUS : EUTSA_v10014816mg EUTSA_v10025794mg
BRP : 103844746 103861586(BCH) 103863442
BNA : 106347114 106405085 106406976 106421444 106421466 106442750 106442837 106442847
BOE : 106302033 106316293 106323808 106324977
RSZ : 108829383 108829758 108833660 108849036
CIC : CICLE_v10005481mg CICLE_v10022121mg
MINC : 123197303 123210814 123224817
GRA : 105765256 105765515 105800132
GHI : 107890752 107930284 107947054 107947686 107948080 121211198
DZI : 111280864 111287079 111289844 111316378
GMX : 100785541(BCH2) 100802778(BCH4) 100813368(BCH5) 547758(BCH3)
GSJ : 114366981 114370081 114389167 114401551
PVU : PHAVU_004G108900g PHAVU_007G074200g
CCAJ : 109789930 109803178 109803642
APRC : 113867250 113872335
PSAT : 127091743 127128358
LJA : Lj0g3v0299729.1(Lj0g3v0299729.1) Lj2g3v1902110.1(Lj2g3v1902110.1) Lj5g3v1988680.1(Lj5g3v1988680.1)
AHF : 112751851 112802913 112803001
LANG : 109346786 109352248 109354081
PMUM : 103328353 103333723 103337559
PAVI : 110762514 110767732
PDUL : 117619478 117627907
MDM : 103406562 103439793 114825667
PXB : 103953392 103958212 103964324 103966138 103966173
MNT : 21383781 21397383 21406978
CMO : 103482780 103484113(CHXB)
MCHA : 111011750 111025906
CMAX : 111467695 111469080 111482629
CMOS : 111430578 111435746 111449265
CPEP : 111801653 111808948 111809669
HBR : 110643463 110656052 110658181
MESC : 110608652 110616623 110631003
POP : 18106473 7468341 7479294
PEU : 105129097 105133177 105140749
PALZ : 118030260 118037119
JRE : 108982686 109004504 109014502
CILL : 122280762 122311845 122313967
QLO : 115960910 115971862 115972059 115973379
VVI : 100232875(BCH1) 100268009
SLY : 544133(CrtR-b1) 544297(CrtR-b2)
SPEN : 107012889 107023761
SOT : 102580250 102582135 102591473(CHY2)
SSTN : 125860654 125875050
CANN : 107863219 107873401
NTA : 107789701 107809222(CrtR-b1) 107822278(BCH2)
NSY : 104217920 104229839 104235870
NAU : 109212761 109226400 109227191
SIND : 105160437 105166704
OEU : 111391826 111391835 111393339
SSPL : 121783762 121797398 121797620 121805598 121808548
APAN : 127245094 127256396
DCR : 108214828 108217689 108224246
SOE : 110776110 110784117 110794474
MING : 122057800 122075784
PSOM : 113274613 113304779
OSA : 4331460 4336753 4349224
DOSA : Os03t0125100-01(Os03g0125100) Os04t0578400-01(Os04g0578400) Os10t0533500-00(Os10g0533500)
OBR : 102701304 102710199 102719474
OGL : 127765569 127772218 127786112
TDC : 119291805 119303955 119355991 119365127
TAES : 100415846 123046235 123054106 123089378 123108286 123189994
LPER : 127297279 127336447
ZMA : 100273156 100281693 103631225 732775 732825
SITA : 101757118 101770294
PVIR : 120641532 120647483 120683322 120690205
PHAI : 112875902 112898761
MUS : 103970270 103972048 103993184
ZOF : 121969646 121970105 121974781 121975201 122008083 122016290 122039565 122045498
PEQ : 110028272 110031950 110034260
NCOL : 116248927 116252106
SMO : SELMODRAFT_121550 SELMODRAFT_122500 SELMODRAFT_125253 SELMODRAFT_126723 SELMODRAFT_131603 SELMODRAFT_14977
PPP : 112273933 112295550 112295981
VCN : VOLCADRAFT_68369(chyB)
MPP : MICPUCDRAFT_38006(CRTR)
PLF : PANA5342_p10304(crtZ)
PVA : Pvag_pPag30170(crtZ)
PVD : CFBP1590__2677(crtZ)
PSW : LK03_17170 LK03_17805
PPV : NJ69_06670 NJ69_07695
PGG : FX982_03315 FX982_04448
STAX : MC45_05470 MC45_13565
SARI : H5J25_02990 H5J25_17505
PEP : AQ505_11340 AQ505_16675
SMIZ : 4412673_01685 4412673_03992
MUH : HYN43_019580 HYN43_020770
MRUB : DEO27_021535 DEO27_023120
PSEZ : HME7025_02277(crtZ)
SPON : HME9304_02556(crtZ)
POM : MED152_02565(crtZ1) MED152_02665(crtZ3)
AALG : AREALGSMS7_02442 AREALGSMS7_04935
» show all
Taxonomy
Reference
Authors
Sun Z, Gantt E, Cunningham FX Jr
Title
Cloning and functional analysis of the beta-carotene hydroxylase of Arabidopsis thaliana.
Journal
Sequence
Reference
Authors
Fraser PD, Miura Y, Misawa N
Title
In vitro characterization of astaxanthin biosynthetic enzymes.
Journal
Reference
Authors
Fraser PD, Shimada H, Misawa N
Title
Enzymic confirmation of reactions involved in routes to astaxanthin formation, elucidated using a direct substrate in vitro assay.
Journal
Reference
Authors
Bouvier F, Keller Y, d'Harlingue A, Camara B
Title
Xanthophyll biosynthesis: molecular and functional characterization of carotenoid hydroxylases from pepper fruits (Capsicum annuum L.).
Journal
Sequence
Reference
Authors
Linden H
Title
Carotenoid hydroxylase from Haematococcus pluvialis: cDNA sequence, regulation and functional complementation.
Journal
Sequence
Reference
Authors
Zhu C, Yamamura S, Nishihara M, Koiwa H, Sandmann G
Title
cDNAs for the synthesis of cyclic carotenoids in petals of Gentiana lutea and their regulation during flower development.
Journal
Sequence
Reference
Authors
Choi SK, Matsuda S, Hoshino T, Peng X, Misawa N
Title
Characterization of bacterial beta-carotene 3,3'-hydroxylases, CrtZ, and P450 in astaxanthin biosynthetic pathway and adonirubin production by gene combination in Escherichia coli.
Journal
Other DBs
LinkDB
All DBs