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Information on EC 2.3.1.75 - long-chain-alcohol O-fatty-acyltransferase and Organism(s) Simmondsia chinensis and UniProt Accession Q9XGY6

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EC Tree
IUBMB Comments
Transfers saturated or unsaturated acyl residues of chain-length C18 to C20 to long-chain alcohols, forming waxes. The best acceptor is cis-icos-11-en-1-ol.
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This record set is specific for:
Simmondsia chinensis
UNIPROT: Q9XGY6
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Word Map
The taxonomic range for the selected organisms is: Simmondsia chinensis
The expected taxonomic range for this enzyme is: Bacteria, Eukaryota
Synonyms
acyl-coa:retinol acyltransferase, wax synthase, wax ester synthase, awat2, awat1, wax ester synthase/diacylglycerol acyltransferase, atfa1, wax ester synthase/acyl-coenzyme a:diacylglycerol acyltransferase, maqu_0168, acyl-coa wax alcohol acyltransferases, more
SYNONYM
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
fatty acyl-coenzyme A:fatty alcohol acyltransferase
-
acyl-CoA:alcohol transacylase
-
-
acyltransferase, long-chain alcohol
-
-
-
-
wax ester synthase
-
-
wax synthase
wax-ester synthase
-
-
-
-
REACTION TYPE
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
Acyl group transfer
-
-
-
-
PATHWAY SOURCE
PATHWAYS
-
-, -, -, -
SYSTEMATIC NAME
IUBMB Comments
acyl-CoA:long-chain-alcohol O-acyltransferase
Transfers saturated or unsaturated acyl residues of chain-length C18 to C20 to long-chain alcohols, forming waxes. The best acceptor is cis-icos-11-en-1-ol.
CAS REGISTRY NUMBER
COMMENTARY hide
64060-40-8
-
SUBSTRATE
PRODUCT                       
REACTION DIAGRAM
ORGANISM
UNIPROT
COMMENTARY
(Substrate) hide
LITERATURE
(Substrate)
COMMENTARY
(Product) hide
LITERATURE
(Product)
Reversibility
r=reversible
ir=irreversible
?=not specified
eicosenoyl-CoA + octadecenol
octadecenyl eicosenoate + CoA
show the reaction diagram
best substrates
-
-
?
acyl-CoA + a long-chain alcohol
CoA + a long-chain ester
show the reaction diagram
-
-
-
-
?
cis-11-eicosenol + acetyl-CoA
cis-11-eicosenyl acetate + CoA
show the reaction diagram
-
-
-
-
?
eicosanoyl-CoA + cis-11-eicosenol
cis-11-eicosenyl eicosanoate + CoA
show the reaction diagram
-
cis-11-eicosenol is the best acceptor
-
-
?
eicosanoyl-CoA + cis-13-eicosenol
cis-13-eicosenyl eicosanoate + CoA
show the reaction diagram
-
-
-
-
?
eicosanoyl-CoA + cis-9-octadecenol
cis-9-octadecenyl eicosanoate + CoA
show the reaction diagram
-
-
-
-
?
eicosanoyl-CoA + decanol
decanyl eicosanoate + CoA
show the reaction diagram
-
low activity
-
-
?
eicosanoyl-CoA + docosanol
docosanyl eicosanoate + CoA
show the reaction diagram
-
low activity
-
-
?
eicosanoyl-CoA + dodecanol
dodecanyl eicosanoate + CoA
show the reaction diagram
-
-
-
-
?
eicosanoyl-CoA + eicosanol
eicosanyl eicosanoate + CoA
show the reaction diagram
-
low activity
-
-
?
eicosanoyl-CoA + hexadecanol
hexadecanyl eicosanoate + CoA
show the reaction diagram
-
-
-
-
?
eicosanoyl-CoA + octadecanol
octadecanyl eicosanoate + CoA
show the reaction diagram
-
low activity
-
-
?
eicosanoyl-CoA + tetradecanol
tetradecanyl eicosanoate + CoA
show the reaction diagram
-
-
-
-
?
eicosenoyl-CoA + docosenol
docosenyl eicosenoate + CoA
show the reaction diagram
eicosenoyl-CoA + dodecanol
dodecyl eicosenoate + CoA
show the reaction diagram
-
high activity
-
-
?
eicosenoyl-CoA + hexadecanol
hexadecanyl eicosenate + CoA
show the reaction diagram
-
high activity
-
-
?
eicosenoyl-CoA + tetradecanol
tetradecyl eicosenoate + CoA
show the reaction diagram
-
high activity
-
-
?
linoleoyl-CoA + dodecanol
dodecyl linoleate + CoA
show the reaction diagram
-
high activity
-
-
?
linoleoyl-CoA + hexadecanol
hexadecanyl linoleate + CoA
show the reaction diagram
-
high activity
-
-
?
linoleoyl-CoA + tetradecanol
tetradecyl linoleate + CoA
show the reaction diagram
myristoyl-CoA + docosenol
docosenyl myristate + CoA
show the reaction diagram
-
-
-
-
?
myristoyl-CoA + eicosenol
eicosenyl myristate + CoA
show the reaction diagram
-
highest activity
-
-
?
myristoyl-CoA + hexadecanol
hexadecanyl myristate + CoA
show the reaction diagram
-
high activity
-
-
?
myristoyl-CoA + hexadecenol
hexadecenyl myristate + CoA
show the reaction diagram
-
high activity
-
-
?
myristoyl-CoA + linolenyl alcohol
linolenoyl myristate + CoA
show the reaction diagram
-
high activity
-
-
?
myristoyl-CoA + linoleyl alcohol
linoleoyl myristate + CoA
show the reaction diagram
-
high activity
-
-
?
myristoyl-CoA + octadecanol
octadecyl myristate + CoA
show the reaction diagram
-
high activity
-
-
?
myristoyl-CoA + octadecenol
octadecenyl myristate + CoA
show the reaction diagram
-
high activity
-
-
?
myristoyl-CoA + phytol
phytyl myristate + CoA
show the reaction diagram
-
-
-
-
?
myristoyl-CoA + tetracosenol
tetracosenyl myristate + CoA
show the reaction diagram
-
-
-
-
?
octadecenoyl-CoA + dodecanol
dodecanyl octadecanoate + CoA
show the reaction diagram
-
-
-
-
ir
oleoyl-CoA + oleyl alcohol
oleyl oleate + CoA
show the reaction diagram
-
-
-
-
?
oleoyl-CoA + tetradecanol
tetradecyl oleate + CoA
show the reaction diagram
-
high activity
-
-
?
palmitoyl-CoA + eicosenol
eicosenyl palmitate + CoA
show the reaction diagram
-
high activity
-
-
?
palmitoyl-CoA + hexadecanol
hexadecanyl palmitate + CoA
show the reaction diagram
-
high activity
-
-
?
palmitoyl-CoA + hexadecenol
hexadecenyl palmitate + CoA
show the reaction diagram
-
-
-
-
?
palmitoyl-CoA + octadecanol
octadecyl palmitate + CoA
show the reaction diagram
-
high activity
-
-
?
palmitoyl-CoA + octadecenol
octadecenyl palmitate + CoA
show the reaction diagram
-
high activity
-
-
?
stearoyl-CoA + tetradecanol
tetradecyl stearate + CoA
show the reaction diagram
-
high activity
-
-
?
additional information
?
-
NATURAL SUBSTRATE
NATURAL PRODUCT
REACTION DIAGRAM
ORGANISM
UNIPROT
COMMENTARY
(Substrate) hide
LITERATURE
(Substrate)
COMMENTARY
(Product) hide
LITERATURE
(Product)
REVERSIBILITY
r=reversible
ir=irreversible
?=not specified
acyl-CoA + a long-chain alcohol
CoA + a long-chain ester
show the reaction diagram
-
-
-
-
?
cis-11-eicosenol + acetyl-CoA
cis-11-eicosenyl acetate + CoA
show the reaction diagram
-
-
-
-
?
COFACTOR
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
ATP
-
activation
CTP
-
activation
UTP
-
activation
METALS and IONS
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
additional information
-
no influence of NaCl or KCl up to 20 mM
INHIBITOR
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
bovine serum albumin
-
above 5 mg/ml
-
Polyvinylpyrrolidone
-
slight inhibition
ACTIVATING COMPOUND
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
bovine serum albumin
-
GTP
-
activation
pH OPTIMUM
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
7
-
the activity of the enzyme gradually increases with the raise of buffer pH reaching the maximum at pH around 7.0
additional information
TEMPERATURE OPTIMUM
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
ORGANISM
COMMENTARY hide
LITERATURE
UNIPROT
SEQUENCE DB
SOURCE
SOURCE TISSUE
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
SOURCE
LOCALIZATION
ORGANISM
UNIPROT
COMMENTARY hide
GeneOntology No.
LITERATURE
SOURCE
UNIPROT
ENTRY NAME
ORGANISM
NO. OF AA
NO. OF TRANSM. HELICES
MOLECULAR WEIGHT[Da]
SOURCE
SEQUENCE
LOCALIZATION PREDICTION?
WAXS1_SIMCH
352
7
40157
Swiss-Prot
other Location (Reliability: 2)
MOLECULAR WEIGHT
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
30000
x * 30000, SDS-PAGE
40000
gel filtration
additional information
SUBUNIT
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
?
x * 30000, SDS-PAGE
PROTEIN VARIANTS
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
additional information
TEMPERATURE STABILITY
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
25
-
reduced stability
50
-
10 min, complete inactivation
additional information
-
no improvement of heat-stability by polyvinylpyrrolidone
GENERAL STABILITY
ORGANISM
UNIPROT
LITERATURE
no improvement of heat-stability by polyvinylpyrrolidone
-
wax esters formation is not observed in citrate buffer with pH below 5.5. The enzyme activity at pH 6.0 is higher in citrate buffer than in p-buffer
-
STORAGE STABILITY
ORGANISM
UNIPROT
LITERATURE
0°C, fairly stable
-
4°C, 2-3 h stable
-
PURIFICATION (Commentary)
ORGANISM
UNIPROT
LITERATURE
CLONED (Commentary)
ORGANISM
UNIPROT
LITERATURE
cloning of cDNA, DNA sequence analysis, construction of plasmid to express the cDNA in transgenic Arabidopsis thaliana plants
expressed in Saccharomyces cerevisiae quadruple mutant strain H1246
-
expressed in seeds of Arabidopsis thaliana and Camelina sativa
-
APPLICATION
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
agriculture
transgenic plants expressing the enzyme allow the production of long-chain liquid waxes at reasonable cost for use in commercial applications
REF.
AUTHORS
TITLE
JOURNAL
VOL.
PAGES
YEAR
ORGANISM (UNIPROT)
PUBMED ID
SOURCE
Wu, X.Y.; Moreau, R.A.; Stumpf, P.K.
Studies of biosynthesis of waxes by developing jojoba seed: III. Biosynthesis of wax esters from acetyl-CoA and long-chain alcohols
Lipids
16
897-902
1981
Simmondsia chinensis
-
Manually annotated by BRENDA team
Garver, W.S.; Kemp, J.D.; Kuehn, G.D.
A high-performance liquid chromatography-based radiometric assay for acyl-CoA:alcohol transacylase from jojoba
Anal. Biochem.
207
335-340
1992
Simmondsia chinensis
Manually annotated by BRENDA team
Lardizabal, K.D.; Metz, J.G.; Sakamoto, T.; Hutton, W.C.; Pollard, M.R.; Lassner, M.W.
Purification of a jojoba embryo wax synthase, cloning of its cDNA, and production of high levels of wax in seeds of transgenic Arabidopsis
Plant Physiol.
122
645-655
2000
Simmondsia chinensis (Q9XGY6), Simmondsia chinensis
Manually annotated by BRENDA team
Miklaszewska, M.; Banas, A.
Biochemical characterization and substrate specificity of jojoba fatty acyl-CoA reductase and jojoba wax synthase
Plant Sci.
249
84-92
2016
Simmondsia chinensis
Manually annotated by BRENDA team
Iven, T.; Hornung, E.; Heilmann, M.; Feussner, I.
Synthesis of oleyl oleate wax esters in Arabidopsis thaliana and Camelina sativa seed oil
Plant Biotechnol. J.
14
252-259
2016
Simmondsia chinensis
Manually annotated by BRENDA team