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Information on EC 2.8.3.1 - propionate CoA-transferase and Organism(s) Anaerotignum propionicum and UniProt Accession Q9L3F7

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EC Tree
     2 Transferases
         2.8 Transferring sulfur-containing groups
             2.8.3 CoA-transferases
                2.8.3.1 propionate CoA-transferase
IUBMB Comments
Butanoate and lactate can also act as acceptors.
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This record set is specific for:
Anaerotignum propionicum
UNIPROT: Q9L3F7
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Word Map
The taxonomic range for the selected organisms is: Anaerotignum propionicum
The expected taxonomic range for this enzyme is: Bacteria, Archaea, Eukaryota
Synonyms
propionyl-coa transferase, propionate coa-transferase, propionate coa transferase, propionate-coa transferase, propionyl-coa:succinate coa transferase, coenzyme-a transferase, propionate coenzyme a transferase, propionate coenzyme a coa transferase, more
SYNONYM
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
propionate coenzyme A transferase
-
propionate coenzyme-A transferase
-
coenzyme A transferase, propionate
-
-
-
-
coenzyme-A transferase
-
-
propionate CoA transferase
-
-
propionate coenzyme A CoA transferase
-
-
propionate coenzyme A transferase
-
-
propionate coenzyme A-transferase
-
-
-
-
propionate-CoA:lactoyl-CoA transferase
-
-
-
-
propionyl CoA:acetate CoA transferase
-
-
-
-
propionyl-CoA transferase
REACTION TYPE
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
coenzyme A transfer
-
-
-
-
SYSTEMATIC NAME
IUBMB Comments
acetyl-CoA:propanoate CoA-transferase
Butanoate and lactate can also act as acceptors.
CAS REGISTRY NUMBER
COMMENTARY hide
9026-15-7
-
SUBSTRATE
PRODUCT                       
REACTION DIAGRAM
ORGANISM
UNIPROT
COMMENTARY
(Substrate) hide
LITERATURE
(Substrate)
COMMENTARY
(Product) hide
LITERATURE
(Product)
Reversibility
r=reversible
ir=irreversible
?=not specified
acetyl-CoA + propanoate
acetate + propanoyl-CoA
show the reaction diagram
(R)-lactate + propionyl-CoA
propionate + (R)-lactoyl-CoA
show the reaction diagram
-
-
-
-
r
acetyl-CoA + 2-hydroxybutanoate
acetate + 2-hydroxybutyryl-CoA
show the reaction diagram
-
-
-
-
?
acetyl-CoA + 2-hydroxybutyrate
acetate + 2-hydroxybutyryl-CoA
show the reaction diagram
-
-
-
-
?
acetyl-CoA + 3-hydroxybutyrate
acetate + 3-hydroxybutyryl-CoA
show the reaction diagram
-
-
-
-
?
acetyl-CoA + 3-hydroxypropionate
acetate + 3-hydroxypropionyl-CoA
show the reaction diagram
-
-
-
-
?
acetyl-CoA + 3-mercaptopropionate
acetate + 3-mercaptopropionyl-CoA
show the reaction diagram
-
-
-
-
?
acetyl-CoA + acrylate
acetate + acryloyl-CoA
show the reaction diagram
-
-
-
-
?
acetyl-CoA + butanoate
acetate + butanoyl-CoA
show the reaction diagram
-
-
-
-
?
acetyl-CoA + butyrate
acetate + butanoyl-CoA
show the reaction diagram
-
low activity
-
-
?
acetyl-CoA + lactate
pyruvate + acetate + CoA
show the reaction diagram
-
(R)-lactate preferred over (S)-lactate
-
?
acetyl-CoA + oxaloacetate
acetate + oxaloacetyl-CoA
show the reaction diagram
-
-
-
-
?
acetyl-CoA + propanoate
acetate + propanoyl-CoA
show the reaction diagram
acetyl-CoA + propionate
acetate + propanoyl-CoA
show the reaction diagram
-
-
-
-
?
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
acetyl-CoA + propanoate
acetate + propanoyl-CoA
show the reaction diagram
propionate is contained in various fermented foods, is used as an antimicrobial food additive, accumulation of propionate in the blood is caused by propionic acidemia
-
-
?
acetyl-CoA + propanoate
acetate + propanoyl-CoA
show the reaction diagram
acetyl-CoA + propionate
acetate + propanoyl-CoA
show the reaction diagram
-
-
-
-
?
additional information
?
-
-
The wild-type Pct is not able to efficiently convert lactate to lactyl-CoA
-
-
?
COFACTOR
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
INHIBITOR
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
(R)-lactate
-
33% inhibition at 11 mM
(S)-lactate
-
54% inhibition at 11 mM
Acrylate
-
43% inhibition at 11 mM
Butyrate
-
72% inhibition at 11 mM
hydroxylamine
-
rapid and irreversible inactivation
propionate
-
80% inhibition at 11 mM
Sodium borohydride
-
rapid and irreversible inactivation
ACTIVATING COMPOUND
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
propionate
increase in propionate concentration lead to increase of enzyme amount
KM VALUE [mM]
SUBSTRATE
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
0.36
propionate
-
pH 7.0, 25°C
TURNOVER NUMBER [1/s]
SUBSTRATE
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
IMAGE
14.2
propionate
-
pH 7.0, 25°C
SPECIFIC ACTIVITY [µmol/min/mg]
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
0.34
-
substrate propionate
additional information
-
development of propionate-detection systems, overview
pH OPTIMUM
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
pH RANGE
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
6.5 - 8
-
over 90% of maximal activity within this range
TEMPERATURE OPTIMUM
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
TEMPERATURE RANGE
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
25 - 40
-
over 90% of maximal activity within this range
ORGANISM
COMMENTARY hide
LITERATURE
UNIPROT
SEQUENCE DB
SOURCE
UNIPROT
ENTRY NAME
ORGANISM
NO. OF AA
NO. OF TRANSM. HELICES
MOLECULAR WEIGHT[Da]
SOURCE
SEQUENCE
LOCALIZATION PREDICTION?
Q9L3F7_ANAPI
524
0
56552
TrEMBL
-
MOLECULAR WEIGHT
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
224000
-
gel filtration
60000
-
x * 60000, SDS-PAGE
67000
-
4 * 67000, SDS-PAGE
SUBUNIT
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
?
-
x * 60000, SDS-PAGE
tetramer
-
4 * 67000, SDS-PAGE
PROTEIN VARIANTS
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
V193A
-
the Pct540 mutant contains the V193A mutation, and four silent nucleotide exchanges of T78C, T669C, A1125G, T1158C
additional information
-
construction of an engineered enzyme mutant, Pct540, for the generation of poly(3-hydroxybutyrate-co-lactate) and lactyl-CoA endogenously, random mutagenesis, overview. Method optimization and molecular weight of synthesized polymers, overview
STORAGE STABILITY
ORGANISM
UNIPROT
LITERATURE
4°C, for at least 1 month without loss of activity
4°C, in saturated ammonium sulfate, several months
-
PURIFICATION (Commentary)
ORGANISM
UNIPROT
LITERATURE
CLONED (Commentary)
ORGANISM
UNIPROT
LITERATURE
coexpression of the engineered mutant Pct540 from Clostridium propionicum in Escherichia coli strain XL-1 Blue with engineered Pseudomonas sp. MBEL 6-19 polyhydroxyalkanoate synthase 1 mutant, i.e. PhaC1Ps6-19. The expressed wild-type Pct is not able to efficiently convert lactate to lactyl-CoA and exerts an inhibitory effect on cell growth
-
coexpression of the engineered mutant Pct540 from Clostridium propionicum in the engineered Escherichia coli strain JLX7 with engineered Pseudomonas sp. MBEL 6-19 polyhydroxyalkanoate synthase 1 mutant, i.e. PhaC1Ps6-19, production of polylactic acid, flux response analysis, overview. The engineered Escherichia coli strain exerts several knocked out genes, overview
-
expressed in Escherichia coli XL1-Blue cells
-
APPLICATION
ORGANISM
UNIPROT
COMMENTARY hide
LITERATURE
biotechnology
propionate-biosensor, using propionate coenzyme A transferase from Clostridium propionicum and short-chain acyl-CoA oxidase from Arabidopsis thaliana as enzyme electrodes
analysis
amperometric propionate sensor
biotechnology
-
establishing of an on-site monitoring of volatile fatty acids VFA, such as propionate, biosensing system using recombinant propionate CoA transferase and recombinant acyl-CoA oxidase, this system produces hydrogen peroxide in the presence of acetyl-CoA, oxygen, and VFA substrates, which can be quantified by colorimetric methods using peroxidase and dye reagents, e.g., 4-aminobenzoic acid plus 4-aminoantipyrine, overview
synthesis
REF.
AUTHORS
TITLE
JOURNAL
VOL.
PAGES
YEAR
ORGANISM (UNIPROT)
PUBMED ID
SOURCE
Schweiger, G.; Buckel, W.
On the dehydration of (R)-lactate in the fermentation of alanine to propionate by Clostridium propionicum
FEBS Lett.
171
79-84
1984
Anaerotignum propionicum
Manually annotated by BRENDA team
Selmer, T.; Willanzheimer, A.; Hetzel, M.
Propionate CoA-transferase from Clostridium propionicum. Cloning of gene and identification of glutamate 324 at the active site
Eur. J. Biochem.
269
372-380
2002
Anaerotignum propionicum
Manually annotated by BRENDA team
Rajashekhara, E.; Hosoda, A.; Sode, K.; Ikenaga, H.; Watanabe, K.
Volatile fatty acid-sensing system involving coenzyme-A transferase
Biotechnol. Prog.
22
334-337
2006
Anaerotignum propionicum
Manually annotated by BRENDA team
Sode, K.; Tsugawa, W.; Aoyagi, M.; Rajashekhara, E.; Watanabe, K.
Propionate sensor using coenzyme-A transferase and acyl-CoA oxidase
Protein Pept. Lett.
15
779-781
2008
Anaerotignum propionicum, Anaerotignum propionicum (Q9L3F7)
Manually annotated by BRENDA team
Yang, T.H.; Kim, T.W.; Kang, H.O.; Lee, S.H.; Lee, E.J.; Lim, S.C.; Oh, S.O.; Song, A.J.; Park, S.J.; Lee, S.Y.
Biosynthesis of polylactic acid and its copolymers using evolved propionate CoA transferase and PHA synthase
Biotechnol. Bioeng.
105
150-160
2010
Anaerotignum propionicum
Manually annotated by BRENDA team
Jung, Y.K.; Kim, T.Y.; Park, S.J.; Lee, S.Y.
Metabolic engineering of Escherichia coli for the production of polylactic acid and its copolymers
Biotechnol. Bioeng.
105
161-171
2010
Anaerotignum propionicum
Manually annotated by BRENDA team
Han, X.; Satoh, Y.; Satoh, T.; Matsumoto, K.; Kakuchi, T.; Taguchi, S.; Dairi, T.; Munekata, M.; Tajima, K.
Chemo-enzymatic synthesis of polyhydroxyalkanoate (PHA) incorporating 2-hydroxybutyrate by wild-type class I PHA synthase from Ralstonia eutropha
Appl. Microbiol. Biotechnol.
92
509-517
2011
Anaerotignum propionicum, Anaerotignum propionicum JCM 1430
Manually annotated by BRENDA team
Park, S.J.; Kang, K.H.; Lee, H.; Park, A.R.; Yang, J.E.; Oh, Y.H.; Song, B.K.; Jegal, J.; Lee, S.H.; Lee, S.Y.
Propionyl-CoA dependent biosynthesis of 2-hydroxybutyrate containing polyhydroxyalkanoates in metabolically engineered Escherichia coli
J. Biotechnol.
165
93-98
2013
Anaerotignum propionicum
Manually annotated by BRENDA team