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Information on EC 2.8.3.1 - propionate CoA-transferase
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2.8.3.1 propionate CoA-transferaseIUBMB Comments
Butanoate and lactate can also act as acceptors.
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Word Map
- 2.8.3.1
- polyhydroxyalkanoate
- propionicum
- copolymer
- eutropha
-
polylactic
- acetoacetyl-coa
- lactyl-coa
- 2-hydroxybutyrate
- megasphaera
- elsdenii
- 3-hydroxypropionate
- 3-hydroxybutyryl-coa
-
pane
-
phac1s
-
2-hydroxyacids
- xl1-blue
- synthesis
- biotechnology
- analysis
The expected taxonomic range for this enzyme is: Bacteria, Eukaryota
Synonyms
CoAT, coenzyme A transferase, propionate, coenzyme-A transferase, PCT, propionate CoA transferase, propionate CoA-transferase, propionate coenzyme A CoA transferase, propionate coenzyme A transferase, propionate coenzyme A-transferase, propionate coenzyme-A transferase, 
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SYNONYM 
ORGANISM
UNIPROT
COMMENTARY 
LITERATURE
CoAT
coenzyme A transferase, propionate
-
-
-
-
PCT
propionate CoA-transferase
propionate coenzyme A transferase
propionate coenzyme A-transferase
-
-
-
-
propionate-CoA:lactoyl-CoA transferase
-
-
-
-
propionyl CoA:acetate CoA transferase
-
-
-
-
propionyl-CoA transferase
propionyl-CoA:succinate CoA transferase
propionyl-CoA transferase
-
-
-
-
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REACTION
REACTION DIAGRAM
COMMENTARY
ORGANISM
UNIPROT
LITERATURE
acetyl-CoA + propanoate = acetate + propanoyl-CoA
-
-
-
-
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REACTION TYPE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
coenzyme A transfer
-
-
-
-
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PATHWAY SOURCE
PATHWAYS
KEGG
MetaCyc
1,2-propanediol biosynthesis from lactate (engineered), 4-aminobutanoate degradation V, acetyl-CoA fermentation to butanoate II, fermentation to 2-methylbutanoate, gallate degradation III (anaerobic), L-glutamate degradation V (via hydroxyglutarate), pyruvate fermentation to propanoate II (acrylate pathway), succinate fermentation to butanoate
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SYSTEMATIC NAME
IUBMB Comments
acetyl-CoA:propanoate CoA-transferase
Butanoate and lactate can also act as acceptors.
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CAS REGISTRY NUMBER
COMMENTARY
9026-15-7
-
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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
3-hydroxybutyryl-CoA + propanoate
?
-
highest rate of reaction with 3-hydroxybutyryl-CoA (100% activity)
-
-
?
acetyl-CoA + 2-hydroxybutanoate
acetate + 2-hydroxybutyryl-CoA
-
-
-
-
?
acetyl-CoA + 3-hydroxypropanoate
acetate + 3-hydroxypropanoyl-CoA
-
-
-
-
?
acetyl-CoA + glycolate
acetate + glycolyl-CoA
-
no activity at 1 mM and 1% activity at 20 mM compared to propanoate
-
-
?
acetyl-CoA + hexanoate
acetate + hexanoyl-CoA
-
4% activity at 1 mM and 21% activity at 20 mM compared to propanoate
-
-
?
acetyl-CoA + isobutyrate
acetate + isobutyryl-CoA
-
isobutyrate is preferentially used as CoA acceptor (34% activity at 1n mM and 100% activity at 20 mM compared to propanoate)
-
-
?
acetyl-CoA + isovalerate
acetate + isovaleryl-CoA
-
2% activity at 1 mM and 6% activity at 20 mM compared to propanoate
-
-
?
acetyl-CoA + lactate
pyruvate + acetate + CoA
-
(R)-lactate preferred over (S)-lactate
-
-
acetyl-CoA + octanoate
acetate + octanoyl-CoA
-
8% activity at 1 mM and 35% activity at 20 mM compared to propanoate
-
-
?
acetyl-CoA + trans-2,3-octenoate
acetate + trans-2,3-octenoyl-CoA
-
1% activity at 1 mM and 5% activity at 20 mM compared to propanoate
-
-
?
acetyl-CoA + trans-2,3-pentenoate
acetate + trans-2,3-pentenoyl-CoA
-
5% activity at 1 mM and 34% activity at 20 mM compared to propanoate
-
-
?
acetyl-CoA + valerate
acetate + valeryl-CoA
-
14% activity at 1 mM and 41% activity at 20 mM compared to propanoate
-
-
?
acrylate + acrylyl-CoA
acetate + propionyl-CoA
-
69% activity compared to propionate
-
-
?
butyrate + acetyl-CoA
acetate + butyryl-CoA
-
28% activity compared to propionate
-
-
?
butyryl-CoA + propanoate
?
-
2% activity compared to 3-hydroxybutyryl-CoA
-
-
?
crotonate + acetyl-CoA
acetate + crotonyl-CoA
-
28% activity compared to propionate
-
-
?
crotonyl-CoA + propanoate
?
-
2% activity compared to 3-hydroxybutyryl-CoA
-
-
?
isobutyryl-CoA + propanoate
?
-
6% activity compared to 3-hydroxybutyryl-CoA
-
-
?
lactate + acetyl-CoA
acetate + lactoyl-CoA
-
36% activity compared to propionate
-
-
?
propionate + acetyl-CoA
acetate + propionyl-CoA
-
propionate is the best substrate, 100% activity
-
-
?
propionyl-CoA + propanoate
?
-
27% activity compared to 3-hydroxybutyryl-CoA
-
-
?
succinyl-CoA + propanoate
?
-
1% activity compared to 3-hydroxybutyryl-CoA
-
-
?
valeryl-CoA + propanoate
?
-
3% activity compared to 3-hydroxybutyryl-CoA
-
-
?
3-hydroxybutyrate + acetyl-CoA
acetate + 3-hydroxybutanoyl-CoA
-
75% activity compared to propionate
-
-
?
3-hydroxybutyrate + acetyl-CoA
acetate + 3-hydroxybutanoyl-CoA
Cupriavidus necator H16 / ATCC 23440 / NCIB 10442 / S-10-1
-
75% activity compared to propionate
-
-
?
3-hydroxypropanoate + acetyl-CoA
acetate + 3-hydroxypropanoyl-CoA
-
80% activity compared to propionate
-
-
?
3-hydroxypropanoate + acetyl-CoA
acetate + 3-hydroxypropanoyl-CoA
Cupriavidus necator H16 / ATCC 23440 / NCIB 10442 / S-10-1
-
80% activity compared to propionate
-
-
?
4-hydroxybutyrate + acetyl-CoA
acetate + 4-hydroxybutanoyl-CoA
-
19% activity compared to propionate
-
-
?
4-hydroxybutyrate + acetyl-CoA
acetate + 4-hydroxybutanoyl-CoA
Cupriavidus necator H16 / ATCC 23440 / NCIB 10442 / S-10-1
-
19% activity compared to propionate
-
-
?
acetate + propanoyl-CoA
acetyl-CoA + propanoate
Cupriavidus necator H16 / ATCC 23440 / NCIB 10442 / S-10-1
-
-
-
-
?
acetyl-CoA + 2-hydroxybutyrate
acetate + 2-hydroxybutyryl-CoA
-
-
-
-
?
acetyl-CoA + 2-hydroxybutyrate
acetate + 2-hydroxybutyryl-CoA
-
-
-
-
?
acetyl-CoA + 3-hydroxybutyrate
acetate + 3-hydroxybutyryl-CoA
-
-
-
-
?
acetyl-CoA + 3-hydroxybutyrate
acetate + 3-hydroxybutyryl-CoA
-
-
-
-
?
acetyl-CoA + 3-hydroxybutyrate
acetate + 3-hydroxybutyryl-CoA
Cupriavidus necator H16 / ATCC 23440 / NCIB 10442 / S-10-1
-
-
-
-
?
acetyl-CoA + 3-hydroxypropionate
acetate + 3-hydroxypropionyl-CoA
-
-
-
-
?
acetyl-CoA + 3-hydroxypropionate
acetate + 3-hydroxypropionyl-CoA
-
-
-
-
?
acetyl-CoA + 3-mercaptopropionate
acetate + 3-mercaptopropionyl-CoA
-
-
-
-
?
acetyl-CoA + 3-mercaptopropionate
acetate + 3-mercaptopropionyl-CoA
-
-
-
-
?
acetyl-CoA + acetoacetate
acetate + acetoacetyl-CoA
Cupriavidus necator H16 / ATCC 23440 / NCIB 10442 / S-10-1
-
-
-
-
?
acetyl-CoA + acrylate
acetate + acryloyl-CoA
Cupriavidus necator H16 / ATCC 23440 / NCIB 10442 / S-10-1
-
-
-
-
?
acetyl-CoA + propanoate
acetate + propanoyl-CoA
-
best substrate
-
r
acetyl-CoA + propanoate
acetate + propanoyl-CoA
-
specific for monocarboxylic acids
-
r
acetyl-CoA + propanoate
acetate + propanoyl-CoA
-
reaction of (S)-alanine fermentation pathway
-
-
-
acetyl-CoA + propanoate
acetate + propanoyl-CoA
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
Cupriavidus necator H16 / ATCC 23440 / NCIB 10442 / S-10-1
-
100% activity
-
-
?
propionyl-CoA + succinate
propanoate + succinoyl-CoA
-
-
-
-
?
propionyl-CoA + succinate
propanoate + succinoyl-CoA
Propionibacterium freudenreichii DSM 4902
-
-
-
-
?
succinate + acetyl-CoA
acetate + succinyl-CoA
-
48% activity compared to propionate
-
-
?
succinate + acetyl-CoA
acetate + succinyl-CoA
Cupriavidus necator H16 / ATCC 23440 / NCIB 10442 / S-10-1
-
48% activity compared to propionate
-
-
?
additional information
?
-
-
The wild-type Pct is not able to efficiently convert lactate to lactyl-CoA
-
-
-
additional information
?
-
-
no activity with acetyl-CoA and formiate, acetoacetate, bromopropionate, glycine, pyruvate, 2-hydroxybutyrate, malonate, fumarate, itaconate, beta-alanine, gamma-aminobutyrate, levulate, glutarate or adipate as potential CoA acceptor. No activity with isovaleryl-CoA as CoA donor
-
-
-
additional information
?
-
Cupriavidus necator H16 / ATCC 23440 / NCIB 10442 / S-10-1
-
no activity with acetyl-CoA and formiate, acetoacetate, bromopropionate, glycine, pyruvate, 2-hydroxybutyrate, malonate, fumarate, itaconate, beta-alanine, gamma-aminobutyrate, levulate, glutarate or adipate as potential CoA acceptor. No activity with isovaleryl-CoA as CoA donor
-
-
-
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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
additional information
?
-
-
The wild-type Pct is not able to efficiently convert lactate to lactyl-CoA
-
-
-
acetate + propanoyl-CoA
acetyl-CoA + propanoate
Cupriavidus necator H16 / ATCC 23440 / NCIB 10442 / S-10-1
-
-
-
-
?
acetyl-CoA + propanoate
acetate + propanoyl-CoA
-
reaction of (S)-alanine fermentation pathway
-
-
-
acetyl-CoA + propanoate
acetate + propanoyl-CoA
Q9L3F7
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
Cupriavidus necator H16 / ATCC 23440 / NCIB 10442 / S-10-1
-
100% activity
-
-
?
propionyl-CoA + succinate
propanoate + succinoyl-CoA
-
-
-
-
?
propionyl-CoA + succinate
propanoate + succinoyl-CoA
Propionibacterium freudenreichii DSM 4902
-
-
-
-
?
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COFACTOR
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
IMAGE
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INHIBITOR
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
IMAGE
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ACTIVATING COMPOUND
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
IMAGE
propionate
increase in propionate concentration lead to increase of enzyme amount
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KM VALUE [mM]
SUBSTRATE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
IMAGE
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TURNOVER NUMBER [1/s]
SUBSTRATE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
IMAGE
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SPECIFIC ACTIVITY [µmol/min/mg]
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
additional information
-
development of propionate-detection systems, overview
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pH OPTIMUM
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
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pH RANGE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
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TEMPERATURE OPTIMUM
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
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TEMPERATURE RANGE
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
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ORGANISM
COMMENTARY
LITERATURE
UNIPROT
SEQUENCE DB
SOURCE
Propionibacterium freudenreichii subsp. shermanii
-
-
brenda
Propionibacterium freudenreichii DSM 4902
Propionibacterium freudenreichii subsp. shermanii
-
-
brenda
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UNIPROT
ENTRY NAME
ORGANISM
NO. OF AA
NO. OF TRANSM. HELICES
MOLECULAR WEIGHT[Da]
SOURCE
Sequence
I7FP88_MYCS2
Mycobacterium smegmatis (strain ATCC 700084 / mc(2)155)
529
0
56605
TrEMBL
A0A1N6CFV1_9MYCO
185
0
20721
TrEMBL
A0A0P0RHJ4_9BURK
673
0
73152
TrEMBL
Q2RJ16_MOOTA
Moorella thermoacetica (strain ATCC 39073 / JCM 9320)
527
0
57573
TrEMBL
A4SYB7_POLAQ
Polynucleobacter asymbioticus (strain DSM 18221 / CIP 109841 / QLW-P1DMWA-1)
666
0
72576
TrEMBL
A0A380F312_STACA
518
0
57775
TrEMBL
I4D6W6_DESAJ
Desulfosporosinus acidiphilus (strain DSM 22704 / JCM 16185 / SJ4)
524
0
56940
TrEMBL
A0A1M9GS61_9MYCO
528
0
57077
TrEMBL
Q7P7V6_FUSNV
406
0
44711
TrEMBL
Q9Y916_AERPE
Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1)
554
0
61889
TrEMBL
F7ZLI1_ROSLO
Roseobacter litoralis (strain ATCC 49566 / DSM 6996 / JCM 21268 / NBRC 15278 / OCh 149)
648
0
69733
TrEMBL
Q220N6_RHOFT
Rhodoferax ferrireducens (strain ATCC BAA-621 / DSM 15236 / T118)
650
0
69914
TrEMBL
Q8RFA2_FUSNN
Fusobacterium nucleatum subsp. nucleatum (strain ATCC 25586 / CIP 101130 / JCM 8532 / LMG 13131)
528
0
58233
TrEMBL
A0AKS6_LISW6
Listeria welshimeri serovar 6b (strain ATCC 35897 / DSM 20650 / SLCC5334)
527
0
56819
TrEMBL
A0A0H2YQC0_CLOP1
Clostridium perfringens (strain ATCC 13124 / DSM 756 / JCM 1290 / NCIMB 6125 / NCTC 8237 / Type A)
516
0
56049
TrEMBL
B1RAT1_CLOPF
516
0
56049
TrEMBL
A4WJA5_PYRAR
Pyrobaculum arsenaticum (strain DSM 13514 / JCM 11321)
543
0
59672
TrEMBL
E3HAR0_ILYPC
Ilyobacter polytropus (strain DSM 2926 / CuHBu1)
524
0
56818
TrEMBL
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MOLECULAR WEIGHT
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
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SUBUNIT
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
homotetramer
?
-
x * 55700, calculated from amino acid sequence; x * 56000, SDS-PAGE
?
Propionibacterium freudenreichii DSM 4902
-
x * 55700, calculated from amino acid sequence; x * 56000, SDS-PAGE
-
homotetramer
-
4 * 57000, calculated from amino acid sequence; 4 * 64000, SDS-PAGE
homotetramer
Cupriavidus necator H16 / ATCC 23440 / NCIB 10442 / S-10-1
-
4 * 57000, calculated from amino acid sequence; 4 * 64000, SDS-PAGE
-
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PROTEIN VARIANTS
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
V193A
-
the Pct540 mutant contains the V193A mutation, and four silent nucleotide exchanges of T78C, T669C, A1125G, T1158C
E342Q
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
E342Q
Cupriavidus necator H16 / ATCC 23440 / NCIB 10442 / S-10-1
-
the mutant shows 10% of wild type activity
-
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STORAGE STABILITY
ORGANISM
UNIPROT
LITERATURE
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PURIFICATION/commentary
ORGANISM
UNIPROT
LITERATURE
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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 BL21(DE3) cells
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APPLICATION
ORGANISM
UNIPROT
COMMENTARY
LITERATURE
biotechnology
synthesis
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
biotechnology
propionate-biosensor, using propionate coenzyme A transferase from Clostridium propionicum and short-chain acyl-CoA oxidase from Arabidopsis thaliana as enzyme electrodes
synthesis
-
engineered mutant Pct, coexpressed with an engineered Pseudomonas sp. MBEL 6-19 polyhydroxyalkanoate synthase 1, is able to produce poly(3-hydroxybutyrate-co-lactate) copolymers having 9-64 mol% of lactate. Polylactic acid might be a good alternative to petroleum-based plastic as it possesses several desirable properties such as biodegradability, biocompatibility, compostability, and low toxicity to humans
synthesis
-
in an engineered Escherichia coli strain JLX7, the engineered enzyme mutant Pct540, coexpressed with an engineered Pseudomonas sp. MBEL 6-19 polyhydroxyalkanoate synthase 1, is able to effectively produce polylactic acid, a promising biomass-derived polymer, overview
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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
brenda
Stadtman, E.R.
Acyl-coenzyme A synthesis by phosphotransacetylase and coenzyme A-transphorase
Fed. Proc.
11
291
1952
Clostridium kluyveri
-
brenda
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
brenda
Brock, M.; Buckel, W.
On the mechanism of action of the antifungal agent propionate
Eur. J. Biochem.
271
3227-3241
2004
Aspergillus nidulans
brenda
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
brenda
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)
brenda
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
brenda
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
brenda
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
brenda
Lindenkamp, N.; Schuermann, M.; Steinbuechel, A.
A propionate CoA-transferase of Ralstonia eutropha H16 with broad substrate specificity catalyzing the CoA thioester formation of various carboxylic acids
Appl. Microbiol. Biotechnol.
97
7699-7709
2012
Cupriavidus necator, Cupriavidus necator H16 / ATCC 23440 / NCIB 10442 / S-10-1
brenda
Yang, Y.H.; Brigham, C.J.; Song, E.; Jeon, J.M.; Rha, C.K.; Sinskey, A.J.
Biosynthesis of poly(3-hydroxybutyrate-co-3-hydroxyvalerate) containing a predominant amount of 3-hydroxyvalerate by engineered Escherichia coli expressing propionate-CoA transferase
J. Appl. Microbiol.
113
815-823
2012
Cupriavidus necator
brenda
Li, Y.F.; Wei, S.; Yu, Z.
Feedstocks affect the diversity and distribution of propionate coa-transferase genes (pct) in anaerobic digesters
Microb. Ecol.
66
351-362
2013
uncultured bacterium
brenda
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
brenda
Volodina, E.; Schuermann, M.; Lindenkamp, N.; Steinbuechel, A.
Characterization of propionate CoA-transferase from Ralstonia eutropha H16
Appl. Microbiol. Biotechnol.
98
3579-3589
2014
Cupriavidus necator, Cupriavidus necator H16 / ATCC 23440 / NCIB 10442 / S-10-1
brenda
Wang, Z.; Ammar, E.M.; Zhang, A.; Wang, L.; Lin, M.; Yang, S.T.
Engineering Propionibacterium freudenreichii subsp. shermanii for enhanced propionic acid fermentation: effects of overexpressing propionyl-CoA:succinate CoA transferase
Metab. Eng.
27
46-56
2015
Propionibacterium freudenreichii, Propionibacterium freudenreichii DSM 4902
brenda
Luo, H.; Zhou, D.; Liu, X.; Nie, Z.; Quiroga-Sanchez, D.L.; Chang, Y.
Production of 3-hydroxypropionic acid via the propionyl-CoA pathway using recombinant Escherichia coli strains
PLoS ONE
11
e0156286
2016
Megasphaera elsdenii
brenda
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