Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary extracted from

  • Ji, J.; Fan, K.; Tian, X.; Zhang, X.; Zhang, Y.; Yang, K.
    Iterative combinatorial mutagenesis as an effective strategy for generation of deacetoxycephalosporin C synthase with improved activity toward penicillin G (2012), Appl. Environ. Microbiol., 78, 7809-7812.
    View publication on PubMedView publication on EuropePMC

Protein Variants

EC Number Protein Variants Comment Organism
1.14.20.1 C155Y site-directed mutagenesis Streptomyces clavuligerus
1.14.20.1 C155Y/Y184H/V275I/C281Y site-directed mutagenesis, the mutant shows increased activity with penicillin G compared to the wild-type enzyme Streptomyces clavuligerus
1.14.20.1 C281Y site-directed mutagenesis Streptomyces clavuligerus
1.14.20.1 I305L site-directed mutagenesis, the mutant shows increased activity with penicillin G compared to the wild-type enzyme Streptomyces clavuligerus
1.14.20.1 I305M site-directed mutagenesis, the mutant shows increased activity with penicillin G compared to the wild-type enzyme Streptomyces clavuligerus
1.14.20.1 I305M/S261M site-directed mutagenesis, the mutant shows increased activity with penicillin G compared to the wild-type enzyme Streptomyces clavuligerus
1.14.20.1 I305M/T213V site-directed mutagenesis, the mutant shows increased activity with penicillin G compared to the wild-type enzyme Streptomyces clavuligerus
1.14.20.1 I305M/T213V/M73T site-directed mutagenesis, the mutant shows increased activity with penicillin G compared to the wild-type enzyme Streptomyces clavuligerus
1.14.20.1 I305M/T213V/S261M site-directed mutagenesis, the mutant shows increased activity with penicillin G compared to the wild-type enzyme Streptomyces clavuligerus
1.14.20.1 M73T site-directed mutagenesis Streptomyces clavuligerus
1.14.20.1 additional information since the natural substrate of the enzyme, penicillin N, is not available in large quantities, engineering of a scDAOCS capable of converting the cheap and easily available substrate penicillin G is valuable for large-scale production of 7-aminodeacetoxycephalosporanic acid, 7-ADCA Streptomyces clavuligerus
1.14.20.1 N304K site-directed mutagenesis Streptomyces clavuligerus
1.14.20.1 Q126M site-directed mutagenesis Streptomyces clavuligerus
1.14.20.1 S261A site-directed mutagenesis Streptomyces clavuligerus
1.14.20.1 S261M site-directed mutagenesis Streptomyces clavuligerus
1.14.20.1 T213V site-directed mutagenesis Streptomyces clavuligerus
1.14.20.1 V275I site-directed mutagenesis Streptomyces clavuligerus
1.14.20.1 Y184H site-directed mutagenesis Streptomyces clavuligerus

KM Value [mM]

EC Number KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
1.14.20.1 1.6
-
penicillin G mutant C155Y/Y184H/V275I/C281Y, pH and temperature not specified in the publication Streptomyces clavuligerus
1.14.20.1 1.62
-
penicillin G mutant I305M/S261M, pH and temperature not specified in the publication Streptomyces clavuligerus
1.14.20.1 1.92
-
penicillin G mutantI305M/T213V/M73T, pH and temperature not specified in the publication Streptomyces clavuligerus
1.14.20.1 2.1
-
penicillin G mutant I305L, pH and temperature not specified in the publication Streptomyces clavuligerus
1.14.20.1 2.49
-
penicillin G mutant I305M/T213V/S261M, pH and temperature not specified in the publication Streptomyces clavuligerus
1.14.20.1 3.22
-
penicillin G mutant I305M/T213V, pH and temperature not specified in the publication Streptomyces clavuligerus
1.14.20.1 3.58
-
penicillin G mutant I305M, pH and temperature not specified in the publication Streptomyces clavuligerus
1.14.20.1 14.38
-
penicillin G wild-type enzyme, pH and temperature not specified in the publication Streptomyces clavuligerus

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
1.14.20.1 penicillin N + 2-oxoglutarate + O2 Streptomyces clavuligerus the enzyme catalyzes the ring expansion of penicillin substrates into a ring-expanded product to produce cephamycin C deacetoxycephalosporin C + succinate + CO2 + H2O
-
?

Organism

EC Number Organism UniProt Comment Textmining
1.14.20.1 Streptomyces clavuligerus
-
-
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.14.20.1 penicillin G + 2-oxoglutarate + O2
-
Streptomyces clavuligerus phenylacetyl-7-aminodeacetoxycephalosporanic acid + succinate + CO2 + H2O
-
?
1.14.20.1 penicillin N + 2-oxoglutarate + O2
-
Streptomyces clavuligerus deacetoxycephalosporin C + succinate + CO2 + H2O
-
?
1.14.20.1 penicillin N + 2-oxoglutarate + O2 the enzyme catalyzes the ring expansion of penicillin substrates into a ring-expanded product to produce cephamycin C Streptomyces clavuligerus deacetoxycephalosporin C + succinate + CO2 + H2O
-
?

Synonyms

EC Number Synonyms Comment Organism
1.14.20.1 DAOCS
-
Streptomyces clavuligerus

Turnover Number [1/s]

EC Number Turnover Number Minimum [1/s] Turnover Number Maximum [1/s] Substrate Comment Organism Structure
1.14.20.1 0.054
-
penicillin G wild-type enzyme, pH and temperature not specified in the publication Streptomyces clavuligerus
1.14.20.1 0.23
-
penicillin G mutant C155Y/Y184H/V275I/C281Y, pH and temperature not specified in the publication Streptomyces clavuligerus
1.14.20.1 0.37
-
penicillin G mutant I305L, pH and temperature not specified in the publication Streptomyces clavuligerus
1.14.20.1 0.537
-
penicillin G mutant I305M/S261M, pH and temperature not specified in the publication Streptomyces clavuligerus
1.14.20.1 0.589
-
penicillin G mutantI305M/T213V/M73T, pH and temperature not specified in the publication Streptomyces clavuligerus
1.14.20.1 0.65
-
penicillin G mutant I305M, pH and temperature not specified in the publication Streptomyces clavuligerus
1.14.20.1 0.654
-
penicillin G mutant I305M/T213V, pH and temperature not specified in the publication Streptomyces clavuligerus
1.14.20.1 0.668
-
penicillin G mutant I305M/T213V/S261M, pH and temperature not specified in the publication Streptomyces clavuligerus

kcat/KM [mM/s]

EC Number kcat/KM Value [1/mMs-1] kcat/KM Value Maximum [1/mMs-1] Substrate Comment Organism Structure
1.14.20.1 0.004
-
penicillin G wild-type enzyme, pH and temperature not specified in the publication Streptomyces clavuligerus
1.14.20.1 0.144
-
penicillin G mutant C155Y/Y184H/V275I/C281Y, pH and temperature not specified in the publication Streptomyces clavuligerus
1.14.20.1 0.176
-
penicillin G mutant I305L, pH and temperature not specified in the publication Streptomyces clavuligerus
1.14.20.1 0.182
-
penicillin G mutant I305M, pH and temperature not specified in the publication Streptomyces clavuligerus
1.14.20.1 0.203
-
penicillin G mutant I305M/T213V, pH and temperature not specified in the publication Streptomyces clavuligerus
1.14.20.1 0.268
-
penicillin G mutant I305M/T213V/S261M, pH and temperature not specified in the publication Streptomyces clavuligerus
1.14.20.1 0.307
-
penicillin G mutantI305M/T213V/M73T, pH and temperature not specified in the publication Streptomyces clavuligerus
1.14.20.1 0.332
-
penicillin G mutant I305M/S261M, pH and temperature not specified in the publication Streptomyces clavuligerus