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

BRENDA support

Literature summary for 1.1.1.B18 extracted from

  • Yamamura, E.T.
    Construction of Rhodococcus expression vectors and expression of the aminoalcohol dehydrogenase gene in Rhodococcus erythropolis (2018), Biosci. Biotechnol. Biochem., 82, 1396-1403 .
    View publication on PubMed

Application

Application Comment Organism
pharmacology the enzyme produces double chiral aminoalcohols, which are used as pharmaceuticals. The Rhodococcus expression vector, pRET11100, constructed by removing aadh from the pRET1172 plasmid may be useful for bioconversion Rhodococcus erythropolis

Cloned(Commentary)

Cloned (Comment) Organism
construction of Rhodococcus expression vectors, derived from the Rhodococcus/Escherichia coli shuttle vector pRET1102, to express aadh. The plasmid pRET1102 can be transformed into many actinomycete strains, including Rhodococcus erythropolis. The transformation efficiency for a species closely related to Rhodococcus erythropolis is higher than that for other actinomycete strains. Promoters of various strengths, hsp, 1200rep, and TRR, are obtained from Gram-positive bacteria. The activity of TRR is stronger than that of hsp and 1200rep. The aadh-expressing plasmid pRET1172 with TRR can be transformed into many actinomycete strains to increase their AADH production. The Rhodococcus expression vector, pRET11100, constructed by removing aadh from the pRET1172 plasmid may be useful for bioconversion Rhodococcus erythropolis

Organism

Organism UniProt Comment Textmining
Rhodococcus erythropolis A1IG83
-
-
Rhodococcus erythropolis MAK154 A1IG83
-
-

Synonyms

Synonyms Comment Organism
AADH
-
Rhodococcus erythropolis
NADP+-dependent aminoalcohol dehydrogenase
-
Rhodococcus erythropolis