TY - JOUR
T1 - Rhodococcus strains as source for ene-reductase activity
AU - Chen, Bi Shuang
AU - Médici, Rosario
AU - van der Helm, Michelle P.
AU - van Zwet, Ymke
AU - Gjonaj, Lorina
AU - van der Geest, Roelien
AU - Otten, Linda G.
AU - Hanefeld, Ulf
PY - 2018
Y1 - 2018
N2 - Rhodococcus strains are ubiquitous in nature and known to metabolise a wide variety of compounds. At the same time, asymmetric reduction of C=C bonds is important in the production of high-valued chiral building blocks. In order to evaluate if Rhodococci can be used for this task, we have probed several Rhodococcus rhodochrous and R. erythropolis strains for ene-reductase activity. A series of substrates including activated ketones, an aldehyde, an imide and nitro-compound were screened using whole cells of seven Rhodococcus strains. This revealed that whole cells of all Rhodococcus strains showed apparent (S)-selectivity towards ketoisophorone, while most other organisms show (R)-selectivity for this compound. Three putative ene-reductases from R. rhodochrous ATCC 17895 were heterologously expressed in Escherichia coli. One protein was purified and its biocatalytic and biochemical properties were characterised, showing typical (enantioselective) properties for class 3 ene-reductases of the old yellow enzyme family.
AB - Rhodococcus strains are ubiquitous in nature and known to metabolise a wide variety of compounds. At the same time, asymmetric reduction of C=C bonds is important in the production of high-valued chiral building blocks. In order to evaluate if Rhodococci can be used for this task, we have probed several Rhodococcus rhodochrous and R. erythropolis strains for ene-reductase activity. A series of substrates including activated ketones, an aldehyde, an imide and nitro-compound were screened using whole cells of seven Rhodococcus strains. This revealed that whole cells of all Rhodococcus strains showed apparent (S)-selectivity towards ketoisophorone, while most other organisms show (R)-selectivity for this compound. Three putative ene-reductases from R. rhodochrous ATCC 17895 were heterologously expressed in Escherichia coli. One protein was purified and its biocatalytic and biochemical properties were characterised, showing typical (enantioselective) properties for class 3 ene-reductases of the old yellow enzyme family.
KW - Asymmetric reduction
KW - Enantioselectivity
KW - Ene-reductase
KW - Rhodococcus
UR - http://resolver.tudelft.nl/uuid:b7b0f93f-4b18-4bf5-82ec-fa7ea0c38d67
UR - http://www.scopus.com/inward/record.url?scp=85046023762&partnerID=8YFLogxK
U2 - 10.1007/s00253-018-8984-7
DO - 10.1007/s00253-018-8984-7
M3 - Article
AN - SCOPUS:85046023762
SP - 1
EP - 12
JO - Applied Microbiology and Biotechnology
JF - Applied Microbiology and Biotechnology
SN - 0175-7598
ER -