ZHANG Zhaohui, ZHANG Likun, LU Yuele. Production of R-metalaxyl by resolution of racemic metalaxyl using biocatalyst[J]. CIESC Journal, 2017, (11): 4229-4238.
ZHANG Zhaohui, ZHANG Likun, LU Yuele. Production of R-metalaxyl by resolution of racemic metalaxyl using biocatalyst[J]. CIESC Journal, 2017, (11): 4229-4238.DOI: 10.11949/j.issn.0438-1157.20170398.
A Gram-negative bacterium was isolated from the soil and sludge samples
which had high activity for enantioselective hydrolysis of (R
S)-metalaxyl. The strain was identified as Albibacters by 16S rDNA sequence analysis. It was named Albibacters sp. zjut528. At 37℃
15 g·L-1 of the wet cells (81% water content) catalyzed the hydrolysis of (R
S)-metalaxyl at the concentration of 50 g·L-1 for 28h
the yield reached 47.1% and the main product was R-metalaxyl acid with eep > 99.9%. In order to isolate its intracellular esterase
the cells were disrupted by ultrasonic. After centrifugation
the supernatant was treated by ammonium sulfate precipitation
followed by ion-exchange chromatography and gel filtration chromatography. A SDS-PAGE electrophoresis-pure esterase protein was obtained with a molecular mass of about 40×103. Its N-terminal amino acid sequence was determined as NH2-Ala-Ala -Lys-Ala-Pro-Leu-Arg-Leu-Lys-Glu. Its optimum catalytic temperature and pH were 40℃ and 9.0
respectively. The enzyme was stable at 20-40℃ and pH 5.0-10.0. 0.2 mmol·L-1 of Fe2+
Mn2+
Zn2+ can improve its activity
but Fe3+ inhibited it. Its activity was highly improved when some organic solvents
such as acetonitrile
isopropanol
acetone
isopropyl ether
cyclohexane and n-hexane
were added at the concentration of 20% (vol). The Michaelis-Menten kinetics parameters for the enzyme were Vm=0.18 mmol·L-1·min-1
Km=2.29 mmol·L-1 and Kcat=0.85 min-1. A new process for producing R-matalaxyl from R
S-matalaxyl was established by using Albibacters sp. zjut528 cells as the catalyst. First
the cells catalyzed enantioeletive hydrolysis of (R
S)-matalaxyl to produce R-metalaxyl. After reaction
the R-metalaxyl acid and the unreacted S-matalaxyl were separated by extraction. R-Metalaxy acid was esterified with methanol to produce R-metalaxyl. Followed by some separation steps
the final product of R-metalaxy was obtained. Its purity was 96.2% and ee value was 99.3%. The unreacted S-metalaxyl can be reused by racemization. After heated for 6 h at 60℃