Enterobacter cloacae zjph1903 and its application
A ZJPH1903, Enterobacter cloacae technology, applied in the direction of bacteria, microorganisms, biochemical equipment and methods, etc., can solve the problems of difficult operation control, high cost and limited industrial application, etc., achieve good stereoselectivity, improve catalytic efficiency, and product optics The effect of high purity
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Embodiment 1
[0033] Example 1, strain screening, biotransformation and analysis and detection of transformed products, strain identification
[0034] 1) Strain screening:
[0035] The source of the strain: Enterobacter cloacae (Enterobacter cloacae) ZJPH1903 was obtained by isolation and screening from soil samples collected near the pharmaceutical factory in Binjiang District, Hangzhou City, Zhejiang Province. The specific screening method is as follows: add 1g of soil sample to 100ml sterile In a 250ml Erlenmeyer flask of water, shake at 30°C and 200rpm for 0.5h to obtain a soil sample dilution. Take 1ml of the above diluted solution and add it to a 250ml Erlenmeyer flask containing 100ml enriched medium, culture at 30°C and 200rpm for 5 days, after the culture medium becomes turbid, take 1ml of the culture medium and add it to the fresh enriched medium , cultivated under the same conditions for several days, and repeated the enrichment culture for 3 to 4 times. 2,2',4'-Trichloroacetop...
Embodiment 2
[0054] Embodiment 2: the acquisition of wet thalline
[0055] 1) Slant culture: Pick a single colony of Enterobacter cloacae ZJPH1903 and inoculate it into the slant medium, culture at 30°C for 36 hours, and store in a refrigerator at 4°C for later use; the final concentration of the slant medium is composed of: glucose 15g / L, peptone 20g / L L, yeast extract 10g / L, (NH 4 ) 2 SO 4 2g / L, KH 2 PO 4 2g / L, NaCl 1g / L, MgSO 4 ·7H 2 O 0.5g / L, agar 20g / L, solvent is water, pH value 6.5.
[0056] 2) Seed culture: Pick a ring of bacteria from the mature slant and insert it into the seed medium, and cultivate it at 30°C and 200rpm for 12 hours to obtain the seed liquid; the formula of the seed medium: glucose 15g / L, peptone 20g / L, yeast Paste 10g / L, (NH 4 ) 2 SO 4 2g / L, KH 2 PO 4 2g / L, NaCl 1g / L, MgSO 4 ·7H 2 O 0.5g / L, the solvent is water, and the pH value is 6.5.
[0057] 3) Fermentation culture: Transfer the seed solution to the fermentation medium with an inoculation ...
Embodiment 3
[0059] The wet bacteria obtained in Example 2 were suspended in 10 mL of different reaction media (pH 7.0), and the concentration of the wet bacteria was 100 g / L reaction medium by wet weight; 2 g / L of 2,2',4'-tri Chloroacetophenone substrate, then add 100g / L glucose as an auxiliary substrate, and place it in a shaker at 30°C and 200rpm for 24h. After the reaction, the reaction solution was centrifuged, and the supernatant was taken, and the detection method of Example 1 was used to measure the yield and optical properties of the product (R)-2-chloro-1-(2,4-dichlorophenyl)ethanol. Purity, as can be seen from Table 1, when the buffer is a phosphate buffer, the yield of (R)-2-chloro-1-(2,4-dichlorophenyl)ethanol is the highest, with a yield of 55.3%, e.e. The value is greater than 99.9%.
[0060] The influence of table 1 different reaction medium on productive rate and e.e. value
[0061]
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