Method for producing 2R,3R-butanediol by utilizing Klebsiella pneumoniae
A technology based on Klebsiella pneumoniae and butanediol, applied in the direction of microorganism-based methods, biochemical equipment and methods, microorganisms, etc., to achieve the effect of improving overall economic benefits
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Embodiment 1
[0029] The CGMCC1.6366 strain in this example is preserved by the China General Microorganism Culture Collection and Management Center, and has ampicillin resistance.
[0030] 1) Prepare seed medium
[0031] Peptone 10g / L, yeast powder 5g / L, sodium chloride 5g / L, prepared with tap water, dispensed into 250mL Erlenmeyer flasks with a liquid volume of 50mL, and sterilized.
[0032] 2) Allocation of glycerol, nitrogen source, phosphorus source and other components to make fermentation medium
[0033] Glycerin 30g / L, Ammonium Sulfate 4g / L, Dipotassium Hydrogen Phosphate 0.69g / L, Potassium Dihydrogen Phosphate 0.25g / L, Magnesium Sulfate 0.2g / L, Yeast Powder 1.5g / L, Trace Elements 1.0ml / L, Iron solution 1.0ml / L.
[0034] Among them, trace elements are: manganese sulfate 100mg / L, zinc chloride 70mg / L, sodium molybdate 35mg / L, boric acid 60mg / L, cobalt chloride 200mg / L, copper sulfate 29.28mg / L, nickel chloride 25mg / L L, concentrated hydrochloric acid (37%) 0.9ml / L.
[0035] The i...
Embodiment 2
[0043] 1. Construction of Klebsiella pneumoniae CGMCC1.6366budC mutant strain
[0044] Proceed as follows:
[0045] 1. Use PCR to amplify Klebsiella pneumoniae butanediol dehydrogenase (budC) and the upstream and downstream adjacent sequences, connect to the cloning vector by TA cloning method, and perform DNA sequence determination.
[0046] According to the genome information of Klebsiella pneumoniae MGH78578 (Genbank: CP000647), the butanediol dehydrogenase PCR primers were designed, the upstream primer budC-s: GCCATCCAGGAAGAGAAAAAATATCA (shown in SEQ ID NO.1), the downstream primer budC-a: AGACGTTTGTACGCCTGGGTAGAAG (shown in SEQ ID NO.2).
[0047] Using the above primers, Klebsiella pneumoniae CGMCC1.6366 genomic DNA was used as a template to amplify by PCR to obtain butanediol dehydrogenase (budC) gene fragment, which was connected to the pMD-18T simple plasmid (commercial product), named as pMD18T-budC plasmid, the sequence results are as follows:
[0048] The sequenc...
Embodiment 3
[0083] 1) Prepare seed medium and fermentation medium
[0084] Prepare seed medium and fermentation medium according to Example 1.
[0085] 2) Seed culture
[0086] Insert the Klebsiella pneumoniae CGMCC1.6366-budC- bacterial lawn prepared in Example 2 into the Erlenmeyer flask equipped with the seed medium, aerobic culture in a shaker at 42°C, and the rotation speed is 200 rpm, and cultivate for 12 Hour.
[0087] 3) Fermentation culture
[0088] Put a bottle of cultivated seeds into a 5L fermenter with 4L fermentation medium, ventilation rate 1L per minute, stirring speed 150 rpm, temperature 42°C, use sodium hydroxide solution to control the fermentation process pH7.5 , when the glycerol concentration was reduced to 5g / L, feed glycerin, control the glycerol concentration in the range of 5-40g / L, and ferment and cultivate for 70 hours.
[0089] According to the gas chromatographic conditions in Example 1, the fermentation broth components were detected, and the results we...
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