Recombinant escherichia coli and application thereof to 2-butanol production
A technology for recombining Escherichia coli and Escherichia coli, which is applied in the direction of microorganism-based methods, bacteria, microorganisms, etc., can solve the problems of high cost, low product productivity, and difficulty in large-scale production, and achieve low cost, convenient operation, and low cost. Effect
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Embodiment 1
[0041] Example 1: Construction of Escherichia coli co-expressing formate dehydrogenase gene fdh and alcohol dehydrogenase gene adh
[0042] (1) Cloning of gene fdh: Genomic DNA of bacterial strain Candida boidinii (Candidaboidinii) NCYC1513 is prepared by a conventional method, and this process can refer to a small amount of genome in "Guide to Molecular Biology" published by Science Press. The preparation method is to extract the genomic DNA of CandidaboidiniiNCYC1513; use synthetic primers to amplify the formate dehydrogenase gene fdh from the genomic DNA of CandidaboidiniiNCYC1513 by PCR;
[0043] CandidaboidiniiNCYC1513 is used as the source bacterium of the fdh gene. According to the genome sequence of the bacterium that has been sequenced, primers are designed to introduce NdeI and XhoI restriction enzyme sites that can be inserted into the plasmid pETDute-1 (Novagen). The primer sequences are as follows:
[0044] Upstream primer 5'- CATATG AAGATCGTTTTAGTCTTATATGATGCTG...
Embodiment 2
[0052] Example 2: Preparation of Whole Cell Catalyst
[0053] (1) Plate culture: Streak Escherichia coli (Escherichiacoli) BL21 / pETDuet-fdh-adh on an LB plate containing 1.5 to 1.8% agar in mass volume ratio and 100 μg / mL ampicillin, and culture at 37±1°C for 12 ±1 hour;
[0054] (2) First-class seeds: under sterile conditions, pick a single colony on the flat plate of step (1) with a sterile toothpick, and then inoculate it into 5 mL of LB liquid medium containing 100 μg / mL ampicillin, Shaking culture at 37±1°C for 12±1 hours;
[0055] (3) Secondary seeds: under aseptic conditions, take the bacterial solution cultivated in step (2) and inoculate 100 mL of LB liquid culture medium containing 100 μg / mL of ampicillin with a volume ratio of 1 to 2%. medium, 37±1°C shaker culture for 12±1 hours;
[0056] (4) Shake flask culture: under aseptic conditions, take the bacterial solution obtained in step (3) and inoculate it into 1 L of LB liquid medium with an inoculum volume ratio ...
Embodiment 3
[0059] Embodiment 3: utilize the biocatalyst that embodiment 2 obtains to prepare 2-butanol
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