Furfural-resistant zymomonas mobilis and preparation method and application thereof
A technology for Zymomonas and furanaldehyde, which is applied in the field of bioengineering, can solve problems such as improving the tolerance of furanaldehyde, and achieves the effects of less demanding process requirements, excellent tolerance, and increased yield
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Embodiment 1
[0030] Construction of recombinant plasmids
[0031] Using the GeneMorph Ⅱ Random Mutagenesis Kit to perform error-prone polymerase chain reaction on the PCR product of RpoD, the mutant RpoD gene with point mutations of K219E, V522G and Q649L was screened out. The reaction product was purified using the E.Z.N.A? Gel Extraction Kit, the concentration of the low-melting point agarose gel was 1%, and the Bam H I and Xba I treatment, and then ligated to the restriction site corresponding to the plasmid pBBR1MCS-tet to obtain the recombinant plasmid, said pBBR1MCS-tet contains the promoter and terminator of pyruvate decarboxylase.
[0032] Construction of control plasmid
[0033] After purifying the PCR product of RpoD using E.Z.N.A? Gel Extraction Kit, use Bam H I and Xba I treatment, and then ligated to the restriction site corresponding to the plasmid pBBR1MCS-tet to obtain the control plasmid, said pBBR1MCS-tet contains the promoter and terminator of pyruvate decarbox...
Embodiment 2
[0035] Preparation of furan formaldehyde-resistant Zymomonas mobilis (strain of the present invention):
[0036] The recombinant plasmid obtained in Example 1 was transformed into Z.mobilis ZM4 by means of electroporation, and the bacteria transformed by the plasmid were spread on the RM agar solid plate medium containing 5 μg / ml tetracycline, and single clones were scraped. Place in RM liquid medium and culture overnight at 30°C.
[0037]According to 10% (v / v), the overnight culture liquid was added to 10ml RM liquid medium with furan formaldehyde concentration of 1g / L, 2g / L and 3g / L for cultivation, and then the obtained culture was spread on furan Cultured on a solid medium with a formaldehyde concentration of 3% and 5 μg / ml tetracycline, picked a single clone, extracted the plasmid, and sequenced the DNA.
[0038] Preparation of control strains:
[0039] The control plasmid obtained in Example 1 was transformed into Z. mobilis ZM4 by means of electroporation, and the bac...
Embodiment 3
[0041] The furfuralaldehyde-resistant Zymomonas mobilis and the control strain of Example 2 were cultured on RM liquid medium at 30° C. until the OD600 was 1.0, and then 10-fold serial dilution was performed. Each dilution was placed in RM solid medium with different concentrations of furfuraldehyde, and cultured at 30° C. for 4-5 days.
[0042] When drawing the growth curves of the bacterial strains of the present invention and the control bacterial strains, the bacteria were placed in the Bioscreen C system for cultivation. At 10% (V / V) inoculum size, overnight bacteria were respectively placed in 1ml of fresh RM liquid medium with furfuraldehyde concentration of 2g / L and 3g / L for cultivation, and the initial OD600 value was 0.15-0.2. Then the bacteria were added to the sample wells of the Bioscreen plate, 300 μl per well, and three groups of parallel samples were set up. The temperature is controlled at 30 degrees Celsius, the detection optical density is 600nm, and the ab...
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