Transcription regulatory factor and its mutant and its application in the preparation of vitamin b12
A technology for transcriptional regulators, vitamins, applied in applications, microorganism-based methods, microorganisms, etc., can solve problems such as affecting vitamin B production
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preparation example Construction
[0035] (2) Preparation of standard products
[0036] Configuration gradient vitamin B 12Standards (20 mg / L, 50 mg / L, 100 mg / L, 150 mg / L).
[0037] (3) HPLC detection conditions
[0038] C18-250A column (Agilent, 4.6 mmid 9 × 250 mm, 5 µm). The mobile phase was 70% organic phase (acetonitrile) and 30% inorganic phase (sodium acetate aqueous solution), the absorption wavelength was 361 nm, the column temperature was 35 °C, the flow rate was 0.8 mL / min, and the injection volume was 20 µL.
[0039] (4) Vitamin B 12 Drawing of standard curve
[0040] Standards with different concentrations were detected by HPLC according to the above conditions, and the peak areas A-VB were drawn 12 Concentration standard curve. Taking the measured peak area A as the ordinate, vitamin B 12 The mass concentration C (mg / L) is recorded as the abscissa, and vitamin B is drawn 12 standard curve line. See Image 6 , get the regression equation y=19.846x-80.857, R 2 =0.999, the absorbance has a...
Embodiment 1
[0041] Example 1: Determination of mutagenesis time by atmospheric room temperature plasma (ARTP), construction of mutant library and acquisition of high-yielding strains
[0042] (1) Determination of lethality
[0043] In order to obtain a relatively broad mutant library, we carried out atmospheric room temperature plasma (ARTP) mutagenesis on the chassis cell Sinorhizobium meliloti CGMCC NO.9638. First, the lethality of CGMCCNO.9638 was determined under plasma mutagenesis conditions. CGMCC NO.9638 cells (OD 600 =1) Rinse twice with 0.85% NaCl solution, then dilute to 10 with 0.85% NaCl solution 8 cells / mL suspension. Take 10uL of the suspension and spread it evenly on the iron sheet, and carry out ARTP mutagenesis. Three replicates were plated for each time point. After mutagenesis, place the iron sheet with cells in 1 mL of sterile water and vortex to wash the cells, and dilute the cell suspension 10 times to 10 -3 , Take 100 μL of the diluted cell suspension and spre...
Embodiment 2
[0053] Example 2: Comparative genome analysis of mutant strains and starting strains
[0054] The strain SM* and the starting strain CGMCC NO.9638 were sent to Jinweizhi Biotechnology Co., Ltd. for whole genome sequencing. By comparing the whole genome sequences of the two strains, it was found that 5 transcriptional regulators had point mutations, as shown in Table 2. In order to verify the effect of the mutation site on vitamin B 12 For the impact on yield, we overexpressed the mutated transcriptional regulator gene in the starting strain CGMCC NO.9638.
[0055]
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