A dna fragment with promoter function and its application
A technology of promoters and fragments, applied in the field of DNA fragments, can solve the problems of difficult search, low start-up efficiency, unsustainable expression, etc., and achieve the effect of high activity
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[0035] (1) Bacterial cultivation: Take out the Bacillus licheniformis ATCC14580 (-80°C) glycerol tube and streak it on an LB solid plate for 16 hours at 37°C, pick a single colony in 10 mL of LB liquid medium containing 1% final concentration of starch , 37°C, 200rpm to OD 600 20-25 (spectrophotometer, Hitachi, Japan).
[0036] (2) Extraction of bacterial total RNA and RNA-Seq sequencing: 1 mL of cell culture solution obtained in step (1) was collected and centrifuged at 8000 g for 1 min to extract total bacterial RNA (see figure 1 ). For the specific extraction method, refer to the Cellular Bacterial Total RNA Extraction Kit from Omega Bio-tek Company. The samples used for RNA-Seq sequencing library preparation were qualified by the Agilent Technologies 2100 Bioanalyzer, and the mixed DNA molecules were treated with DNaseI (RNase Free), and Ribo-Zero (Gram-Positive Bacteria) kit (USA) was used to remove most of the total RNA rRNA, purified mRNA. The mRNA was first broken...
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