Lentinus edodes laccase lelac11 and its application in improving microbial stress tolerance
A technology of stress tolerance and laccase, applied in the field of oxidase, can solve the problems of decreased yield, decreased mycelial growth rate, decreased quality and the like of Lentinus edodes, and achieves the effects of improving stress tolerance and stress tolerance.
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Embodiment 1
[0049] Construction of Laccase LeLac11 Overexpression Vector pET30a / LeLac11 in Example 1 Lentinus edodes 18
[0050] First, design primers to amplify the target gene LeLac11 fragment from the original plasmid, and then recombine it into the digested overexpression vector pET30a through the seamless cloning recognition sites at both ends of the primer; transfer the ligated product into the prepared The competent cells of Escherichia coli BL21 were sent to Sangon Bioengineering (Shanghai) Co., Ltd. for sequencing and identification of the grown monoclonal colonies. The correct clone sequence was compared to the successfully constructed overexpression plasmid pET30a / LeLac11. After success, the graph is as follows Figure 5 shown.
[0051] 1. Design and synthesize primers
[0052] (1) Design PCR amplification fragment primers, and introduce homologous sequences at the ends of the linearized cloning vector at the 5' end of the primers, so that the 5' and 3' end sequences of the a...
Embodiment 2
[0088] Prokaryotic expression of embodiment 2 mushroom laccase LeLac11 gene
[0089] 1. Inoculate a single colony of Escherichia coli BL21 containing pET30a / LeLac11 in 100mL LB liquid medium containing 100μg / mL Kan, culture at 220rpm, 37℃ until the OD600 reaches 0.6-0.8, and then add IPTG with a concentration of 1mM to In 100mL liquid LB, continue to culture at 220rpm, 37°C for 4h, in order to achieve the purpose of optimizing the induction culture conditions. At the same time, the empty vector pET30a was transformed into BL21 as a control.
[0090]2. Extract prokaryotic expressed protein for SDS-PAGE electrophoresis
[0091] ①Protein sample preparation
[0092] (1) Take 1 mL of the bacterial solution from Step 1 and add it to 100 mL of LB liquid medium containing 100 μg / mL Kan, incubate at 37°C and 220 r / min for 2.5-3 hours, and use a UV spectrophotometer to detect when the OD 600 reaches 0.4-0.6 , adding IPTG with a concentration of 1 mM for induction;
[0093] (2) After...
Embodiment 3
[0107] Embodiment 3 Research on the cold-resistant function of Lentinus edodes laccase LeLac11
[0108] 1. Take 50 μL of the verified bacterial solution, inoculate it into 50 mL of LB (containing 100 μg / mL Kan) liquid medium, incubate at 37°C and 150 r / min for 2.5-3 hours, and use a UV spectrophotometer to detect when the OD600 reaches 0.4-0.6 , adding 1 mM IPTG for induction.
[0109] 2. Placed in an incubator at 4°C, and subjected to cold stress for 12h, 24h, 36h, 48h, 60h.
[0110] 3. Take 3 mL of the bacterial liquid after cold stress treatment, detect the absorbance at 600 nm with an ultraviolet spectrophotometer, and record the data. Three replicates were set for each experimental gradient.
[0111] 4. Take the absorbance of the OD600 of the bacterium solution at 0h as a control, calculate the growth rate of Escherichia coli containing pET30a / LeLac11 and Escherichia coli containing pET30a, and make a line graph of growth rate after cold stress (note: growth rate=cold-t...
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