Enzyme for high yield of specific functional oligopeptides and derived from Aspergillus niger and engineering bacteria thereof
A technology of engineering bacteria and oligopeptides, applied in the field of genetic engineering, can solve the problems of high purification costs, cumbersome treatment procedures, and large limitations, and achieve the effects of reducing environmental pollution, reducing production costs, and improving efficiency
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Embodiment 1
[0022] Example 1 Construction of M00988 CPA mutant
[0023] 1. Cloning of Aspergillus niger M00988 CPA and construction of expression vector
[0024] According to the carboxypeptidase gene sequence from Aspergillus niger from NCBI, two pairs of primers CPA-F / CPA-R were designed, and the sequences are shown in Table 1.
[0025] Table 1 Sequences of carboxypeptidase gene cloning primers
[0026] The DNA of Aspergillus niger M00988 was extracted as a template, the sequence is shown in SEQ ID NO: 6, and the target gene fragment CPA was obtained by PCR amplification with CPA-F / CPA-R primers. PCR amplification conditions were: pre-denaturation at 94 °C for 5 min, then denaturation at 94 °C for 30 s, annealing at 68 °C for 1 min, extension at 72 °C for 1 min, 35 cycles, and extension at 72 °C for 10 min to obtain a fragment of about 1500 bp in size, which was detected by agarose electrophoresis like figure 1 shown.
[0027] Using the obtained target gene fragment CPA as a temp...
Embodiment 2
[0039] Example 2 Preparation and application of high F value oligopeptide
[0040] 1. Chlorella Protein Extraction
[0041] Accurately weigh a certain amount of Chlorella powder, add deionized water at a ratio of 1:48 (m / V) to the liquid, stir and shake at room temperature for 12 hours to swell. Add 5.37% solid sodium hydroxide to the chlorella suspension, pay attention to slow addition during the addition process, and keep stirring. After completion, sonicate for 60 min at 43 °C. Next, adjust pH=7 with 0.1mol / L sodium hydroxide solution and hydrochloric acid solution, centrifuge at 5000rpm at 25°C for 10min, take the supernatant, add 95% alcohol at 4°C at a ratio of 1:4 (V / V) The solution was stirred for 1 min and mixed well. Centrifuge again at 5000 rpm for 10 minutes at 25°C and discard the supernatant. The obtained precipitate was washed with a small amount of deionized water, and after removing the surface alcohol, the precipitate was dissolved with 0.1 mol / L PBS solu...
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