Aspergillus parasiticus and applications thereof in preparation of nitrite reductase, nitrite reductase gene and genetically engineered bacterium
A technology of parasitic Aspergillus and nitrite, applied in the field of microorganisms, can solve the problems of unsuitable breeding water and food treatment, low efficiency, secondary pollution, etc., and achieve fast and reliable degradation, good degradation effect, high efficiency and low energy consumption.
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Embodiment 1
[0031] Example 1. Screening, cultivation, identification and performance testing of Aspergillus parasitic strain JFS
[0032] 1. Screening of Aspergillus parasitic strain JFS:
[0033] (1) Material
[0034] a. Samples: 20 samples of water, soil, dead wood, rabbit dung and sheep dung collected from Chengdu, Sichuan, Yibin, and Chongqing Rongchang.
[0035] Sample processing and storage: The collected soil samples, dead wood, rabbit dung and sheep dung were all dried in a cool and dry place immediately after being collected, and stored in a clean kraft paper envelope after drying. The water sample is used directly after collection (fresh water is used).
[0036] b. Medium:
[0037] Nitrite selection medium (unit g / L):
[0038]
[0039] Cha's medium (unit g / L):
[0040] All the above-mentioned media are prepared in 1×10 5 Sterilize for 25 min under Pa.
[0041] c. Reagents and instruments:
[0042] Reagents: potassium ferrocyanide, zinc acetate, p-aminobenzenesulfonic acid, naphthalene ethyl...
Embodiment 2
[0119] Example 2. Application of Aspergillus parasiticus in the preparation of nitrite reductase gene
[0120] The preparation steps of nitrite reductase gene are as follows:
[0121] (a) Transfer the strain JFS from Cha's medium slant to Cha's plate or culture on Cha's slant at 30°C for 3-7 days, or transfer to Cha's seed medium at 30°C, 150r / min After culturing for 3 to 8 days, centrifuge or filter to collect bacteria and sporophytes.
[0122] (b) DNA extraction of the collected bacteria and sporophytes: the genomic DNA of strain JFS is extracted.
[0123] (c) Design degenerate primers based on the conserved regions of the amino acid sequence of nitrite reductase of various organisms in the Genbank protein database, and use the genomic DNA of strain JFS as a template to amplify the DNA fragment of nitrite reductase in strain JFS, Then sequence. The specific gene preparation can use the existing technology, which will not be repeated here.
[0124] In the preparation of the nitrite ...
Embodiment 3
[0125] Example 3 Application of Aspergillus parasiticus in the preparation of nitrite reductase
[0126] The strain JFS was transferred from the Cha's medium slant to Cha's seed medium. After culturing at 30°C and 150r / min for 2 days, it was transferred to the fermentation medium at 30°C, 150r / min with an inoculum of 3-10%. Cultivate for 3-9 days, centrifuge or filter, collect bacteria and sporophytes, rupture the cell wall of strain JFS with ultrasonic or liquid nitrogen grinding or glass bead grinding or use the above three methods at the same time, and then extract, Salting out, chromatography and other methods to purify nitrite reductase. The specific preparation method of nitrite reductase can adopt the existing technology, which will not be repeated here.
[0127] The Aspergillus parasitica of the present invention is used in the preparation of nitrite reductase. Because the Aspergillus parasitica of the present invention is easy to cultivate and has low cultivation cost, th...
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