Gene chip and method of identifying highly effective ore leaching strain utilizing the same
A technology of gene chips and bacteria strains, which is applied in the field of rapid screening of highly efficient ore leaching strains, can solve the problems of heavy workload, poor reliability, and long time for screening of ore leaching strains
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Embodiment 1
[0015] Embodiment 1: Preparation of gene chip of the present invention
[0016] The present invention firstly constructs a whole-genome gene chip of type A.f strain ATCC 23270, which contains all 3217 genes of the strain. The genomic DNA of 5 strains of highly active A. f bacteria was hybridized with the constructed gene chip, and it was found that they jointly contained 320 genes related to ferrous and sulfur oxidation and resistance. The RNA of 5 highly active bacteria was further extracted and hybridized with the gene chip. Through the analysis of the gene expression map, it was found that a total of 135 genes were highly expressed in different highly active bacteria among the 320 characteristic genes, thus finding the genes directly related to the leaching performance. There are 135 functional genes, and the 135 genes are listed in Tables 1 to 4. They include 72 genes related to energy metabolism such as ferrous iron and sulfur oxidation, 18 genes related to high temperatu...
Embodiment 2
[0020] Embodiment 2: use the gene chip of the present invention to identify high-efficiency ore leaching bacterial strains
[0021] (1) Cultivation of the sample strain to be tested, DNA or RNA extraction and fluorescent labeling
[0022] Obtain a strain A.f bacterium (CMS05 bacterial strain) from certain copper ore isolation as the sample strain to be tested, carry out the expansion culture of sample, use 9K medium, every liter of medium contains 3g (NH 4 ) 2 SO 4 , 0.1g KCl, 0.5g K 2 HPO 4 , 0.5g MgSO 4 ·H 2 O, 0.01g Ca(NO 3 ) 2 , 44.3g FeSO 4 ·7H 2 O, 5g elemental sulfur, and add 2000g of lead acetate, 100g of silver nitrate, 0.4g of mercury sulfate, and 2500g of copper sulfate in the middle of the logarithmic growth period of the sample bacteria (the concentration of bacteria is not less than 107 / mL, and the total amount is not less than 2L). , Arsenic trioxide (As 2 o 3 ) 100 g, collect the bacterial liquid after culturing for 1 hour. DNA or RNA is extracted ...
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