Hylotelephium erythrostictum rhizosphere cadmium-resistant Cupriavidus sp., and screening method and applications thereof
A technology of cadmium-resistant and copper-loving bacteria, which is applied to the cadmium-resistant strain of Sedum rhizosphere, copper-loving bacteria, can solve problems such as harming human health.
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Embodiment 1
[0025] Example 1 Isolation of sedum rhizosphere cadmium-resistant strain Cupriavidus sp.BCd1
[0026] Materials and Methods
[0027] 1. Medium
[0028] Bacterial culture medium: beef extract 3g, peptone 10g, NaCl 5g, distilled water 1000mL, pH7.0.
[0029] Prepare screening medium: the basic medium is 1000ml of bacterial culture medium, add 10ml of trace element solution and vitamin solution, sterilize at 121°C for 20min, cool to about 70°C, add cadmium solution mother liquor, so that the cadmium content in the medium is 10mg· L -1 . Incubate at 37°C.
[0030] The trace element solution is: MnSO 4 0.01g, ZnSO 4 0.05g, H 3 BO 3 0.01g, CaCl 2 0.01g, dilute to 1L, and store at 4°C in the dark.
[0031] The vitamin solution is: creatine 0.025g, ascorbic acid 0.025g, riboflavin 0.025g, citric acid 0.02g, dilute to 1L, and store in the dark at 4°C.
[0032] Cadmium solution mother liquor: CdSO 4 Formulated as Cd 2+ The concentration is 200mg·ml -1 The mother liquor...
Embodiment 2
[0035] The bacterial species identification of embodiment 2 bacterial strain BCd1
[0036] 1. Genomic DNA extraction
[0037] The above-mentioned strain BCd1 was mass-cultured according to conventional technical means, and then its genomic DNA was obtained.
[0038] 2. Identification method of 16S rDNA of strain BCd1
[0039] 2.1 PCR amplification, sequencing and phylogenetic tree construction of 16SrDNA of strain BCd1
[0040] 2.1. PCR amplification of 116S rDNA gene sequence
[0041] The primers at both ends of the amplified 16S rDNA gene sequence are universal primers: forward primer BSF8 / 20: 5'-AGAGTTTGATCCTGGCTCAG-3' (SEQ ID NO: 1) and reverse primer BSR1541 / 20: 5'-AAGGAGGTGATCCAGCCGCA-3' (SEQ ID NO: 2). The PCR reaction system was 50 μl, and the reaction conditions were denaturation at 94°C for 5 minutes; followed by 35 cycle reactions: denaturation at 94°C for 45 s, annealing at 50°C for 45 s, and extension at 72°C for 90 s; then extension at 72°C for 10 min, and fi...
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