Heavy-metal-resisting microbial agent, preparation method and application thereof
A technology of microbial preparations and heavy metals, applied in the field of environmental biology, can solve problems such as rising, non-heavy metal indicators have not been improved, and water quality discharge standards cannot be met, and achieve the effect of low cost and high efficiency
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Embodiment 1
[0030] Collect 3 soil samples 3-10 cm below the surface layer polluted by heavy metals from different locations near the electroplating factory, carry out enrichment culture in shake flasks in the enrichment medium for 3 days, transfer culture for 3 times, and then dilute and plate in the separation medium , two single colonies were obtained after multiple isolations.
[0031] Two strains of bacteria were identified using the automatic bacterial identification system-Cell Fatty Acid Mapping Identification System (MIDI). After identification, the two strains were Acinetobacter calcoaceticus and Pseudomonas aeruginosa, and were preserved in the The General Microbiology Center of the China Committee for the Collection of Microbial Cultures is located at the Institute of Microbiology, Chinese Academy of Sciences, Datun Road, Chaoyang District, Beijing.
[0032] Acinetobacter calcium acetate is named Acinetobacter calcoacetcus (Acinetobacter calcoacetcus) HDD1, and the preservation...
Embodiment 2
[0035] Use beef extract peptone medium, the formula is beef extract 3g, peptone 10g, NaCl 5g, water 1000mL, pH7.4~7.6, medium contains Ni 2+ 50mg / L, Pb 2+ 20mg / L, Cr 6+ 10mg / L, Cu 2+ 10mg / L, Zn 2+ 500mg / L. Acinetobacter calcoacetcus (Acinetobacter calcoacetcus) with the preservation number CGMCC No.6820 and Pseudomonas aeruginosa (Pseudomonas aeruginosa) with the preservation number CGMCC No.6821 were respectively activated by slant culture at 28°C for 12 hours, and then in 500ml triangular The flask shaker was cultured separately, the culture time was 48 hours, and 3L of the bacterial liquid was obtained respectively; the 6L of the above-cultured bacterial liquid mixture was inoculated into a 20L solid fermenter, the inoculation amount was 30%, and the solid medium was composed of 50 parts of bran, corn 10 parts of core powder, 15 parts of soybean meal, 2 parts of starch, 2 parts of urea, 0.5 parts of sodium glutamate, 2 parts of ammonium sulfate, KH 2 PO 40.8 parts, th...
Embodiment 3
[0037] Use beef extract-peptone medium, the formula is beef extract 3g, peptone 10g, NaCl 10g, water 1000mL, pH7.4~7.6, medium contains Ni 2+ 50mg / L, Pb 2+ 20mg / L, Cr 6+ 10mg / L, Cu 2+ 10mg / L, Zn 2+ 100mg / L. The Acinetobacter calcoacetcus (Acinetobacter calcoacetcus) with the preservation number CGMCC No.6820 and the Pseudomonas aeruginosa (Pseudomonas aeruginosa) with the preservation number CGMCC No.6821 were respectively activated by slant culture at 28°C for 12 hours, and then in 500ml The Erlenmeyer flask shaker is cultured separately, and the culture time is 48h, and 3L of bacterial liquid is obtained respectively; 6L of the bacterial mixture cultured above is inoculated into a 20L solid fermenter, the inoculation amount is 30%, and the solid medium composition is in parts by weight: bran 50 parts, 10 parts of corn cob flour, 15 parts of soybean meal, 2 parts of starch, 2 parts of urea, 0.5 parts of sodium glutamate, 2 parts of ammonium sulfate, KH 2 PO 4 0.8 parts,...
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