Penicillium oxalicum for reducing hexavalent chromium and screening method thereof
A Penicillium oxalate, screening method technology, applied in the field of microorganisms, can solve the problems of limited application, difficult to tolerate high salt conditions, poor adaptability and the like
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Embodiment 1
[0019] Embodiment 1: the screening method of the Penicillium oxalicum of a strain reduction Cr (VI)
[0020] 1.1 Make a PDA plate containing Cr(VI): Weigh 20g of potatoes and add them to 100ml of water, boil for 30min, filter through double-layer gauze, replenish water to 100ml, add 1g of glucose, 1.5g of agar, sterilize at 115°C for 20min, cool until it is not hot, Add potassium dichromate solution sterilized by a 0.22 μm sterile filter head to make the culture medium contain 300 mg / L of Cr(VI), and pour the plate in a sterile operating table.
[0021] 1.2 Make Cr(VI)-containing liquid medium: Weigh 20g of potatoes and add to 100ml of water, boil for 30min, filter through double-layer gauze, replenish water to 100ml, add 1g of glucose, sterilize at 115°C for 20min, cool until it is not hot, add 0.22 Potassium dichromate solution sterilized with a μm sterile filter head, so that the medium contains 300 mg / L of Cr(VI).
[0022] 1.3 Collection: Place the Cr(VI)-containing PDA p...
Embodiment 2
[0026] Example 2: Morphology, Carbon Source Utilization, and Molecular Biological Identification of Bacterial Strain SL2
[0027] The detection and identification of strain SL2 was entrusted to the China Center for Type Culture Collection, and the results are as follows:
[0028] 2.1 Morphological features
[0029] Colonies of strain SL2 were developed and velvety. dark green( figure 1 ). Conidia chain integrated cylindrical, conidia oval P ( figure 2 ).
[0030] 2.2 Characteristics of carbon source utilization
[0031] The utilization of 95 carbon sources by SL2 was detected by biolog FF plate, and the results showed that it could utilize 56 of them.
[0032] Table 1 Carbon source utilization of SL2 strain
[0033] Test items result Test items result A1 water B7 D-galactose + A2 Tween 80 + B8 D-galacturonic acid + A3 N-acetyl-galactosamine - B9 Gentiobiose + A4 N-acetyl-glucosamine + B10 D-gluconic ...
Embodiment 3
[0041] Embodiment 3: Salt tolerance, Cr (VI) tolerance detection of bacterial strain SL2
[0042] Make the liquid PDA culture medium that contains NaCl concentration and be 0g / L, 20g / L, 100g / L. Press 10 4 cells / mL inoculated with SL2
[0043] For the spores, the culture system was placed in a shaker at 30°C and 200 rpm for shaking culture. The mycelia were filtered daily and weighed ( image 3 ). The results showed that SL2 had strong salt tolerance and could grow in PDA medium with NaCl concentration exceeding 100g / L.
[0044] Add potassium dichromate solution sterilized by filtration through a 0.22 μm filter membrane into the liquid PDA medium to prepare a PDA medium containing Cr(VI) at a concentration of 2000 mg / L. Press 10 4 The spores / mL were inoculated with SL2, and the culture system was shaken in a shaker at 30°C and 200 rpm. The mycelia were filtered daily and weighed ( Figure 4 ). The results showed that SL2 had strong tolerance to Cr(VI), and could grow ...
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