Brevibacterium aureum AN3 and use thereof in degrading malachite green and other dyes
A malachite green, Brevibacterium technology, applied in bacteria, microorganism-based methods, microorganisms and other directions, can solve the problems of incomplete degradation, no discovery of Brevibacterium aureus degrading dyes, etc., to achieve improved efficiency, good market application prospects, improved The effect of ecological environment quality
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0026] Take 5mL of activated sludge from an anaerobic baffle reactor system used by a research institute in Guangzhou to treat printing and dyeing wastewater in 50mL of dye medium (1.0g of yeast extract per liter of medium, (NH4) 2 SO 4 2.5g, KH 2 PO 4 13.3g, Na 2 HPO 4 21.6g, and add triphenylmethane, so that the dye concentration in the medium is 50mg / L, the rest is water), 30 ℃ static culture, observe the decolorization of the dye, when the dye in the culture medium is basically completely decolorized , transferred to another fresh same medium with 10% inoculum size, and repeated several times until the decolorization time was significantly shortened, and the culture solution was properly diluted and evenly spread on the LB solid medium (containing Peptone 10g / L, yeast extract 5g / L, NaCl 10g / L, agar strip 2%, pH7.0), cultured at 30°C for 24h, picked a single colony for isolation and purification, and isolated and purified the single colony with LB The liquid medium (wi...
Embodiment 2
[0028] Add Na to 200mL deionized water 2 HPO 4 ·7H 2 O 2.56g, KH 2 PO 4 0.6g, NaC 0.1g, NH 4 Cl 0.2g, malachite green GR (C.I.42000) 0.01g, sterilized at 211°C for 20 minutes as dye culture solution. Inoculate the slant surface of the bacterial strain AN3 obtained in Example 1 into LB liquid medium, activate the thalline on a shaker at 30°C and 150r / min, and make the number of bacteria reach 10 8 Order of magnitude, inoculate the activated bacteria solution in the dye culture solution with an inoculation amount of 1 / 10, and culture it statically at 30°C, observe the color change of the culture solution, take 10mL of the dye culture solution every 30 minutes and centrifuge at 6000r / min to remove the bacteria , using a DU640 ultraviolet spectrophotometer (BECKMAN) to measure the absorbance value of malachite green GR (C.I.42000) in the dye culture solution at 617nm, and taking the dye culture solution without adding bacteria as a control, the degradation rate of the dye was...
Embodiment 3
[0030] Add Na to 200mL deionized water 2 HPO 4 ·7H 2 O 2.56g, KH 2 PO 4 0.6g, NaCl 0.1g, NH 4 Cl 0.2g, crystal violet (C.I.42555) 0.01g, sterilized at 211°C for 20 minutes as a dye culture solution. Inoculate the slant surface of the bacterial strain AN3 obtained in Example 1 into LB liquid medium, activate the thalline on a shaker at 30°C and 150r / min, and make the number of bacteria reach 10 8 Order of magnitude, inoculate the activated bacterial solution in each dye culture solution with an inoculation amount of 1 / 10, culture at 30°C, observe the color change of each culture solution, take 10mL dye culture solution every 30 minutes and centrifuge at 6000r / min Bacteria were removed, and the absorbance of crystal violet (C.I.42555) in the dye culture solution was measured at 590nm with a DU640 ultraviolet spectrophotometer (BECKMAN), and the dye degradation rate was calculated using the corresponding dye culture solution without bacteria as a control. The obtained stra...
PUM
Property | Measurement | Unit |
---|---|---|
clearance rate | aaaaa | aaaaa |
clearance rate | aaaaa | aaaaa |
clearance rate | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com