Preservation method of denitrifying bacteria
A technology of denitrifying bacteria and preservation method, applied in the direction of preservation of microorganisms, etc., can solve problems such as difficulty in meeting large-scale production requirements and low efficiency, and achieve the effects of reducing metabolic rate and prolonging preservation time.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0023] Take 100mL of the denitrifying bacteria liquid independently isolated and cultivated in the laboratory (bacterial quantity: 2.6×10 9 cfu / ml, using the plate counting method, the same below), put it into a 5L square small-mouth plastic bucket for storage, add 4.9L of phosphate buffer, add FeSO 4 , MgCl 2 , MnCl 2 0.02g each and carry out uninterrupted aeration to maintain the dissolved oxygen above 5mg / L. The formula of phosphate buffer is: 0.06mol / L Na 2 HPO 4 Add 1.9L, 0.06mol / L of KH 2 PO 4 Add 3L. The mixture was stored at room temperature. After 2 weeks and 1 month of preservation, the preserved bacterial liquids were respectively taken and spread on a flat plate, and the statistical survival rates were 97.5% and 94.7%, respectively.
Embodiment 2
[0025] Take 5L of the denitrifying bacteria liquid independently isolated and cultivated in the laboratory (bacteria quantity: 2.6×10 9 cfu / ml), put into a 5L square small-mouth plastic barrel for storage, add 4.9L of phosphate buffer, and add FeCl 2 , MgSO 4 , MnCl 2 0.02g each, and carry out uninterrupted aeration to maintain its dissolved oxygen above 4mg / L. The formula of phosphate buffer is: 0.06mol / L Na 2 HPO 4 Add 1L, 0.06mol / L of KH 2 PO 4 Add 3.9L. The mixture was stored at room temperature. After 2 weeks and 1 month of preservation, the preserved bacterial liquids were respectively taken and spread on a flat plate, and the statistical survival rates were 94.1% and 89.0%, respectively.
Embodiment 3
[0027] Take 5L of the denitrifying bacteria liquid independently isolated and cultivated in the laboratory (bacteria quantity: 2.6×10 9 cfu / ml), put into a 5L square small mouth plastic bucket for storage, add 4.9L KH 2 PO 4 -NaOH buffer with addition of FeSO 4 , MgSO 4 , MnCl 2 0.05g each and carry out uninterrupted aeration to maintain the dissolved oxygen above 8mg / L. K H 2 PO 4 -NaOH buffer formula is: K of 0.03mol / L 2 HPO 4 Add 4.4 L, and add 0.5 L of 0.03 mol / L NaOH. The mixture was stored at room temperature. After 2 weeks and 1 month of preservation, the preserved bacterial liquids were respectively taken and spread on a flat plate, and the statistical survival rates were 82.6% and 78.5%, respectively.
PUM
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