Bacillus amyloliquefaciens producing lipopeptide to promote fungi apoptosis and lipopeptide prepared by the same and use
A technology for dissolving amyloid spores and fungi, applied in applications, peptides, bacteria, etc.
Patent Information
- Authority / Receiving Office
- CN · China
- Current Assignee / Owner
- Publication Date
- 2009-04-29
- Estimated Expiration
- Not applicable · inactive patent
Smart Images
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Abstract
Description
technical field
[0001] The invention belongs to the technical field of agricultural microbiology, and specifically relates to the isolation and screening of a strain of Bacillus amyloliquefaciens producing lipopeptides that promote fungal apoptosis and the preparation of active substances. The invention also relates to some technical fields of biochemistry and molecular biology. Background technique
[0002] Many bacillus, such as Bacillus subtilis (Bacilus subtilis), Bacillus mycoides (B.mycoides) and Bacillus amyloliquefaciens (B.amyloliquefaciens), can inhibit the growth of many plant pathogenic fungi and human pathogenic fungi. Many of these antifungal substances have been identified as having the characteristics of cyclic lipopeptide surfactants. These lipopeptides can inhibit the growth of many fungi, including Aspergillus (Aspergillus), Fusarium (Fusarium), Rhizoctonia (Rhizoctonia) and some yeasts (Candida). The antitumor activity of some lipopeptides has also rece...
Examples
Embodiment 1
[0035] 1. Screening and isolation of Bacillus amyloliquefaciens:
[0036] Several rice plants at the tillering stage were taken from the paddy fields of Huazhong Agricultural University in Wuhan, Hubei Province, China, and the roots were separated after washing. Rinse the outer surface of the rice root with tap water, then rinse it three times with sterile water, then soak it in 70% ethanol for 30 seconds, take it out, rinse it three times with sterile water, and cut the rice root into about 1mm with sterile scissors Then put the fragments of the same size on PDA medium (containing 200g potato boiled liquid, 20g glucose, 20g agar, add distilled water to 1L) and incubate at 28°C for 48h. The isolated bacteria were cultured with PD liquid medium (containing 200g potato boiled liquid, 20g glucose, and distilled water to 1L) at 28°C, shaken at 180rpm for 48h, centrifuged, and the supernatant was collected and filtered through a 0.22μm membrane After filtering, mix it with PDA med...