Silver nanometer material and biological preparation method and application thereof
A bio-preparation and silver nanotechnology, applied in the field of bio-preparation of silver nanomaterials, can solve problems such as difficult to control slow-release, secondary pollution, poor stability, etc., to achieve good application prospects, good antibacterial effect, particle size Narrow distribution effect
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Embodiment 1
[0039] The biological preparation of silver nanomaterials, the preparation process is as follows:
[0040] Fusarium solani D07 strain activation→seed culture solution→fermentation culture→suction filtration to obtain mycelium→mycelia culture in sterile deionized water→suction filtration to obtain filtrate→add AgNO 3 Reaction → material acquisition.
[0041] Concrete preparation process comprises the following steps:
[0042] (1) Take the endophytic fungal strain Fusarium solani D07 of Dendrobium officinale, pick a small amount of hyphae with an inoculation needle under sterile conditions, insert it into a sterilized solid PDA medium test tube, and activate it at 28±1°C 72 hours;
[0043] (2) Take the strain after activation and culture, transfer it into the sterilized liquid PDB seed medium under aseptic conditions, and cultivate it on a shaker at 28±1° C. and 120 rpm for 72 hours to obtain the seed liquid;
[0044] (3) Under sterile conditions, insert 10v% (volume percentage...
Embodiment 2
[0054] The nanomaterial obtained in Example 1 and Comparative Example 1 is carried out to the test observation of antibacterial activity, and the evaluation of antibacterial activity adopts the filter paper method, and the flow process is as follows:
[0055] Activation of pathogenic bacteria strains → seed liquid cultivation → plate coating inoculation → silver nano filter paper sheet inoculation → cultivation → antibacterial effect observation.
[0056] Bacteriostatic activity observation specifically includes the following steps:
[0057] (1) Take 7 kinds of common pathogenic bacteria selected for use: Escherichia coli, Staphylococcus aureus, Bacillus subtilis, Salmonella, Bacillus cereus, Candida tropicalis and Alcaligenes strains, under sterile conditions, use Pick up a small number of colonies with the inoculation needle, insert them into a test tube of sterilized beef extract peptone medium (solid state), and activate at 37±1°C for 24 hours;
[0058] (2) Take the strai...
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