Extract of sparassis crispa MH-3 bacterial strain and method for preparing the same and use thereof
A hydrangea and extract technology, applied in the field of hydrangea MH-3 strain NIBH FERMP-17221 extract, can solve the problems of difficult artificial cultivation and slow growth
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Embodiment 1
[0044] The hydrangea MH-3 strain was pulverized into powder, and a weight ratio mixture of chloroform:methanol:water=200:200:60 was prepared, and 25 g of the pulverized dry powder was subjected to degreasing treatment for 2 days at room temperature.
Embodiment 2
[0046] After obtaining the extract (test sample 2) in Example 1, Example 2 was carried out. 500 ml (4°C) of 10% NaOH alkaline water to which 5% urea was added was added to the residue obtained in Example 1, and extraction treatment was performed for 2 days to obtain an extract (test sample 3). After dialysis, ethanol precipitation, dehydration, and drying were performed to obtain 4.93 g of cold alkali extract B.
Embodiment 3
[0048]After obtaining the extract (test sample 3) obtained in Example 2, Example 3 was carried out. 500 ml (65 degrees) of hot alkaline water of 10% NaOH to which 5% urea was added was added to the residue obtained in Example 2, and extraction treatment was performed for 1 hour to obtain an extract (test sample 4). After dialysis, ethanol precipitation, dehydration, and drying were performed to obtain 1 g of hot alkali extract C.
[0049] The solid matter after the degreasing treatment was air-dried, put into an autoclave, added 500 ml of hot water, and subjected to hot water extraction for 2 hours to obtain an extract (test sample 1). The residue after extraction was put into an autoclave, 500 ml of water was added, and hot water extraction was further performed for 2 hours to obtain an extract (test sample 2). Mix the extracts obtained by hot water extraction (test samples 1 and 2), add a large amount of ethanol (200ml), centrifuge at 5000rpm for 5 minutes to precipitate, a...
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