Biological activator for reinforcing nitrogen fixing capacity of nodule bacteria
An indigenous root nodule and biological source technology, applied to biocides, microorganisms, animal repellents, etc., can solve the problems of low nitrogen fixation capacity, rhizobia agent invasiveness, low nodulation rate, etc., to achieve increased iron content, The effect of increasing the fresh dry weight and nitrogen fixation activity of root nodules and improving product quality
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Embodiment 1
[0019] Example 1 Preparation Example
[0020] (1) Trichoderma harzianum strain (Trichoderma harzianum) T216 parent species slant culture: adopt test tube PDA slant medium culture;
[0021] (2) Trichoderma seed shake flask culture, medium formula: soluble starch 30g, glucose 20g, peptone 5g, KH2PO4 1g, MgSO4 7H2O 0.5g, CaCO3 0.25g, (NH4)2SO4 2g, water 1000mL, pH6.9, Divide into 500mL Erlenmeyer flasks with a liquid volume of 200mL, sterilize at 115°C for 20 minutes, transfer the parent species to shake flasks under aseptic conditions, and culture at 27±1°C at 150 rpm for 60 Hours, get the seeds, standby; fermenter fermentation, access fermenter by 10% (V / V) inoculum size, carry out controlled fermentation, fermentation control parameters are: temperature control, divided into two stages, fermentation first stage bacteria Body culture stage 0-72 hours, 26-28 °C, fermentation second stage metabolite production 72-100 hours, 23-25 °C; ventilation (V / V): 0-20 hours: 1:0.6; 20-40...
Embodiment 4
[0045] The influence of embodiment 4 biological source T216 activators on the biological characteristics of indigenous rhizobia
[0046] (1) Acquisition of indigenous rhizobia
[0047] Collect cowpea plants at the early flowering stage grown under natural conditions in the field, pick off fresh, plump, and large root nodules on them, rinse them with tap water, soak them in 75% alcohol for 1 minute, rinse them with sterilized water for 3 times, and then put them Disinfect the surface in 0.1% mercuric chloride solution for 5 minutes, rinse with sterilized water for several times, put the nodules into a sterilized mortar filled with a small amount of sterilized normal saline (8.5 grams of sodium chloride in 1 liter of water) , use a glass rod to crush the root nodule; use an inoculation loop to dip the root nodule sap and draw a line on a plate containing Congo red Y.E.M. Rhizobia colonies, and the colonies were purified, cultivated and identified.
[0048] The composition of t...
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