Rhizomucor variabilis and its cultivation method, bacterial agent and application
A cultivation method and root hair technology, applied in the field of microorganisms, can solve problems such as short interval time, high multiple cropping index, incomplete straw decomposition, etc., and achieve high economic and social benefits, and rapid decay effects
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preparation example
[0057] This preparation example is used to prepare the fungal seed liquid used in the following examples.
[0058] The above-mentioned fungal liquid culture medium was sterilized at 121°C for 15 minutes, and then cooled to room temperature. The bacterium liquid of the Rhizomucor variabilis strain of 3 volume % is inserted in the above-mentioned sterilized fungal liquid culture medium of 200mL, at 150-240rpm, cultivate 5 days under the culture condition of 25-35 ℃, so that its spore quantity reaches 10 7 cells / mL to obtain the fungal seed solution.
Embodiment 1
[0060] This example is used to illustrate the degradation ability of Rhizomucor versicolor of the present invention to cellulose.
[0061] Test group: Add filter paper strips (1g in weight) to 100mL inorganic salt liquid medium in the Erlenmeyer flask, autoclave at 121°C for 15min, cool to room temperature, add 1mL of the fungal seed solution prepared in the above preparation example , and then cultured at 170rpm and 30°C for 5 days.
[0062] Blank control group: except that 1 mL of fungal seed liquid was replaced by 1 mL of fungal liquid culture medium, other operating conditions were the same as those of the test group.
[0063] Wherein, the composition of the inorganic salt liquid medium is 1.5% by weight of NH 4 NO 3 , 1.0 wt% KH 2 PO 4 , 1.0 wt% K 2 HPO 4 , 0.05 wt% MgSO 4 , pH 6.0-7.5.
[0064] Dry the cultures of the test group and the blank control group together with the Erlenmeyer flasks, and then weigh them respectively to obtain the difference between the w...
Embodiment 2
[0067] This example is used to illustrate the ability of Rhizomucor versicolor of the present invention to degrade lignin in water.
[0068] Test group: Take 100mL sodium lignosulfonate inorganic salt liquid medium, autoclave at 121°C for 15 minutes, cool to room temperature, insert 1mL of the fungal seed liquid prepared in the above preparation example, and then sterilize at 170rpm and 30°C cultured for 5 days.
[0069] Blank control group: except that 1 mL of fungal seed liquid was replaced by 1 mL of fungal liquid culture medium, other operating conditions were the same as those of the test group.
[0070] Take out a little of the five-day cultured liquid of the test group and the blank control group, centrifuge at 12,000 rpm for 10 min, and get the supernatant. The absorbance of the supernatant was measured at 280 nm by a UV spectrophotometer. Wherein, the absorbance value of the test group was 0.140, and the absorbance value of the blank control group was 0.697.
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