Bacillus licheniformis-containing composite microbial inoculum for degrading straw and application thereof
The technology of Bacillus licheniformis and compound bacterial agent is applied in the field of compound bacteria, which can solve the problems of unreasonable development of straw resources, limited utilization of microbial degradation straw, and poor straw degradation effect, so as to reduce the incidence of diseases and insect pests and inhibit growth. Effects of reproduction, dark green leaves
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Embodiment 1
[0019] The mutagenic screening of embodiment 1 verrucous Myromyces
[0020] (1) Morphological identification and screening
[0021] The soil in the forest area of Changbai Mountain Nature Reserve was collected and cultivated on PDA medium by conventional methods. The mycelium of the strain was white flocculent at first, and grew divergently towards the periphery. After 8 days of culture, the color of conidia continued to deepen, and glue dots appeared; after 10 days of culture, the colony was in the shape of concentric rings, the conidia showed black glue spots, and the back of the colony appeared Hazel radial folds.
[0022] Use a puncher to get a 1cm-diameter bacterial block, inoculate it on an aniline blue selective medium, and culture it in an aerobic incubator at 30°C for 10 days, observe the fading of aniline blue, and select a strain with a fast fading rate and strong ability as candidate strains.
[0023] At the same time, in order to directional screen lignin-deg...
Embodiment 2
[0029] The low-temperature acclimatization of embodiment 2 bacterial strains
[0030] (1) Enrichment culture strains
[0031] Inoculate the strain into a Erlenmeyer flask filled with 150mL of PDA medium, add filter paper pieces with a length of 5cm and a width of 2cm, incubate at a constant temperature at 30°C for 1 hour and mix evenly, and make 10 -1 -10 -9 For dilution, 1 mL of each dilution was inoculated in PDA medium with filter paper as the only carbon source, and static enrichment culture was carried out at 28°C for 4 generations. Screen out the materials with short breakage time and high degree of ulceration of filter paper. PDA medium: potato 200g / L, glucose 20g / L, agar 15g / L
[0032] Natural corn stalk powder shaker culture: Weigh 5 g of the strain source sample and add it to 100 mL corn stalk powder medium with natural corn stalk powder as the only carbon source (replacing the filter paper in the PDA medium with corn stalk powder, culture at 28°C and 150 rpm On ...
Embodiment 3
[0045] The preparation of embodiment 3 composite bacterial agents
[0046] Cellulase-producing Paenibacillus, xylanase-producing Alternaria, laccase-producing Mycobacterium verrucosus, lignin-peroxidase-producing Bacillus colloid, manganese-peroxidase-producing Lys Bacillus licheniformis and Bacillus licheniformis were activated in a conventional manner and cultured until the number of viable bacteria in the bacterial liquid reached 2.0×10 8 individual / mL.
[0047] Mix the bacterial solution according to the following mass ratio: 20% of Paenibacillus cellulase-producing bacteria, 10% of Alternaria xylanase-producing bacteria, 20% of Laccase-producing Mycobacterium verrucosus, lignin peroxidase glue 10% of Bacillus plasmodia, 10% of Manganese peroxidase-producing Leysia lanceolata, and 30% of Bacillus licheniformis, and fully stirred and mixed to obtain a mixed bacterial liquid.
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