Specific strain and application thereof
A technology of Pseudomonas chloropinus and Aspergillus niger, applied in the field of microorganisms, can solve the problems of high industrialization cost, weak conversion production capacity, and low production efficiency
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Embodiment 1
[0070] Embodiment 1 Aspergillus niger CFFSH005 strain identification
[0071] Aspergillus niger strain CFFSH005 was isolated from the root soil of watermelon in Nanhui, Pudong New District, Shanghai.
[0072] Aspergillus niger CFFSH007 grows on potato medium, the mycelia are colorless at the initial stage, and dark brown to nearly black when mature. Observing under a microscope after taking the mycelia for staining, the mycelia are separated and have black spherical sporangia. According to K.B.Raper and D.I.Fennell "Aspergillus" (The Genus Aspergillus, 1965), the strain has typical characteristics of Aspergillus niger. Aspergillus niger CFFSH005 was deposited in the China Center for Type Culture Collection on December 20, 2016, and the preservation number is CCTCC NO:M 2016767
Embodiment 2
[0073] Example 2 Identification of Pseudomonas chlororaphis CFFSH007 and Pseudomonas chlorophis CFFSH008 strains
[0074] Two strains of Pseudomonas chloropinus were isolated from plant roots, identified by 16s rDNA, and the general primers were synthesized by Suzhou Jinweizhi Biotechnology Co., Ltd. The 27F / 1492R sequence is as follows:
[0075] 27F (5'→3'): AGAGTTTGATCMTGGCTCAG
[0076] 1492R (5'→3'): TACGGYTACCTTGTTACGACTT
[0077] The colony of Pseudomonas chlororaphis CFFSH007 was taken, and its 16s rDNA was subjected to colony PCR with universal primers 27F and 1492R to obtain a full-length 1413bp DNA sequence, which is shown in sequence 1 of the gene sequence attached table. Using NCBI's Sequence 1 was compared, and the results showed that the similarity between Pseudomonas chlororaphis CFFSH007 and the 16s rDNA of Pseudomonas chlororaphis ATCC 13985 was 100% (1413 / 1413); at the same time, the similarity with the 16s rDNA of Pseudomonas chlororaphis Lzh-T5 was 100% (...
Embodiment 3
[0079] Example 3 Screening of strains producing vanillic acid
[0080] (1) Isolation of strains
[0081] Take 50g fresh root soil samples of watermelon field in Nanhui area, Shanghai, disperse and mix with 100mL sterile normal saline, take 100uL for gradient dilution, spread on the prepared sieving agar plate, and place in a 30°C incubator Incubate until a single colony is formed. The formula of the sieving agar plate culture medium is: 2% (w / v) agar powder, 5% (w / v) glucose, 0.5% (w / v) ferulic acid, 1% yeast powder, 0.3% pancreatic Peptone, pH 7.0. The formed single colonies were transferred and preserved, and the strains were identified.
[0082] (2) Identification of vanillic acid transformation ability of wild Aspergillus niger
[0083] Select to obtain 10 strains of Aspergillus niger strains from soil samples, get the mature spores cultivated in the potato dextrose solid medium plate for 7 days, and inoculate them in 90mL culture potato dextrose liquid medium (potato ...
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