Highland bacillus altitudinis and application thereof in artificial ageing of tobacco leaves at upper part of flue-cured tobacco
A bacillus and highland technology, applied in the fields of agricultural microorganisms and tobacco aging, can solve the problems of poor usability and inferior quality of tobacco leaves, achieve the effects of reducing irritation and miscellaneous gas, improving aroma quality and aroma quality, and shortening the aging cycle
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Embodiment 1
[0022] Example 1: Isolation and breeding of Bacillus highlander D2.
[0023] Tobacco leaves from different origins (Hubei Province, Yunnan Province) stored naturally for 2 years in the warehouse of Wuhan Cigarette Factory, and flue-cured tobacco leaves that had not been artificially aged were cut into pieces with sterilized scissors, soaked in 100 mL of sterile water, Shake on a shaker at 200rpm for 30min, take 0.1mL after shaking evenly, and spread it on an LB plate (medium composition (g / L): peptone 10g, yeast powder 5g, sodium chloride 10g, dilute to 1000mL with distilled water; agar 15-20g / L, adjust the pH of the medium to 7.0-7.4), after 12 hours of cultivation, number the various colonies, inoculate them in LB liquid medium, cultivate them for 12 hours, and inoculate them on the starch plate with an inoculation needle Above (medium composition (g / L): soluble starch 2g, peptone 10g, yeast powder 5g, sodium chloride 10g, distilled water to 1000mL, adjust the pH of the medi...
Embodiment 2
[0030] Example 2: Identification of the morphological and physiological and biochemical characteristics of the Bacillus alboteria (CCTCC NO: M2011056) D2 strain.
[0031] Refer to the test method of George M.Garrity "Bergey's Manual of Systematic Bacteriology" Vol.VIII (1974 edition) to detect its Gram staining, cell size and shape, presence or absence of flagella and spores, growth temperature, pH range, NaCl Tolerance, catalase, H2S test, starch hydrolysis, cellulose hydrolysis, MR test, phenylalanine deamination, urease test, oxidase, gelatin liquefaction, tyrosine degradation, V-P test, and utilization of mannitol, Arabica Sugar, galactose, xylose, rhamnose, sucrose, inositol and citrate tests.
[0032]The results showed that the bacterium was Gram-positive, rod-shaped, with a size of 0.5 μm to 1.0 μm × 3.0 μm to 6.0 μm, spores terminal or subterminal, perinatal flagella, and able to move; the growth temperature was 27-45 ° C, pH4~9, NaCl tolerance 2%~6%; gelatin liquefac...
Embodiment 3
[0033] Example 3: PCR amplification and sequence determination of the 16S rRNA gene of Bacillus highlander D2 strain.
[0034] The specific steps are:
[0035] Inoculate the D2 strain of Bacillus upaliensis (preservation number CCTCC NO: M2011056) in LB medium, 200rpm, 37°C shaking culture for 12 hours, centrifuge to collect the bacteria, add lysozyme after suspension, use CTAB method and SDS method to break the wall, use Genomic DNA was extracted with phenol-chloroform-isoamyl alcohol, and the 16S rRNA gene was detected with 16S rRNA universal primer forward primer 27F (5'-AGAGTTTGATCCTGGCTCAG-3') and reverse primer 1492R (5'-GGTTACCTTGTTACGACTT-3'). PCR amplification, the amplified product was submitted to Shenzhen Huada Gene Research Institute for sequencing. The PCR conditions are: 94°C, 5min; 95°C, 40s, 55(-1°C / cycle)°C, 30s, 72°C, 25s, 6 cycles; 95°C, 40s, 55°C, 45s, 72°C, 1.5min, 30 cycles; 72°C, 5min, 10°C, 5min. The length of the PCR product is 1465bp, and its simi...
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