Debaryomyces hansenii strain and application in preparation of fruit fresh-keeping agent
A technology of yeast and antistaling agent, which is applied in the application field of preparing fruit antistaling agent, can solve the problems of destroying ecological balance, endangering human health, polluting the environment, etc., and achieves the effects of reducing preservation cost, low cost and prolonging storage time
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Embodiment 1
[0036] Embodiment 1 Debaryomyces hansenii 'NDB-001'
[0037] The applicant isolated and screened a yeast strain from mangoes in Guangdong. The colonies of this strain on different culture plates are relatively similar in shape, with single cells being oval or round, and the cells are polygonal buds. The colony formed on the plate is oval, milky white, smooth, uniform and viscous in texture, with a high central bulge and umbilicus shape, and the edges of the colony are neat. Ascospores can be formed on the medium, and the cells mate with them to form ascus, and one ascus produces 1-4 spherical ascospores. The above morphological characteristics are similar to those of Debariae spp. described in the literature, and the ITS1 nucleotide sequence of the strain is shown in SEQ ID NO.1; therefore, the strain is named Debariea hansenii 'NDB -001 'Debaryomyceshansenii'NDB-001'. The yeast strain was deposited in the China Center for Type Culture Collection on May 7, 2020. The deposit ...
Embodiment 2
[0040] Embodiment 2: the preparation of fruit fresh-keeping material
[0041] In order to obtain fresh-keeping substances, the present invention shakes and cultures the yeast for 48 hours (YPD liquid medium, culture temperature 20-30° C.), and centrifuges at low temperature (4° C.) to collect the bacteria. Suspend the bacterial pellet with sterile water to make a yeast suspension and adjust the concentration to 1x10 8 cfu / mL is made into fresh-keeping substances.
Embodiment 3
[0042] Embodiment 3: Indoor plate inhibition assay of pathogenic bacteria by fruit fresh-keeping substances
[0043] In order to test the effectiveness of the fresh-keeping material on the growth inhibition of pathogenic bacteria, the present invention takes the fresh-keeping material and places it in half of the two-compartment petri dish. The other half was poured into the culture medium to cultivate pathogenic bacteria, placed in a constant temperature incubator at 25°C, cultivated in the dark, observed and measured the colony diameter with the cross method. Calculate the inhibitory rate of the fresh-keeping material to the pathogenic bacteria by the following formula:
[0044]
[0045] The specific plan is as follows:
[0046] (1) Preparation of test strains: inoculate Botrytis cinerea cultured for about 7 days in the center of one of the two-compartment petri dishes containing PDA medium; pour into the other compartment for cultivating yeast YPD medium.
[0047] (2)...
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