Dendrobium officinale kimura et migo endophytic fungi strain NT66G01 and application thereof
A technology of NT66G01 and Dendrobium candidum, applied in the field of microorganisms, can solve the problems of large market demand, no available wild resources, resource depletion, etc., and achieve the effects of increasing yield, promoting growth, and significant application value
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Embodiment 1
[0022] The endophytic fungal strain NT66G01 of Dendrobium officinale according to the present invention was preserved in the China Center for Type Culture Collection (Wuhan University, Luojia Mountain, Wuchang, Wuhan City, Hubei Province, zip code 430072) on July 9, 2014, and the preservation number is CCTCC NO.M2014334 ; The genome 18s rDNA base sequence of this strain is shown in SEQ ID No.1.
[0023] The solid culture characteristic of described Dendrobium officinale endophytic fungal strain NT66G01 is:
[0024] When cultured on potato dextrose agar (PDA) medium at 28±1℃, the aerial hyphae were colorless at first and gradually turned white; the colonies were white fluffy, the mycelia were more developed, and the place near the medium was lavender for a long time. The white on the back slowly turns reddish-brown.
[0025] The liquid culture characteristic of described Dendrobium officinale endophytic fungal strain NT66G01 is:
[0026] a) Medium PDA, cultured in shake flask...
Embodiment 2
[0032] 1) get Dendrobium officinale endophytic fungal strain NT66G01 strain of the present invention, under aseptic conditions, pick a small amount of mycelium with an inoculation needle, insert a sterilized solid PDA medium test tube, and activate the culture at 28 ± 1 °C 72 hours;
[0033] 2) get the bacterial classification after the activation culture, under aseptic conditions, transfer into the sterilized liquid PDA seed medium, cultivate at 28 ± 1 ° C, 140 rpm shaker for 72 hours to obtain seed liquid;
[0034] 3) Under sterile conditions, insert into 500mL liquid PDA medium according to the inoculation amount of 10V% (volume percentage), and cultivate at 28±1°C, 140rpm shaker for 7 days;
[0035] 4) vacuum-filtering the fermentation broth, combining the grinding liquid of mycelium and liquid nitrogen with the filtrate and sterilizing at 121° C. for 20 minutes to obtain fungal elicitors;
[0036] 5) insert the fungal elicitor into the MS medium in an amount of 10% by vo...
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