Aspergillus versicolor strain with antibacterial activity
A technology of Aspergillus versicolor and antibacterial activity, which is applied in the field of Aspergillus versicolor, can solve the problems of separation of antibacterial active substances, repeated discovery of increased natural antibacterial active products, etc., and achieve good development and application value and strong inhibitory effect
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specific Embodiment approach 1
[0013] Specific embodiment one: the Aspergillus versicolor with bacteriostatic activity in this embodiment is Aspergillus versicolor (Aspergillus versicolor) CWJ2, preserved in China Center for Typical Culture Collection (CCTCC), preservation address is Wuhan University, Wuhan City, preservation date is April 2014 On March 16, the deposit number is CCTCC NO: M2014130.
[0014] After the present embodiment Aspergillus versicolor CWJ2 is cultivated on PDA solid medium for 5 days, texture is velvety; Tool a large amount of conidia structure, green, edge white (such as figure 1 ); no exudate; mild musty smell; the opposite side of the colony is yellowish to orange in varying degrees. The top of the conidiophores of Aspergillus versicolor CWJ2 swelled into an apical capsule, which was spherical (such as figure 2 ). The surface of the top capsule is covered with radial stalks.
[0015] In this embodiment, Aspergillus versicolor CWJ2 can grow on PDA medium, and the optimum growth...
specific Embodiment approach 2
[0016] Specific embodiment 2: In this embodiment, Aspergillus versicolor CWJ2 is screened from healthy Acanthopanax plants in Maoershan area, Heilongjiang Province, China. Screening is carried out according to the following steps: select healthy Acanthopanax roots, rinse them with tap water, blot dry with sterile filter paper, cut them into 1cm segments, and carry out surface disinfection according to the following aseptic procedures: alcohol with a volume concentration of 75% Rinse for 1 min—10% hydrogen peroxide rinse for 15 min—75% alcohol rinse for 1 min—sterile water rinse for 3 times. Place the sterilized experimental material in PDA solid medium, and culture it in a constant temperature incubator at 28°C for 10 to 15 days. After mycelium grows around the experimental material, pick the mycelium and transfer it to a plate (PDA solid medium) Separation and purification were performed by streaking multiple times, and the purified strain was placed in a slant medium (PDA so...
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