Bacterium for inhibiting growth of Gambierdiscus sp. and application thereof
A technology of algal growth and sub-algae, applied in the application, bacteria, plant growth regulators and other directions, can solve the problems of difficult treatment, difficult metabolic clearance and other problems, and achieve the effect of reducing the secretion of ciguatoxin
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Embodiment 1
[0065] Embodiment 1, isolation and identification of bacterial strain XZX-S5
[0066] 1. Isolation, cultivation and screening of algae cell symbiotic bacteria
[0067] Aseptically take out Gambierdiscus sp.1112M1M03, shake it and let it stand for a while (3-5 minutes), take the supernatant and dilute it in multiples, and spread it on a clean bench to obtain cultureable bacterial single clones. After the selected monoclonal strains were cultured, they were co-cultured with Gambierdiscus sp.1112M1M03. After cultivation, the number of algal cells, chlorophyll content and photosynthetic efficiency were detected, and the strains that inhibited the growth of Gambierdiscus were marked as potential inhibitors. Algae strains, and select the algae-inhibiting strain with the most obvious inhibitory effect, and name it XZX-S5.
[0068] 2. Identification of XZX-S5 strain
[0069] 1. Morphological identification
[0070] Describe the single colony state of the XZX-S5 strain isolated in t...
Embodiment 2
[0080] Embodiment 2, gamma proteobacterium Gamma proteobacterium XZX-S5 inhibits the growth of algae gambiae
[0081] 1. Preparation of experimental materials and experimental methods
[0082] 1. Preparation of experimental materials
[0083] The present invention selects Gambierdiscus sp.1112M1M03, which produces strong ciguatera toxin, as an experimental object, and studies the inhibitory effect of Gamma proteobacterium XZX-S5 on the growth of Gambierdiscus.
[0084] (1) Cultivation of Gambierdiscus sp.1112M1M03
[0085] Use a micropipette to draw 10 μL of Gambierdiscus sp.1112M1M03 algae liquid onto a glass slide, and observe the individual conditions of Gambierdiscus sp.1112M1M03 under a 40X optical microscope. After confirming that the growth state is good, transfer 20ml of Gambiae algae liquid to 100mL of fresh K medium medium for expansion. Algal cell concentrations were counted every two days. The counting method is as follows: Gently shake the Erlenmeyer flask of ...
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