Chip for screening phytoplasma in 16SrXII group and application thereof
A plant-based, chip technology, applied in the field of bioinformatics and bio-quarantine identification, can solve problems such as cross-contamination, low sensitivity, lack of versatility and standardization, achieve good stability, improve customs clearance rate, and visualize analysis results Effect
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Embodiment 1
[0060] Example 1. Preparation of a chip for screening 16SrXII group phytoplasma
[0061] 1. Design of group-level highly compatible oligonucleotide probes
[0062] 1) Download the 16SrXII group phytoplasma genome and nucleic acid sequence data from the National Center for Biotechnology Information (NCBI) and the official website of the Ribosome Database Project (RDP) database to design probes.
[0063] 2) Organize phytoplasma nucleic acid sequences, remove nucleic acid sequences less than 200 bp in length and group them; all phytoplasma sequences in the same group are referred to as in-group sequences, and all phytoplasma sequences not in this group are referred to as out-group sequences.
[0064] 3) Use Cluster W to align the sequences in the group, find the sequence conserved regions and design probes. When designing the probe, use 2 to 3 bases as the interval in the conserved region of the sequence, continuously extract all 19 bp nucleic acid sequences, and screen the sele...
Embodiment 2
[0075] Example 2, the application of the chip for screening 16SrXII group phytoplasma
[0076] 1. Chip detection samples for screening 16SrXII group phytoplasma
[0077] 1. Extraction of total DNA from samples used for detection
[0078] 1) Get the grape leaves infected with Australian phytoplasma candidate species (the leaves show red flowers and curls, and the Latin name of phytoplasma: candidatus phytoplasma australiense, recorded in: Candidatus Phytoplasma australiense is the phytoplasma associated with Australian grapevine yellows, papaya dieback and Phormium yellow leaf diseases, 1998, 104: 619-623. The public can obtain from the Chinese Academy of Inspection and Quarantine.) 0.1g, take an appropriate amount of liquid nitrogen to grind, and then add the grinding liquid (K 2 HPO 4 .3H 2 O 2.17g, KH 2 PO 4 0.41g, sucrose 10g, BSA (Fraction V) 0.15g, PVP-102g to 100mL, adjust the DH to 7.6, high temperature sterilization) 2mL fully grind, centrifuge at 20000rpm at 4°C ...
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