Method for identifying Vietnam camellia oleifera, Camellia odorata, Camellia frutescens and common Camellia oleifera

A technology of Camellia oleifera and Camellia oleifera is applied in the fields of Camellia oleifera, common Camellia oleifera, Fragrant Camellia oleifera, and Camellia oleifera.

CN114574614APending Publication Date: 2022-06-03海南省农业科学院热带园艺研究所
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Patent Information

Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Publication Date
2022-06-03

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Abstract

The invention relates to a method for identifying Camellia Vietnamese (Camellia Vietnamese), Camellia nobilis (C. osmantha), Camellia frutescens (i.e., Camellia oleifera, C. oleifer var.monosperma) and Camellia oleifera (i.e., Camellia oleifera, C. oleifer). The invention relates to a method for identifying Camellia vietnamese, Camellia nobilis, C. oleifer. According to the method, an amplification primer ycf1-5 and a forward sequence (5 '-3') are adopted, wherein the forward sequence is TGACCTCTTAACCAGTTTTTCCA; and the reverse sequence (5 '-3') is TGGATTATCAAGGGCATTCCGT. The detection kit is used for detecting SNP1, SNP2 and InDel 1. An amplification primer is ZDJ-190, and the forward sequence (5 '-3') of the amplification primer is AAAGAGCGTGGAGGTTCGAG; and the reverse sequence (5 '-3') is GACTGGGTGGTCGAGTCATG and is used for detecting the InDel 2 site. After the amplification product is sequenced, the SNP1 and SNP2 in the product sequence of the camellia fragrant flower germplasm material primer ycf1-5 are shown as' T 'basic groups; if the InDel 1 lacks the TCTTT sequence, the camellia meiocarpa is the camellia meiocarpa. The InDel 2 site is Vietnam camellia oleifera if the'AGTAC 'sequence is deleted, and the InDel 2 site is common camellia oleifera if the'AGTAC' sequence is not deleted. Therefore, the Vietnam camellia oleifera resources, the Camellia odorata resources, the Camellia microcarpa resources and the common Camellia oleifera resources can be effectively detected and identified, and a technical support is provided for classification identification and molecular breeding selection of related Camellia oleifera resources.
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Description

technical field

[0001] The invention belongs to the technical field of molecular biology and plant molecular breeding, and in particular relates to an identification method for Vietnamese Camellia oleifera, Fragrant Flower Camellia oleifera, Small Fruit Camellia oleifera and common Camellia oleifera. Background technique

[0002] Camellia oleifera, together with coconut, olive oil and oil palm, is also known as the world's four major woody oil crops. The unsaturated fatty acid content of tea seed oil of Camellia oleifera can reach about 90%, which is a high-grade health-care edible oil. Camellia oleifera currently has a cultivation area of ​​about 70 million mu in China. Camellia oleifera cultivated in China involves multiple species of Camellia genus, including Camellia oleifera, the main species of Camellia oleifera in the Camellia oleifera group. There are many similarities in the morphology of these four species, especially the morphological identification at the seedl...

Examples

Embodiment 1

[0033] Example 1: Molecular identification between different Camellia oleifera species germplasm resources

[0034] 1. Select experimental materials

[0035] The Camellia oleifera species from the Camellia oleifera group distributed in South China were taken. Among them, Camellia oleifera from Vietnam came from 7 populations in Hainan Province, 2 populations in Guangdong Province, and 3 populations in Guangxi Zhuang Autonomous Region. From 2 populations in Guangxi Zhuang Autonomous Region, common camellia came from 2 populations in Guangxi Zhuang Autonomous Region and 1 population in Jiangxi Province, each population sequenced 5 samples, a total of 90 samples. For SNP and Indel specific marker validation.

[0036] 2. SNP and Indel marker detection

[0037] 2.1 Using the improved CTAB method to extract the total DNA of the above experimental materials Camellia oleifera samples;

[0038] 2.2 Use the DNA of the Camellia oleifera sample to be tested extracted in step 2.1 as the...