Delta 8 desaturase new gene derived from pavlova viridis

A desaturase and gene technology, applied in the field of desaturase genes and their separation, can solve the problems of different enzyme activities and functions, differences in sequence structure, etc.
CN104293769AInactive Publication Date: 2015-01-21青岛东方商旅置业有限公司

Patent Information

Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
青岛东方商旅置业有限公司
Publication Date
2015-01-21
Estimated Expiration
Not applicable · inactive patent

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Abstract

The invention discloses delta 8 desaturase new gene derived from pavlova viridis. Polyunsaturated fatty acids, such as timnodonic acid EPA and docosahexaenoic acid DHA, are important nutrient substances which are necessary for a human body and cannot be synthesized by the human body per se. Aiming at microalgae, namely, pavlova viridis, which can synthesize EPA and DHA naturally, the application adopts conservative district sequence amplification combined with RACE to clone so as to obtain a new delta 8 fatty acid desaturase gene. Due to the obtaining of the gene, basis is provided for further knowing and utilizing an EPA and DHA biosynthesis process which has extremely great practical significance.
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Description

technical field

[0001] The application belongs to the technical field of gene cloning and separation, and in particular relates to a desaturase gene related to the synthesis of polyunsaturated fatty acids derived from microalgae and its separation method. Background technique

[0002] Polyunsaturated fatty acids are essential nutrients for the human body, and microalgae are an important biological resource because they are rich in polyunsaturated fatty acids. Pavlova viridis is rich in EPA (eicosapentaenoic acid) and DHA (docosahexaenoic acid), and is a good experimental material for identifying and cloning polyunsaturated fatty acid-related synthesis genes.

[0003] The full name of RACE is rapid-amplification of cDNA ends, which is a commonly used technology for rapid cloning of cDNA ends by PCR. In this experiment, RACE technology was used to obtain the full-length sequence of the target mRNA fragment.

[0004] In the biosynthetic pathway of EPA and DHA in microalgae, ...

Claims

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