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Aenasius bambawalei glucose dehydrogenase GLD gene and primer combination and cloning method for amplification of aenasius bambawalei glucose dehydrogenase GLD gene

A technology of glucose dehydrogenase and Bencroft's jumping bee, which is applied in the fields of botany equipment and methods, biochemical equipment and methods, genetic engineering, etc., and can solve the problems of no sequence upload record, literature report, etc.

Active Publication Date: 2019-12-20
ZHEJIANG ACADEMY OF AGRICULTURE SCIENCES
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0004] At present, there is no relevant research report on the GLD gene of Leaperia bancroft. The sequences of GLD genes of other parasitoids in the NCBI database are also predicted sequences, and there are no accurate sequence upload records and related literature reports.

Method used

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  • Aenasius bambawalei glucose dehydrogenase GLD gene and primer combination and cloning method for amplification of aenasius bambawalei glucose dehydrogenase GLD gene

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Effect test

Embodiment 1

[0042] (1) Extraction of Genomic DNA of Leaperia bancroft

[0043] Genomic DNA was extracted from 5 whole female adults of L. bancroftensis. The extraction method was carried out according to the instructions of the Genomic DNA Kit kit from TIANamp Company.

[0044] (2) Design of primers for the CDS region sequence of the GLD gene of Leaperia bancroft

[0045] According to the existing GLD gene transcriptome data of Leaperia bancrofti in our laboratory, and referring to the predicted GLD gene sequence of Leaperia bancrofti similar to the pupae of the fly pupae (GenBank accession number: XM_016982053), the Prediction of the CDS region of the GLD gene of A. japonica, and design of primers for the predicted sequence, the designed primer sequence is as follows: Design an upstream amplification primer (A-Gld-p1F: ctcgcagtacactcgcaaac) within 130 bp before the start codon (sequence is as follows) , and a downstream primer (A-Gld-p2R: aacaggttggagtgcgagag) was designed on the exon a...

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Abstract

The invention provides an aenasius bambawalei glucose dehydrogenase GLD gene and a primer combination and cloning method for amplification of the aenasius bambawalei glucose dehydrogenase GLD gene, and belongs to the technical field of molecular biology and gene cloning. The nucleotide sequence of the GLD gene is shown as SEQID No.6. The gene is obtained, so that composition and gene structure ofthe gene in cells of aenasius bambawalei can be further studied, and a theory basis is provided for effects of the gene in reproductive physiology of the aenasius bambawalei, the position of the functional area, and differentiation from other species.

Description

technical field [0001] The invention relates to the technical fields of molecular biology and gene cloning, in particular to the glucose dehydrogenase GLD gene of Leapers bancroft and its amplification primer combination and cloning method. Background technique [0002] Glucose dehydrogenase (GLD) is a class of small peptide molecules with diverse structures and functions, with a molecular weight of about 2Kbp and an isoelectric point between 5 and 7. The gene is widely distributed in arthropods. In egg and larval stages, the gene is distributed in many epidermis-derived tissues of insects, including some reproductive organs of the body wall; however, in the adult stage, the gene is only conserved in some reproductive organs. In organs such as spermatheca. For parasitoid females, the number of sperm absorbed and released is closely related to the number of fertilized eggs. The GLD gene can improve the fertilization ability of females by affecting the storage and release of...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12N15/53C12N9/04C12N15/11C12N15/10
CPCC12N9/0006C12Y101/9901C12Q1/686C12Q2521/101
Inventor 张娟黄俊吕要斌唐娅媛李明江
Owner ZHEJIANG ACADEMY OF AGRICULTURE SCIENCES
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