Gibberella gene engineering bacterium and its preparation and application

A technology of genetically engineered bacteria and Gibberella, which is applied in the field of genetic engineering, can solve the problems of time-consuming and laborious results, unclear goals, and low potential, and achieve the effects of high efficiency, clear breeding goals, and strong capabilities

Inactive Publication Date: 2005-08-17
ZHEJIANG UNIV OF TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the traditional strain breeding method mainly relies on random physical and chemical mutagenesis, the target is not clear, time-consuming and laborious, and the effect

Method used

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  • Gibberella gene engineering bacterium and its preparation and application
  • Gibberella gene engineering bacterium and its preparation and application
  • Gibberella gene engineering bacterium and its preparation and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0054] Embodiment 1: Construction of overexpression vector

[0055] step:

[0056] (1) The strong promoter Pgpd was amplified by PCR from the plasmid pAN7-1 (Punt et al.1987 Gene 56:117-124), and cloned into the vector pCB1004 (Carroll et al.1994 Fungal Genet.Newsl.41:22) to form the recombinant plasmid pCB1004Pgpd. The strong promoter Pgpd can also be derived from any other DNA containing this sequence or synthesized directly. In addition to Pgpd, promoters constitutively expressed in filamentous fungi such as PtrpC can also be used. In addition to pCB1004, plasmids used to construct cps / ks gene overexpression vectors can also be expressed in filamentous fungi, such as pCSN43, pCSN44, pCB1004, pCB1003, pSH75, pMYX100, pMSN1 and pAN26.

[0057] (2) Design primers (forward primer: GG) according to the sequence of the gibberellin synthase gene cps / ks (GeneBank accession number: AJ810802) of G. GGATCC GCCGTACGTATGAAACACACCT, the underlined sequence is the cutting site of res...

Embodiment 2

[0059] Embodiment 2: Construction of overexpression vector

[0060] step:

[0061] (1) The strong promoter PtrpC was amplified by PCR from the plasmid PZPnat1, and cloned into the corresponding site of the vector pBARKS1 by the restriction enzyme XbaI / BamHI to form the recombinant plasmid pBARtrpC.

[0062] (2) Design primers (forward primer: GG) according to the sequence of the gibberellin synthase gene cps / ks (GeneBank accession number: AJ810802) of G. GGATCC GCCGTACGTATGAAACACACCT, the underlined sequence is the cutting site of restriction enzyme BamH I; reverse primer: CC CTCGAG TACATATCAAAATTACCAGCT, the underlined sequence is the cutting point of restriction enzyme Xho I), and the sequence of the coding region was amplified by PCR technology. PCR reaction conditions: denaturation at 94°C for 5 min; followed by 32 cycles with parameters of 94°C for 1 min; 55°C for 30 sec and 72°C for 2 min; and finally extension at 72°C for 5 min.

[0063] (3) After the PCR product w...

Embodiment 3

[0064] Embodiment 3: the acquisition of engineering bacteria

[0065] step:

[0066] (1) Inoculate Gibberella fujikura onto a PDA medium plate and cultivate at 24°C for 10 days;

[0067] (2) The spores were washed with sterile water, transferred to 100 mL of YpSs liquid medium, and cultured with shaking at 24°C and 200 rpm for 36 hours;

[0068] (3) Centrifuge at 4000rpm for 5 minutes after the culture solution is filtered to obtain spore precipitation, and wash three times with sterile deionized water;

[0069] (4) Suspend the spores with 200 μl of 0.1M lithium acetate solution;

[0070] (5) Take 5 μl of the plasmid pCBcps obtained in Example 1 (concentration 2 μl / μl), add it to the spore suspension, then add spermidine to make the final concentration 4 mM, and incubate at 4° C. for 30 minutes;

[0071] (6) Add 150 μl of 0.1 M lithium acetate solution of 40% PEG8000, and continue to incubate at 4° C. for 1 hour;

[0072] (7) Heat shock in a water bath at 37°C for 5 minute...

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Abstract

The present invention provides one kind of genetically engineered bakanae fungus. The genetically engineered bakanae fungus is prepared through the process of: PCR amplification of rate-limiting enzyme gene cps/ks synthesized with gibberellin and powerful promoter Pgpd or PtrpC, cloning them to corresponding sites of the target plasmid capable of expressing in mycelial fungus to obtain super-expressing cps/ks gene vector with driving powerful promoter, transforming the super-expressing cps/ks gene vector into bakanae fungus to obtain the genetically engineered bakanae fungus. The present invention improves bakanae fungus by means of genetic engineering technology, and has determined fungus culturing target and high efficiency. The obtained engineered bakanae fungus has powerful gibberellin synthesizing ability, 40 % raised from the initial bakanae fungus strain.

Description

(1) Technical field [0001] The invention provides a gibberellin gene engineering bacterium capable of producing gibberellin and its preparation and application, belonging to the field of genetic engineering. (2) Background technology [0002] Gibberellins (Gibberellins, GAs) is a plant growth regulator, which plays a very important role in plant growth and development. It can promote the internode elongation of plants, relieve the dormancy of seeds, tubers and buds, promote flowering of plants, induce parthenocarpy and inhibit senescence, etc. Gibberellins are widely used in fruits, vegetables, rice and other crops. Gibberellins can also be used in the beer production industry. In recent years, with the promotion and use of gibberellin, the market demand has been increasing. [0003] Gibberellin is mainly produced by microbial fermentation, and the producing bacterium is the rice bakanae pathogen Gibberella fujikuroi, and gibberellin is the isoprene secondary metabolite o...

Claims

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Application Information

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IPC IPC(8): C12N1/15C12N15/09C12N15/80C12P27/00
Inventor 朱廷恒王渭霞裘娟萍
Owner ZHEJIANG UNIV OF TECH
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