Indole acetaldehyde dehydrogenase gene ald2 and overexpression and application

A technology of indoleacetaldehyde dehydrogenase and overexpression, applied in the field of indoleacetaldehyde dehydrogenase gene ald2 and its overexpression and application, can solve the problems of IAA biosynthesis reduction and biosynthesis redundancy

Active Publication Date: 2019-01-18
NANJING AGRICULTURAL UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, the key enzymes encoding rate-limiting steps in bacteria and plants include indole-3-pyruvate decarboxylase (IPDC) and indole-3-acetaldehyde dehydrogenase (IAAld), which are missing in bacteria and Azotobacter brasiliensis. All genes can lead to a decrease in IAA biosynthesis, but no IAA complete de

Method used

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  • Indole acetaldehyde dehydrogenase gene ald2 and overexpression and application
  • Indole acetaldehyde dehydrogenase gene ald2 and overexpression and application
  • Indole acetaldehyde dehydrogenase gene ald2 and overexpression and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0033] Embodiment 1 strain activation and preparation

[0034] 1. Observation of strains: NJAU4742 strain is Trichoderma guizhouense, which has the following characteristics: filamentous fungus, hyphae with septal arbuscular shape, conidiophores are smooth, green, the top is enlarged and spherical, and there are small growths on it. Stems produce spores, conidia are smooth spherical, green.

[0035] 2. Culture of strains

[0036] 1) Inoculate NJAU4742 into a solid medium PDA glass petri dish, culture conditions: 28°C, 7 days, wash and scrape the green spores on the petri dish with 5mL sterile water, filter with sterile gauze to sterilize A spore suspension was prepared in a glass bottle for use.

[0037] 2) Inoculate the Trichoderma harzianum NJAU4742 spore liquid into the configured PDA medium according to 1% and shake the flask for culture, the liquid volume is 20%-50% of the volume of the Erlenmeyer glass bottle, and the culture conditions are: temperature is 28°C, 180rmp...

Embodiment 2

[0038] Example 2 The growth-promoting effect of Trichoderma harzianum NJAU4742 on cucumber under hydroponic aseptic conditions

[0039] 1. Growth-promoting effect

[0040] Cucumber seeds used in this study were Lufeng cucumbers from Jiangsu Academy of Agricultural Sciences. Seeds were sterilized in 70% (v / v) ethanol for about 5 minutes, then soaked in 20% sodium hypochlorite (NaClO) for 20 minutes, and then rinsed with sterile water at least 4 times. The sterilized aseptic seeds were germinated in the dark at 30°C for 24 hours, and then the germinated seeds were placed on the beaker column containing the nutrient solution for aseptic culture for 7 days, and the aseptic seedlings with the same growth were transferred into the 50mL container containing 50mL Hoagland's nutrient solution was cultured in a triangular flask, and Trichoderma cells were inserted for interaction experiments. On the 10th day of the interaction, the results of significant growth differences among the tre...

Embodiment 3

[0045] Embodiment 3 Cucumber Root System IAA Content Determination

[0046] Cucumber roots were cut and ground in liquid nitrogen, frozen and ground, dissolved in methanol for extraction, and determined by ELISA method:

[0047] 1) Adding samples: set blank wells, standard wells, and sample wells to be tested respectively. Add 50 μl of sample diluent to the blank well, and add 50 μl of standard substance or sample to be tested in the remaining wells. Be careful not to have air bubbles. Add 50 μl of Detection Reagent A (prepared just before use) to the well, cover the microtiter plate with a membrane, and incubate at 37°C for 1 hour.

[0048] 2) Discard the liquid, shake dry, add 350 μl of 1x Wash Solution, soak for 1-2 minutes, and shake dry. Wash the plate 3 times, put the microplate upside down on absorbent paper for the last time, and blot the liquid.

[0049] 3) Add 100 μl of Detection Reagent B working solution (prepared just before use) to each well, add a membrane, a...

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Abstract

The invention discloses an indole acetaldehyde dehydrogenase gene ald2 and an overexpression method and application thereof. An IAA biosynthesis key gene ald2 of Trichoderma harzianum NJAU4742 is disclosed, and the nucleotide sequence is shown in SEQ ID NO: 1. The gene ald2 of IAA biosynthesis key gene ald2 of Trichoderma harzianum NJAU4742 is provided. A method for overexpression of an indoleacetaldehyde dehydrogenase gene ald2. The application of indole aldehyde dehydrogenase gene ald2 and its overexpressed fragment in the construction of Trichoderma harzianum NJAU4742 with significantly increased IAA production. The ald2 gene of the newly discovered Trichoderma harzianum NJAU4742 plays an important role in the IAA synthesis process, and the IAA content at the columnar sheath position inthe root hair region of the plant main root system can be significantly increased after the gene is overexpressed. The present invention provides theoretical basis and technical guarantee for the development of novel Trichoderma bio-organic fertilizer and ecological agriculture.

Description

technical field [0001] The invention belongs to the field of genetic engineering and relates to an indole acetaldehyde dehydrogenase gene ald2 and its overexpression and application. Background technique [0002] Indole-3-acetic acid, also known as auxin (IAA), is a type of plant endogenous hormone containing an indole ring structure, which can regulate the growth of plant cells, the differentiation of roots, stems and leaves, and the development of fruits. Each stage plays an important role. Studies have shown that beneficial microorganisms in the rhizosphere can also synthesize IAA, although the amount of synthesis is relatively small, and the beneficial microorganisms in the rhizosphere of the genus Trichoderma (Trichoderma spp.) have become a research hotspot. Trichoderma is an important class of plant growth-promoting bacteria, which not only has strong rhizosphere colonization ability, but also can significantly promote plant growth and development. It has been repor...

Claims

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Application Information

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IPC IPC(8): C12N9/02C12N15/53C12N1/15C12R1/885
CPCC12N1/14C12N9/0008
Inventor 沈其荣刘东阳刘秋梅黄启为李荣
Owner NANJING AGRICULTURAL UNIVERSITY
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