CN110583654A - Plant source nematicide - Google Patents

Plant source nematicide Download PDF

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Publication number
CN110583654A
CN110583654A CN201910880623.5A CN201910880623A CN110583654A CN 110583654 A CN110583654 A CN 110583654A CN 201910880623 A CN201910880623 A CN 201910880623A CN 110583654 A CN110583654 A CN 110583654A
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CN
China
Prior art keywords
gabapentin
nematicide
plant
nematodes
root
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201910880623.5A
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Chinese (zh)
Inventor
王绍辉
赵文超
杨进山
冯加平
杨瑞
黄煌
孙露露
赵福宽
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Beijing University of Agriculture
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Beijing University of Agriculture
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Publication date
Application filed by Beijing University of Agriculture filed Critical Beijing University of Agriculture
Priority to CN201910880623.5A priority Critical patent/CN110583654A/en
Publication of CN110583654A publication Critical patent/CN110583654A/en
Pending legal-status Critical Current

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    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/44Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids

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  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

The invention relates to a botanical nematicide, which can be separated from tomato root secretion, is called Gabapentin in English and is called Gabapentin in Chinese, has extremely strong lethality to southern root-knot nematodes under the condition of water solubility, and is suitable for preventing and treating crop nematode diseases caused by pathogenic nematodes. The gabapentin is a plant source chemical substance, and experimental results show that the mortality rate of the gabapentin to second-instar larvae of the meloidogyne incognita reaches more than 90%, the effect of killing the nematodes is extremely obvious, the gabapentin has a positive effect on prevention and control of the meloidogyne incognita, and an effective management tool is provided for prevention and control of vegetable meloidogyne.

Description

Plant source nematicide
Technical Field
The invention belongs to the technical field of pesticides, and particularly relates to a botanical nematicide which has extremely strong lethality to meloidogyne incognita and is suitable for meloidogyne incognita diseases caused by meloidogyne incognita, especially tomato meloidogyne incognita.
Background
Plant parasitic nematodes are pathogenic microorganisms with great harm, are wide in distribution range, various in variety and strong in environmental adaptability, can be parasitic in tissues such as plant roots, can damage host plants through feeding activities, graze the nutrition of the host plants, particularly can cause a series of unknown pathological changes of the host plants through esophageal gland secretions, and can cause other pathogenic microorganisms to infect the host plants together, so that compound diseases are caused, and loss which is difficult to control is caused. In China, the tomato yield reduction caused by plant parasitic nematodes every year is very serious, and the development of tomatoes and other vegetables in China is greatly restricted.
The application of chemical agents is one of the most effective chemical means for preventing and treating plant pathogenic nematode diseases, but the chemical agents used in the current market can harm ecological safety and food safety, so that the demand of people on plant source chemical substances is generated, the prevention and treatment of the plant pathogenic nematode diseases by using new plant source pesticides is a good solution, and other methods such as crop layout adjustment, different pesticide rotation and the like hardly have obvious effects in the actual operation process.
Due to the concern of food safety, people tend to research high-efficiency, low-toxicity and low-residue chemical substances of plant sources.
Gabapentin, its structural formula is as follows, chemical name: 1- (aminomethyl) cyclohexaneacetic acid, a derivative of gamma-aminobutyric acid (GABA), known as Gabapentin throughout English, is soluble in water, is the first antiepileptic drug developed by Warner-Lanbert, USA, is first marketed in the United kingdom in 1993, Gabapentin is a novel antiepileptic drug,
at present, gabapentin is mainly used for preparing antiepileptic drugs, and the application of gabapentin in the field of nematocidal is not seen.
Disclosure of Invention
One of the objects of the present invention is to provide a novel use of gabapentin.
The new application of gabapentin provided by the invention is the application of gabapentin in the following 1) -3):
1) as nematicides;
2) preparing a nematicide;
3) preventing and controlling plant root-knot nematode diseases;
the nematode may specifically be a meloidogyne incognita,
the plant can be fruit vegetables such as cucumber, watermelon, melon, tomato, etc., root vegetables such as various leaf vegetables, radish, etc., tobacco, etc., and more specifically tomato.
It is another object of the present invention to provide a nematicide.
The nematicide provided by the invention takes gabapentin as an active ingredient,
in the nematicide, the gabapentin can be used as an active ingredient alone or can be combined with at least one other chemical active compound to be used as an active ingredient for killing the nematodes.
The nematicide can be prepared into various formulations, such as aqueous solution, aqueous emulsion, wettable powder, soluble granules, water dispersible granules, suspending agent, oil suspending agent, tablets or effervescent granules.
The inventor of the invention detects gabapentin from tomato root secretion, and the gabapentin is a single plant-derived chemical substance; and the experimental result shows that the mortality rate of gabapentin to the second-instar larvae of the meloidogyne incognita reaches more than 90%, the effect of killing the nematodes is extremely obvious, the active effect on preventing and controlling the meloidogyne incognita is achieved, and an effective management tool is provided for preventing and controlling the meloidogyne incognita of vegetables.
Drawings
FIG. 1 is a chromatogram of tomato root exudate.
FIG. 2 is a graph showing the statistics of mortality of second instar larvae of Meloidogyne incognita under the effect of gabapentin at different concentrations.
Detailed Description
The present invention will be described below with reference to specific examples, but the present invention is not limited thereto.
The experimental methods used in the following examples are all conventional methods unless otherwise specified; reagents, materials and the like used in the following examples are commercially available unless otherwise specified.
Example 1 detection of gabapentin from tomato root-line secretions
Method of producing a composite material
1.1 sample Pre-treatment
Collecting tomato root secretion by root soaking method, and referring to methods (2010) of Zhou Bao Li et al, slightly modifying. When the tomato plants grow to 5 weeks old and are four-leaf and one-heart, a root secretion collecting test is carried out, and 6 plants are inoculated in each treatment. The tomato roots were cleaned with distilled water, placed in a beaker covered with tinfoil paper, and the appropriate amount of water (about 30ml of water per plant root) was added and aerated for cultivation. Changing water every 4h, collecting for 3 times, mixing, filtering, and concentrating the collected secretion. Collecting concentrated secretion before 1ml, adding 3 times volume of methanol, mixing by vortex shaking for 1min-3min, standing at 4 deg.C for 10min, centrifuging at 13000rpm for 10min, collecting supernatant, and vacuum drying. Redissolving 100ul of methanol for testing.
1.2 chromatographic methods
A chromatographic column: agilent ZORBAX Eclipse Plus C18, 2.1X100mm,3.5 um.
Column temperature 35 ℃, sample introduction 3ul, flow rate 0.5mL/min, mobile phase A: H2O (0.1% Formic Acid), mobile phase B: Acetonitrile (0.1% Formic Acid), gradient elution conditions:
1.3 Mass Spectrometry method
Electrospray ionization (ESI) source, positive and negative ion ionization mode. The ion Source temperature (Source temperature) is 120 ℃, the desolvation temperature (desolvation temperature) is 500 ℃, the desolvation nitrogen flow is 600L/h, and the cone hole back flushing nitrogen (con gas flow) is 50L/h. The ionization voltage of the capillary in the positive and negative ion modes is 3.0kV and 4.5kV respectively, the sampling taper hole voltage (sampling cone) is 27eV, the extraction taper hole (extraction cone) is 4eV, and the scanning range of a quadrupole rod is m/z 50-1500.
TABLE 1 detection of gabapentin information in root exudates
In the above tables, sample-1, sample-2, sample-3 and sample-4 refer to parallel experiments
FIG. 1 is a chromatogram of tomato root exudate.
As can be seen from table 1 and fig. 1: gabapentin was detected in tomato root secretions, thus demonstrating that gabapentin is a single chemical of plant origin.
Example 2 detection of nematicidal Activity of gabapentin
(1) Weighing 172g of solid gabapentin, dissolving in 1L of pure water to prepare a mother solution with the concentration of 1 mol/L;
(2) diluting the prepared mother liquor into working solution of 1mmol/L and 0.1mmol/L in proportion for later use;
(3) placing the pre-hatched second-instar larvae of meloidogyne incognita in a 12-well cell culture plate, wherein each well has about 50 second-instar larvae;
(4) immersing a cell culture plate in which the second-instar larvae of the meloidogyne incognita are placed in the prepared working solution, and observing the nematodes after 24 hours;
(5) the calculation formula of the mortality rate is as follows: mortality rate is 100% of the number of nematodes/total number of nematodes.
FIG. 2 is a graph showing the statistics of mortality of second instar larvae of Meloidogyne incognita under the effect of gabapentin at different concentrations.
From fig. 2 it can be found that: under the condition of comparison with clear water, the lethality of the two concentrations to the second-instar larvae reaches over 90 percent, and the effect is extremely obvious, so that the gabapentin has positive effect on the prevention and treatment of the root-knot nematodes.

Claims (7)

1. The use of gabapentin in 1) -3) as follows:
1) as nematicides;
2) preparing a nematicide;
2) preventing and controlling plant root-knot nematode diseases.
2. Use according to claim 1, characterized in that: the nematode is Meloidogyne incognita.
3. Use according to claim 1 or 2, characterized in that: the plant is fruit vegetable, leaf vegetable, root vegetable or tobacco.
4. Use according to claim 3, characterized in that: the plant is tomato.
5. A nematicide contains gabapentin as an active ingredient.
6. The nematicide of claim 5, wherein: the nematicide also contains at least one chemically active compound.
7. The nematicide of claim 5 or 6, wherein: the nematicide can be prepared into various formulations, including aqueous solution, aqueous emulsion, wettable powder, soluble granules, water dispersible granules, suspending agent, oil suspending agent, tablets and effervescent granules.
CN201910880623.5A 2019-09-18 2019-09-18 Plant source nematicide Pending CN110583654A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910880623.5A CN110583654A (en) 2019-09-18 2019-09-18 Plant source nematicide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910880623.5A CN110583654A (en) 2019-09-18 2019-09-18 Plant source nematicide

Publications (1)

Publication Number Publication Date
CN110583654A true CN110583654A (en) 2019-12-20

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Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1449750A (en) * 2003-05-12 2003-10-22 徐州恩华药业集团有限责任公司 Gabapentin slow -released composition
CN1720025A (en) * 2002-10-08 2006-01-11 兰贝克赛实验室有限公司 Gabapentin tablets and methods for their preparation
CN1832736A (en) * 2003-08-05 2006-09-13 兰贝克赛实验室有限公司 Stable sustained release oral dosage form of gabapentin
CN102690207A (en) * 2012-05-31 2012-09-26 湖北楚阳科技股份有限公司 Gabapentin synthesizing method
CN104496833A (en) * 2014-11-26 2015-04-08 太仓运通生物化工有限公司 Gabapentin synthesis technology
CN105061239A (en) * 2015-08-18 2015-11-18 太仓运通生物化工有限公司 Gabapentin synthesis method
CN105949042A (en) * 2016-06-07 2016-09-21 王昌荣 Gabapentin pharmaceutical composition and medical application thereof

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1720025A (en) * 2002-10-08 2006-01-11 兰贝克赛实验室有限公司 Gabapentin tablets and methods for their preparation
CN1449750A (en) * 2003-05-12 2003-10-22 徐州恩华药业集团有限责任公司 Gabapentin slow -released composition
CN1832736A (en) * 2003-08-05 2006-09-13 兰贝克赛实验室有限公司 Stable sustained release oral dosage form of gabapentin
CN102690207A (en) * 2012-05-31 2012-09-26 湖北楚阳科技股份有限公司 Gabapentin synthesizing method
CN104496833A (en) * 2014-11-26 2015-04-08 太仓运通生物化工有限公司 Gabapentin synthesis technology
CN105061239A (en) * 2015-08-18 2015-11-18 太仓运通生物化工有限公司 Gabapentin synthesis method
CN105949042A (en) * 2016-06-07 2016-09-21 王昌荣 Gabapentin pharmaceutical composition and medical application thereof

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
化工百科: "加巴喷丁", 《化工百科》 *
张志勇等: "《蔬菜病虫害防治》", 31 January 2016, 中央广播电视大学出版社 *
陆家云等: "《植物病害诊断》", 30 September 1997, 中国农业出版社 *

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Application publication date: 20191220