CN108142443A - A kind of Herba Asari extract and its application as Genes For Plant Tolerance fungus - Google Patents

A kind of Herba Asari extract and its application as Genes For Plant Tolerance fungus Download PDF

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Publication number
CN108142443A
CN108142443A CN201711325207.6A CN201711325207A CN108142443A CN 108142443 A CN108142443 A CN 108142443A CN 201711325207 A CN201711325207 A CN 201711325207A CN 108142443 A CN108142443 A CN 108142443A
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extract
concentration
alcohol
carbendazim
herba asari
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CN108142443B (en
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王俊丽
王忠跃
刘名飞
肖泽丰
黄婧婧
刘杰
郝娜
黄航君
马伟伟
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Institute of Plant Protection of Chinese Academy of Agricultural Sciences
Minzu University of China
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Institute of Plant Protection of Chinese Academy of Agricultural Sciences
Minzu University of China
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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
    • A01N65/00Biocides, pest repellants or attractants, or plant growth regulators containing material from algae, lichens, bryophyta, multi-cellular fungi or plants, or extracts thereof
    • 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
    • A01N65/00Biocides, pest repellants or attractants, or plant growth regulators containing material from algae, lichens, bryophyta, multi-cellular fungi or plants, or extracts thereof
    • A01N65/08Magnoliopsida [dicotyledons]

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  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Plant Pathology (AREA)
  • Biotechnology (AREA)
  • Microbiology (AREA)
  • Mycology (AREA)
  • Agronomy & Crop Science (AREA)
  • Dentistry (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Natural Medicines & Medicinal Plants (AREA)
  • Medicines Containing Plant Substances (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

The present invention relates to a kind of Herba Asari extract, the Herba Asari extract is water extract or alcohol extract, and wherein alcohol extract extracting method is:It is to weigh to crush sample 800g, impregnates plant drymeal with the ethyl alcohol of 5 times of amounts, stand 12h at room temperature;Ultrasonic extraction 2h;Decompression filters, and continuous to extract 3 times, merging filtrate is concentrated at 45 DEG C with Rotary Evaporators, after dry, preserved in 4 DEG C, is spare;Application of the Herba Asari extract as Genes For Plant Tolerance fungus is further included, can significantly inhibit the generation of Aspergillus carbonerius ochratoxin A (OTA) including it.Herba Asari extract used in the present invention is a kind of botanical biological pesticide, has the characteristics that antibacterial activity is high, antimicrobial spectrum is wide, is not easy to produce resistance, is nontoxic to humans and animals, can improve grape fruit foodsafety.

Description

A kind of Herba Asari extract and its application as Genes For Plant Tolerance fungus
Technical field
The present invention relates to field of biological pesticide, and in particular to botanical biological pesticide is more particularly to a kind of asarum extraction Object and its application as Genes For Plant Tolerance fungus.
Background technology
Grape is one of most ancient, the most wide fruit of distribution in the world.Its cultivation history is of long standing and well established, and yield accounts for about generation The a quarter of boundary's fruit total output.The whole world is distributed it has been reported that more than 70 kinds vitis spps, grape variety more than 8000 are planted In temperate zone and subtropical zone, generally 20 ° -52 ° of north latitude, 30 ° -45 ° of south latitude.According to geographic origin difference, grape be divided into North America, Eurasian and three, East Asia population.China is one of vitis spp resource distribution country the abundantest, known kind of East Asia population Class has 42 kinds of China to have, also 1 subspecies, 12 mutation.The grape variety of plantation is there are about 500 kinds, grape -growing areas The whole world second is occupied, is only second to Spain.2016, China's grape area more than 800,000 hectares (12,400,000 mu), ate Portugal raw Grape yield is sure to occupy first place in the world always from after 2000.
Since grape shape flavor is all good and full of nutrition, and cultivating grape obtains good economic benefit in the past 20 years And social benefit, China's grape industry development are rapid.But grape is as other garden crops, the serious harm of pest and disease damage It is the restriction factor that industry develops in a healthy way, common, harm serious grape disease such as grape grey mould, white rot, anthracnose Deng;Causing harm for these diseases seriously affects grape quality and yield, the difficulty that must still do not solved in the production of China's grape, and And it is also problem in the production of worldwide grape.In addition, mycotoxin is to influence food security key factor, most important one There is Ochratoxin A (OTA) toxin that Aspergillus carbonerius germ generates;The content of toxins is exceeded to cause human body very big wound It is harmful or even carcinogenic.In agricultural production, it is using chemical pesticide to commonly use preventing control method, but chemical prevention exists and causes grape sick The drug resistance of opportunistic pathogen, again residual contamination, rampant equivalent risk.Therefore the vital task that non-chemical pesticide is industry development is found, It is the important topic of scientific research.Plant source method is excavated from plant, including exploitation botanical pesticide, from phytochemical The direct utilization of middle searching lead compound, even plant leaching liquor immersion is the important content of this developing direction.
Asarum (Asarum sieboldii Miq.) is Aristolochiaceae (Aristolochiaceae) asarum (Asarum) Plant originates in Shandong, Anhui, Zhejiang, Jiangxi, Henan, Hubei, Shaanxi, Sichuan, is born in dark and damp under height above sea level 1200-2100 Milins In peat.Japan and Korea also have.This kind of all herbal medicine.But it has no and is applied to preventing and treating grapevine diseases as biological pesticide Report and research.
Invention content
A kind of application the invention mainly solves the technical problem of providing Herba Asari extract and its as Genes For Plant Tolerance fungus, Comparatively ideal control effect can be reached, and there is significant inhibiting effect to Aspergillus carbonerius production OTA abilities, grape food can be improved Product safety.
In order to solve the above technical problems, the technical solution adopted by the present invention is:
A kind of Herba Asari extract, the Herba Asari extract be water extract or alcohol extract, the water extract extracting method For:It weighs asarum and crushes dry product 100g, add distilled water 1000mL, impregnate 30min.First boil with high heat, after use slow boiling instead, decoct 40min is extracted, liquid is filtered while hot with 4 layers of gauze, repeats to extract once, is concentrated into after 2 filtrates of merging with slow boiling a concentration of 1000mg/mL, 4 DEG C preserve, are spare;The alcohol extract extracting method is:It is to weigh to crush sample 800g, with the second of 5 times of amounts Alcohol impregnates plant drymeal, stands 12h at room temperature;Ultrasonic extraction 2h;Decompression filters, continuous to extract 3 times, merging filtrate, at 45 DEG C It is lower to be concentrated with Rotary Evaporators, after dry, preserved in 4 DEG C, is spare.
A kind of application of Herba Asari extract as Genes For Plant Tolerance fungus is further related to, the Herba Asari extract is to following disease disease Opportunistic pathogen has significant bacteriostatic activity, mainly including Botrytis cinerea, fruit white rot of grape bacterium, grape anthracnose and Aspergillus carbonerius Germ.
Further, wherein the grape anthracnose is included to carbendazim highly resistance anthrax bacteria bacterial strain, the grey mold Germ is included to carbendazim highly resistance ash arrhizus bacteria bacterial strain.
Further, a concentration of 6.25mg/mL-100mg/mL of the water extract, the alcohol extract are a concentration of 0.3125mg/mL-5mg/mL。
Further, when water extract is 100mg/mL, the bacteriostasis rate to anthrax bacteria, white rot germ and ash arrhizus bacteria is 40.40%th, 74.87% and 37.50%;It is 97.13% to ash arrhizus bacteria bacteriostasis rate as a concentration of 5mg/mL of alcohol extract, it is right White rot germ, anthrax bacteria, Aspergillus carbonerius germ inhibiting rate are up to 100%.As a concentration of 2.5mg/mL of alcohol extract, to 4 The bacteriostasis rate of kind pathogen is more than 85.5%;As a concentration of 5mg/mL of alcohol extract, to carbendazim sensitivity anthrax bacteria bacterium Strain FJZZ-62, coll-9, coll-20 bacteriostasis rate is respectively 96.30%, 94.33% and 96.88%, to carbendazim highly resistance anthrax Germ bacterial strain FJND-9, GZSD-89 inhibiting rate are up to 100%, also reach 96.09% to the inhibiting rate of FJND-40, to more bacterium Sensitive sense ash arrhizus bacteria bacterial strain GXGL-7, GXNN-7 germ bacterium bacteriostasis rate is up to 100%, is to GXNN-6 bacteriostasis rates 96.21%, 100% is up to carbendazim highly resistance ash arrhizus bacteria bacterial strain HBLF-10, GXZY-7 inhibiting rate, the suppression to GXZY-4 Rate processed is up to 97.01%.
Further, the alcohol extract generates OTA to Aspergillus carbonerius germ and significantly inhibits, when alcohol extract is dense When spending for 5mg/mL, it is most apparent that OTA generates lag
The beneficial effects of the invention are as follows:Herba Asari extract of the present invention is a kind of as the germ killing drugs of active ingredient Botanical biological pesticide belongs to one kind of bio-pharmaceutical, meets requirement of the modern society to novel pesticide.Secondly, Herba Asari extract Have the characteristics that antibacterial activity is high, antimicrobial spectrum is wide, be not easy to produce resistance, be nontoxic to humans and animals.In addition, it is not only to grape fruit Real encountered pathogenic bacteria has inhibition, also has significant inhibiting effect to Aspergillus carbonerius production OTA abilities, can improve grape fruit Real foodsafety.
Specific embodiment
It is described in detail with reference to preferred embodiment, so that advantages and features of the invention can be easier to by this field Technical staff's understanding, so as to make a clearer definition of the protection scope of the present invention.
Embodiment 1:
First, the preparation of water extract and alcohol extract
The asarum of the present invention is purchased from Hui nationality's medicinal material market.Lay-by material is dried, is crushed, is placed at aeration-drying and protects It deposits spare.
Water extract extracting method is:It weighs black nightshade and crushes dry product 100g, add distilled water 1000mL, impregnate 30min.First use force Fire boils, after use slow boiling instead, decoct extraction 40min.Liquid is filtered while hot with 4 layers of gauze.Repeat to extract primary, 2 filters of merging After liquid a concentration of 1000mg/mL is concentrated into slow boiling.4 DEG C preserve, are spare.Asarum alcohol extracting step is:It is to weigh crushing sample 800g impregnates plant drymeal with the ethyl alcohol of 5 times of amounts, stands 12h at room temperature;Ultrasonic extraction 2h;Decompression filters, continuous to extract 3 times, Merging filtrate is concentrated at 45 DEG C with Rotary Evaporators, after dry, preserved in 4 DEG C, is spare.
2nd, the detection method of micro-organisms and OTA
Asarum water extract, alcohol extract are measured to Botrytis cinerea (Botrytis using mycelial growth rate method Cinerea), fruit white rot of grape bacterium (Coniothyrium diplodiella), grape anthracnose (Glomerella ) and the bacteriostatic activity of Aspergillus carbonerius (Aspergillus carbonarius) cingulata.It is as follows:
After actication of culture, vigorous place is grown in culture dish edge mycelia with aseptic card punch (Ф=5mm) and uniformly punched, Bacteria cake is made, is inoculated on culture medium, each culture dish center connects a bacteria cake, temperature is 25-28 DEG C, humidity is 73% After culture 2-7d is inverted in incubator, colony diameter is surveyed with crossing method, calculates inhibiting rate.Each processing sets 3 repetitions.
Strain cultivates 14d on CYA culture mediums, plays the training for taking 12 pieces of carriers with aseptic card punch (Φ=5mm) daily Support object.The culture that will carry disease germs is put in 5mL small test tubes, and methanol 2mL, whirlpool concussion 1min, static extraction 60min are added in after weighing Afterwards, it first, then with 0.22 μm of membrane filtration, is finally examined with 0.45 μm of membrane filtration with ultra high efficiency liquid phase-cascade mass spectrometer It surveys.
Ultra high efficiency liquid phase-string mass spectrograph testing conditions:Using the superelevation liquid chromatograph XevoTM TQ-S of U.S. Water It is programmed simultaneously automatic sampling.Mobile phase is A1:Chromatography acetonitrile;A2:Chromatography methanol;B1:0.2% formic acid water;B2:Water;Flow velocity It is set as:0.3mL/min;Sample size:1μL.Every gram is calculated according to the quality of taken agar block and the content of toxins detected Toxin concentration in culture is expressed as Output of toxin (ng/g).
3rd, the bacteriostasis of water extract and alcohol extract
The result shows that asarum water extract is 74.87% to the bacteriostasis rate of white rot bacterium, fungistatic effect better than anthrax bacteria, Ash arrhizus bacteria, and there is no inhibiting effect to Aspergillus carbonerius germ.
Asarum alcohol extract shows preferable fungistatic effect to 4 kinds of grape disease fungus.When asarum alcohol extract is a concentration of It is 97.13% to ash arrhizus bacteria bacteriostasis rate during 5mg/mL, it is high to white rot bacterium, anthrax bacteria, Aspergillus carbonerius germ inhibiting rate Up to 100%.As a concentration of 2.5mg/mL of alcohol extract, to the bacteriostasis rates of 4 kinds of pathogens more than 85.5%, EC50 values are 0.48-1.10mg/mL.The fungistatic effect of asarum alcohol extract dialogue maize ear rot bacterium is best, as a concentration of 1.25mg/mL of alcohol extract, 98.08% is up to the inhibiting rate of white rot bacterium.
4th, alcohol extract is to the inhibiting effect of carbendazim sensitivity anthrax bacteria bacterial strain
As a concentration of 5mg/mL of asarum alcohol extract, to carbendazim sensitivity anthrax bacteria bacterial strain FJZZ-62, coll-9, Coll-20 bacteriostasis rates are respectively 96.30%, 94.33% and 96.88%, EC50 are respectively 0.52,0.92 and 0.46mg/mL.
5th, alcohol extract is to the inhibiting effect of carbendazim highly resistance anthrax bacteria bacterial strain
Asarum alcohol extract goes out good inhibiting effect to carbendazim highly resistance anthrax bacteria strains expressed.When alcohol extract is a concentration of During 5mg/mL, 100% is up to carbendazim highly resistance anthrax bacteria bacterial strain FJND-9, GZSD-89 inhibiting rate, to FJND-40's Inhibiting rate also reaches 96.09%.EC50 is respectively 0.46,1.39 and 0.77mg/mL.And 100 μ g/mL carbendazim to FJND-9, The inhibiting rate of FJND-40 and GZSD-89 bacterial strains is respectively 9.80%, 21.50% and 10.01%.When alcohol extract is a concentration of During 0.625mg/mL, to the inhibitory activity of the highly resistance bacterial strain also obvious activity for being better than 100 μ g/mL carbendazim.
6th, alcohol extract is to the inhibiting effect of carbendazim sensitivity ash arrhizus bacteria bacterial strain
During a concentration of 5mg/mL of asarum alcohol extract, to carbendazim sensitivity ash arrhizus bacteria bacterial strain GXGL-7, GXNN-7 germ bacterium It is 1.06-1.59mg/mL's that bacteriostasis rate up to 100%, which is 96.21%, EC50 to GXNN-6 bacteriostasis rates,.
7th, alcohol extract is to the inhibiting effect of carbendazim highly resistance ash arrhizus bacteria bacterial strain
A concentration of 100 μ g/mL carbendazim is respectively to the inhibiting rate of HBLF-10, GXZY-4 and GXZY-7 bacterial strain 53.45%th, 55.11% and 14.76%.Asarum alcohol extract has carbendazim highly resistance ash arrhizus bacteria bacterial strain preferable inhibition to make With effect is better than 100 μ g/mL carbendazim.As its a concentration of 5mg/mL, to carbendazim highly resistance ash arrhizus bacteria bacterial strain HBLF- 10th, GXZY-7 inhibiting rates are up to 100%, to the inhibiting rate of GXZY-4 up to 97.01%.Its EC50 is 1.04-1.34mg/mL.
8th, alcohol extract is to the inhibiting effect of Aspergillus Niger toxin
In blank control, OTA starts to generate in 3d, and a concentration of 6.22ng/g, 9d OTA yield peaks, dense It spends for 2970.78ng/g.After culture medium adds asarum alcohol extract, there is retardation compared with blank control in the generation of OTA.Kakuol Extract concentration is higher, and the time that OTA is generated more lags, and toxin producing is fewer.During a concentration of 0.3125mg/mL of alcohol extract, 5d is then Begin with OTA generations, a concentration of 196.44ng/g of OTA.During a concentration of 5mg/mL of alcohol extract, OTA yield lags most apparent, 9d Just there is a small amount of OTA to generate, when OTA a concentration of 31.56ng/g, 14d is 563.78ng/g, hence it is evident that less than control.
The foregoing is merely the embodiment of the present invention, are not intended to limit the scope of the invention, every to utilize this hair The equivalent structure or equivalent flow shift that bright description is made directly or indirectly is used in other relevant technology necks Domain is included within the scope of the present invention.

Claims (6)

1. a kind of Herba Asari extract, it is characterised in that:The Herba Asari extract be water extract or alcohol extract, the water extract Extracting method is:Weigh asarum and crush dry product 100g, add distilled water 1000mL, impregnate 30min, first boil with high heat, after use instead Slow boiling decocts extraction 40min, and liquid is filtered while hot with 4 layers of gauze, repeats to extract once, be concentrated after merging 2 filtrates with slow boiling To a concentration of 1000mg/mL, 4 DEG C preserve, are spare;The alcohol extract extracting method is:It weighs and crushes sample 800g, with 5 times The ethyl alcohol of amount impregnates plant drymeal, stands 12h at room temperature;Ultrasonic extraction 2h;Decompression filters, continuous to extract 3 times, merging filtrate, It is concentrated at 45 DEG C with Rotary Evaporators, after dry, preserved in 4 DEG C, is spare.
2. application of a kind of Herba Asari extract as described in claim 1 as Genes For Plant Tolerance fungus, which is characterized in that described is thin Pungent extract has significant bacteriostatic activity to following disease pathogen, mainly including Botrytis cinerea, fruit white rot of grape bacterium, Portugal Grape anthrax bacteria and Aspergillus carbonerius germ.
3. application as claimed in claim 2, which is characterized in that the wherein described grape anthracnose is included to carbendazim highly resistance Anthrax bacteria bacterial strain, the ash arrhizus bacteria are included to carbendazim highly resistance ash arrhizus bacteria bacterial strain.
4. application as claimed in claim 2 or claim 3, which is characterized in that a concentration of 6.25mg/mL-100mg/ of the water extract ML, a concentration of 0.3125mg/mL-5mg/mL of the alcohol extract.
5. application as claimed in claim 4, which is characterized in that when water extract is 100mg/mL, to anthrax bacteria, white rot The bacteriostasis rate of bacterium and ash arrhizus bacteria is 40.40%, 74.87% and 37.50%;As a concentration of 5mg/mL of alcohol extract, to grey mold Germ bacteriostasis rate is 97.13%, and 100% is up to white rot bacterium, anthrax bacteria, Aspergillus carbonerius germ inhibiting rate;Work as alcohol extracting During a concentration of 2.5mg/mL of object, to the bacteriostasis rates of 4 kinds of pathogens more than 85.5%;As a concentration of 5mg/mL of alcohol extract, It is respectively 96.30%, 94.33% and to carbendazim sensitivity anthrax bacteria bacterial strain FJZZ-62, coll-9, coll-20 bacteriostasis rate 96.88%, 100% is up to carbendazim highly resistance anthrax bacteria bacterial strain FJND-9, GZSD-89 inhibiting rate, the suppression to FJND-40 Rate processed also reaches 96.09%, and carbendazim sensitivity ash arrhizus bacteria bacterial strain GXGL-7, GXNN-7 germ bacterium bacteriostasis rate is up to 100%, it is 96.21% to GXNN-6 bacteriostasis rates, it is equal to carbendazim highly resistance ash arrhizus bacteria bacterial strain HBLF-10, GXZY-7 inhibiting rate Up to 100%, to the inhibiting rate of GXZY-4 up to 97.01%.
6. application as claimed in claim 4, which is characterized in that the alcohol extract generates OTA to Aspergillus carbonerius germ to be had Apparent inhibiting effect, as a concentration of 5mg/mL of alcohol extract, it is most apparent that OTA generates lag.
CN201711325207.6A 2017-12-13 2017-12-13 Asarum sieboldii extract and application thereof as plant antibacterial Expired - Fee Related CN108142443B (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111778165A (en) * 2020-08-11 2020-10-16 哈尔滨工业大学 Aspergillus niger DFY1 and application thereof

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101027990A (en) * 2007-03-13 2007-09-05 西北农林科技大学无公害农药研究服务中心 Bactericidal use of asarone for preventing and treating plant diseases caused by plant pathogenic bacteria
CN105941513A (en) * 2016-06-26 2016-09-21 合肥慧谷农业科技有限公司 Plant bactericide and preparation method thereof

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101027990A (en) * 2007-03-13 2007-09-05 西北农林科技大学无公害农药研究服务中心 Bactericidal use of asarone for preventing and treating plant diseases caused by plant pathogenic bacteria
CN105941513A (en) * 2016-06-26 2016-09-21 合肥慧谷农业科技有限公司 Plant bactericide and preparation method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
刘海燕: "细辛挥发油抗植物病原真菌活性及作用机理研究", 《中国优秀博硕士学位论文全文数据库 (硕士)医药卫生科技辑》 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111778165A (en) * 2020-08-11 2020-10-16 哈尔滨工业大学 Aspergillus niger DFY1 and application thereof
CN111778165B (en) * 2020-08-11 2022-10-25 哈尔滨工业大学 Aspergillus niger DFY1 and application thereof

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