[go: up one dir, main page]

CN2646712Y - Quick test sheet paper for fungus and microzyme - Google Patents

Quick test sheet paper for fungus and microzyme Download PDF

Info

Publication number
CN2646712Y
CN2646712Y CN 03274715 CN03274715U CN2646712Y CN 2646712 Y CN2646712 Y CN 2646712Y CN 03274715 CN03274715 CN 03274715 CN 03274715 U CN03274715 U CN 03274715U CN 2646712 Y CN2646712 Y CN 2646712Y
Authority
CN
China
Prior art keywords
utility
model
cultivating
microzyme
epiphragma
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.)
Expired - Fee Related
Application number
CN 03274715
Other languages
Chinese (zh)
Inventor
卢新
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Guangzhou Oasis Biochemistry Technology Co.,Ltd.
Original Assignee
OASIS BIOCHEMISTRY RESEARCH CENTER
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by OASIS BIOCHEMISTRY RESEARCH CENTER filed Critical OASIS BIOCHEMISTRY RESEARCH CENTER
Priority to CN 03274715 priority Critical patent/CN2646712Y/en
Application granted granted Critical
Publication of CN2646712Y publication Critical patent/CN2646712Y/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Images

Landscapes

  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)

Abstract

The utility model relates to a quick testing slip for the mildew and the microzyme and belongs to the microbiology testing art domain. The utility model consists of an upper velum which is provided with sop gel powder with enzyme visualization reagent in the bottom surface and a cultivating slice which absorbs the cultivating liquid. The utility model has a better testing effect compared with the prior art; the utility model is convenient to be operated and leaves out a great of assisting works such as preparing the substrate and the disinfection and cleaning of the cultivating device; the utility model saves the cultivating time of the mildew and the microzyme and can sample and detect in any time; and the utility model will not be limited by the environment, the experimental device and the technical staff.

Description

The mould and the saccharomycetic quick test scraps of paper
(1) technical field
Technical field under the utility model is a microbiological Test, relates to mould and saccharomycetic a kind of quick test articles for use.
(2) background technology
The classic method of mould and saccharomycete check has: fall flat band method.Method is that the starting material of the preparation nutrient culture media that will be taken by weighing are put into water and boiled moltenly, treats that nutrient culture media is cooled to about 45 ℃, inserts sample liquid in the double dish, pour nutrient culture media into, keep flat and be cooled to flat board, thermophilic is observed, is counted after cultivating a week down, record mould and saccharomycetic growing state.
The operated in accordance with conventional methods complex steps will be done a large amount of auxiliary works before and after mould and saccharomycete are cultivated, count, cultivate vessel etc. as preparation nutrient culture media, sterilization, cleaning, and is very high to the requirement of experimental implementation technology.Temperature control requirement is rigorous, and incubation time is long, and the cycle reached about 1 week.
(3) summary of the invention
1, technical matters to be solved by this invention:
For solve described in the background technology to the existing problem of mould and saccharomycete check aspect, it is short to design a kind of easy and simple to handle, proving time, the disposable check scraps of paper are used for mould and saccharomycete being carried out quick test, the purpose of this utility model that Here it is.
2, the technical solution used in the present invention:
The utility model is made up of last epiphragma and cultivation sheet.Last epiphragma coated on bottom side cloth contain the water absorbent gel powder of enzyme developer, be waterproof and breathable, the transparent membrane that has graticule line, the tape square line is to observe counting for convenience.Cultivating sheet is the scraps of paper that adsorbed liquid medium, and it is bonded at below the epiphragma.In order to carry epiphragma and to cultivate sheet, forms an excellent environment that helps mould and saccharomycete growth, prevent the moisture turnover, be preferably in the egative film that one deck waterproof and breathable is arranged below epiphragma and the cultivation sheet, egative film is preferably made by synthetic material.
With the utility model mould and saccharomycetic check are realized by following process.
1) will check scraps of paper level to be placed on the table top, open epiphragma, draw sample stoste or dilution 1mL, and evenly be added to and cultivate on the sheet, will go up epiphragma then gently and put down, leave standstill 5 minutes with the sterilization suction pipe.
2) push gently in the middle of the grid zone with finger, moisture is evenly distributed in scraps of paper grid zone, and bubble is driven away.
3) the check scraps of paper that will add sample lie in the 28-35 ℃ of incubator and cultivated 48-72 hour.
4) amplification by the enzyme chromogenic reaction, mould and saccharomycete will show blue spot in growth on the scraps of paper after 24 hours, bigger or a bit diffusion of the spot that mold colony shows, yeast colony is then less and slick and sly, and many moulds can present itself distinctive color in late stage of culture.Select the scraps of paper of clump count moderate (10-100) to count, be mould and saccharomycetic number in every gram (or milliliter) sample after multiply by extension rate.
3, beneficial effect of the present invention:
A large amount of auxiliary works such as cleaning treatment of preparation nutrient culture media, sterilization and cultivation vessel have been saved, at any time can begin to carry out sampling Detection, and easy and simple to handle, by the amplification of enzyme developer, mould and saccharomycetic bacterium colony are clearly displayed in advance.Also saved mould and saccharomycetic incubation time, traditional multistep culture identification process be simplified to one the step finish, incubation time shortens to 48-72 hour by a week.Be not subjected to the restriction of many-sided conditions such as environment, experimental facilities and technician.
(4) accompanying drawing and embodiment
Fig. 1 is the synoptic diagram directly perceived according to a kind of pattern (when raising epiphragma) that the utility model proposes.
Fig. 2 is a cut-open view of the present utility model.
With reference to accompanying drawing, present embodiment is made up of following each several part:
1---epiphragma in the representative,
2---sheet is cultivated in representative,
3---represent egative film.
In the present embodiment: going up epiphragma 1 is that the bottom surface has been coated with the water absorbent gel powder that contains the enzyme developer, the waterproof and breathable, the transparent membrane that have graticule line, its length * wide size is 75 millimeters * 65 millimeters, and the surface is printed on 16 grids, and the size of each grid is 11 millimeters * 11 millimeters; Cultivating sheet 2 is the scraps of paper that adsorbed liquid medium, and its length * wide size is 46 millimeters * 46 millimeters; Egative film 3 is made waterproof and breathable by synthetic material.Last epiphragma 1, cultivation sheet 2 and egative film 3 usefulness viscose glues stick together.

Claims (3)

1, a kind of mould and the saccharomycetic quick test scraps of paper is characterized in that it is coated with last epiphragma that contains enzyme developer water absorbent gel powder and the cultivation sheet that has adsorbed liquid medium and forms by the bottom surface.
2, the mould according to claim 1 and the saccharomycetic quick test scraps of paper is characterized in that epiphragma is waterproof and breathable, the transparent membrane that has graticule line.
3,, under it is characterized in that epiphragma and cultivating sheet egative film is arranged according to claim 1,2 described moulds and the saccharomycetic quick test scraps of paper.
CN 03274715 2003-09-26 2003-09-26 Quick test sheet paper for fungus and microzyme Expired - Fee Related CN2646712Y (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 03274715 CN2646712Y (en) 2003-09-26 2003-09-26 Quick test sheet paper for fungus and microzyme

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 03274715 CN2646712Y (en) 2003-09-26 2003-09-26 Quick test sheet paper for fungus and microzyme

Publications (1)

Publication Number Publication Date
CN2646712Y true CN2646712Y (en) 2004-10-06

Family

ID=34302041

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 03274715 Expired - Fee Related CN2646712Y (en) 2003-09-26 2003-09-26 Quick test sheet paper for fungus and microzyme

Country Status (1)

Country Link
CN (1) CN2646712Y (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101914608A (en) * 2010-08-09 2010-12-15 曹莹莹 Letter pad-type culture medium for rapidly and quantitatively testing flora amount
CN101570733B (en) * 2009-05-12 2011-05-18 山西省食品工业研究所 Method for culturing and separating acid-resistant mould fungi
CN102471747A (en) * 2009-07-14 2012-05-23 大日本印刷株式会社 Microorganism culture sheet and manufacturing method therefor
CN103343158A (en) * 2013-07-20 2013-10-09 吉林农业大学 Detection paper piece for clostridium perfringens, preparation method and application for same
CN105483204A (en) * 2015-12-25 2016-04-13 贵州勤邦食品安全科学技术有限公司 Detection vessel for rapidly detecting moulds and yeasts and preparation method
CN106811403A (en) * 2017-01-22 2017-06-09 贵州勤邦食品安全科学技术有限公司 A kind of test piece of quick detection bacillus cereus and preparation method thereof, detection method

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101570733B (en) * 2009-05-12 2011-05-18 山西省食品工业研究所 Method for culturing and separating acid-resistant mould fungi
CN102471747A (en) * 2009-07-14 2012-05-23 大日本印刷株式会社 Microorganism culture sheet and manufacturing method therefor
CN102471747B (en) * 2009-07-14 2014-04-02 大日本印刷株式会社 Microorganism culture sheet and manufacturing method therefor
CN101914608A (en) * 2010-08-09 2010-12-15 曹莹莹 Letter pad-type culture medium for rapidly and quantitatively testing flora amount
CN103343158A (en) * 2013-07-20 2013-10-09 吉林农业大学 Detection paper piece for clostridium perfringens, preparation method and application for same
CN103343158B (en) * 2013-07-20 2014-05-14 吉林农业大学 Detection paper piece for clostridium perfringens, preparation method and application for same
CN105483204A (en) * 2015-12-25 2016-04-13 贵州勤邦食品安全科学技术有限公司 Detection vessel for rapidly detecting moulds and yeasts and preparation method
CN106811403A (en) * 2017-01-22 2017-06-09 贵州勤邦食品安全科学技术有限公司 A kind of test piece of quick detection bacillus cereus and preparation method thereof, detection method

Similar Documents

Publication Publication Date Title
JP7506986B2 (en) Self-contained anaerobic environment generating culture device and method of use
CN105483204A (en) Detection vessel for rapidly detecting moulds and yeasts and preparation method
CN107532121A (en) Culture apparatus for anaerobe
CN2646712Y (en) Quick test sheet paper for fungus and microzyme
CN101319248A (en) Method for directly preparing microorganism testing slice with commercial product culture medium dry powder
KR101903642B1 (en) Culture apparatus for lactic acid bacteria
CN104911243A (en) Solid culture medium for inoculating liquid samples and culture method
CN101693870A (en) Culture method and device of plant rhizosphere soil microorganism
FR2993573A1 (en) METHOD FOR ISOLATING MICROORGANISMS ON A CULTURE MEDIUM AND DEVICE THEREFOR
CN107532126A (en) Film culture apparatus with carbon dioxide generation agent
CN2611903Y (en) Microbe assaying sheet
CN202164305U (en) Quick detection card for enterobacter sakazakii in dairy products
CN201241126Y (en) Disposable microorganism test board
CN109371101A (en) A kind of staphylococcus aureus chromogenic culture medium and detection testing piece
CN107815437A (en) A kind of method of sweet potato black rot pathogen rapid, high volume production spore
CN210560383U (en) Culture apparatus of anaerobe
CN203117162U (en) Integrated membrane biosensor for quickly detecting escherichia coli
CN201933094U (en) Bacterium detecting device
CN106811403A (en) A kind of test piece of quick detection bacillus cereus and preparation method thereof, detection method
CN2908517Y (en) Test chip for pathogenic microorganism in food
CN118064250A (en) A multifunctional microbial screening and cultivation system
CN103290096B (en) The method of qualification mould starch-splitting ability
CN2169629Y (en) Disposable micro porous filtering and cultivating device
CN218290926U (en) Adhesion type rapid quantitative disc for number of bacteria in water
CN101307292A (en) Easy and rapid screening method for bioactive substance

Legal Events

Date Code Title Description
C14 Grant of patent or utility model
GR01 Patent grant
EE01 Entry into force of recordation of patent licensing contract

Assignee: Guangzhou Oasis Biochemistry Technology Co., Ltd.

Assignor: Oasis Biochemistry Research Center

Contract fulfillment period: 2007.6.13 to 2013.9.25

Contract record no.: 2009440001013

Denomination of utility model: Quick test sheet paper for fungus and microzyme

Granted publication date: 20041006

License type: Exclusive license

Record date: 20090806

LIC Patent licence contract for exploitation submitted for record

Free format text: EXCLUSIVE LICENSE; TIME LIMIT OF IMPLEMENTING CONTACT: 2007.6.13 TO 2013.9.25; CHANGE OF CONTRACT

Name of requester: GUANGZHOU OASIS BIOCHEMISTRY TECHNOLOGY CO., LTD.

Effective date: 20090806

DD01 Delivery of document by public notice

Addressee: Lu Xin

Document name: Notification to Pay the Fees

DD01 Delivery of document by public notice

Addressee: Oasis Biochemistry Research Center Lu Xin

Document name: Notification of Termination of Patent Right

ASS Succession or assignment of patent right

Owner name: GUANGZHOU OASIS BIOCHEMISTRY TECHNOLOGY CO., LTD.

Free format text: FORMER OWNER: OASIS BIOCHEMISTRY RESEARCH CENTER

Effective date: 20120104

C41 Transfer of patent application or patent right or utility model
COR Change of bibliographic data

Free format text: CORRECT: ADDRESS; FROM: 510665 GUANGZHOU, GUANGDONG PROVINCE TO: 510663 GUANGZHOU, GUANGDONG PROVINCE

TR01 Transfer of patent right

Effective date of registration: 20120104

Address after: 902 room 7, No. 510663, 1st floor, science Avenue, Guangzhou hi tech Industrial Development Zone, Guangdong, China

Patentee after: Guangzhou Oasis Biochemistry Technology Co.,Ltd.

Address before: 308, room 510665, west seat, Tong Li building, 491 West Zhongshan Road, Guangzhou, Guangdong

Patentee before: Oasis Biochemistry Research Center

DD01 Delivery of document by public notice

Addressee: Lu Xin

Document name: Notification of Passing Examination on Formalities

C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20041006

Termination date: 20120926