Organic Name Reactions for the students and aspirants of Chemistry12th.pptx
Ideal charecteristics to construct a plant tissue culture
1. Presented by
NILANJAN ADHIKARI
B.PHARM, 4th year 7th SEM
REG. NO.- 142420210054 OF 2014-15
ROLL NO- 24201914054
UNDER THE GUIDENCE
OF
MR. SUPRIYA DATTA (SR. ASST. PROF.)
OF
BENGAL COLLEGE OF PHARMACEUTICAL SCIENCES &
RESEARCH
AFFILIATED TO
MAULANA ABUL KALAM AZAD UNIVERSITY OF TECHNOLOGY (W.B)
2017
2. DEFINATION OF PLANT TISSUE CULTURE
LOCATION
IDEAL UNIT FOR DECORATE PLANT TISSUE CULTURE LAB
PURPOSES FOR THATS CHEMBER
ESTIMATE DIMENTION
DIAGRAMMATIC CONSTRUCTION
GLASSWARE & OTHER EQUIPMENTS
ESTIMATE BUDJET
SHORT QUOTE VIDEO OF PROCESS OF “PLANT TISSUE
CULTURE”
CONCLUSION
REFERENCE
3. Plant tissue culture is a collection of techniques used
to maintain or grow plant cells, tissues or organs under
sterile conditions on a nutrient culture medium of
known composition.[1]
Plant tissue culture is widely used to produce clones
of a plant in a method known as Micro propagation.[3]
3
4. The location shall confirm to the land use plan of
the area.
The building should be located away from
sources of contamination such as soil mixing area,
storage etc.
The site shall be accessible to service roads,
water supply and electric lines.
The site shall be well drained.
4
5. A research facility should have at least four
chamber[1]:
Washing Area,
Media Preparation Room,
Sterile Area,
Growth/Culture Room,
5
6. Washing area [6]
for glassware washing
storage and
autoclaving.
Media preparation room
for media preparation
Sterile area
for aseptic manipulation
Growth & culture room
to maintain cultures under suitable
environmental conditions
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7. [4],[6]
The glassware washing area shall be located near the
sterilization and media preparation areas.
Washing sink(45cm x 60cm) can be fitted in one side
of Room and should be acidic and alkali resistant.
Room also provided with Bucket, detergent , mug and
also Plastic tray to kept washed Media bottles and
sterilized media.
Room provided with water line and electricity line.
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8. The area shall be provided with working tables which should be up to
1.2 m wide and the height should be 850 mm – 900 mm. [5],[6]
Table top shall be covered with materials which are easily cleaned and
which will stand disinfectant solution.
Water source and glassware storage area shall be provided.
Room contains double distilled water unit , pH meter, buffer solution,
electronic balance , cooling freeze, measuring cylinder, magnetic
stirrer, pipette, hot plate, media bottle.
Room should contains the stock A,B,C,D, E and F solution with
required chemicals such as sucrose, adenine sulphate ,innositol , agar-
agar( solidifying agent) etc
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9. [3],[5]
The room should have One autoclave(vertical or horizontal)
or cooker with well ventilated exhaust fan.
Also having tools for support while placing the media
bottles in autoclave or cooker for sterilization.
The bottles should sterilized At 1200 C at 15 lb. for 1 hrs.
It contains wrapping paper to wrap and the rubber to tight
the inoculating dishes for sterilization.
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10. The floor of room covered with tiles to facilitate proper
cleaning. [2],[6],[9]
Room contains the laminar air flow cabinet with installation
of a HEPA (high efficiency particulate air) filter for filtered
air supply.
It also requires sodium hypochlorite, mercuric chloride and
70% alcohol for surface sterilization .
It requires forceps , scalpel, sterile bottles, sterile dishes,
spirit lamp , cotton and hand care etc.
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11. The width of the racks should be 405 mm to 1 m. The distance
between each layer of the racks should be not less then 455
mm. [4],[6],[7]
Photoperiod racks with culture bottles shall be provided. we
mostly operate light intensity with a standard day length of 16
hours and 8 hour dark regime.
Temperature is maintained at a standard 25 + 20 C with 1.5 ton
window A.C. to creating the controlled environment condition.
Light intensity required about 200 lux to 1600 lux for growth
of culture.
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12. Bottle washing machine and autoclave. [8],[10]
Freezer and Rotary shaker.
Multipurpose Magic stove.
Weighing balance, thermometer .
Magnetic stirrer and Digital pH meter.
Laminar air flow with U.V. tube .
Racks-photoperiodic culture Glass bed sterilizer
Air conditioner with Stabilizer and Micro air oven etc.
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13. Glass bottle, Petridis, burette, funnel. [9]
Beakers and pipettes.
conical flask with screw cap.
Graduated measuring cylinder
Spatula, scalpel and forceps
Wrapping paper and bucket, gloves etc.
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15. General Chemical Cost
Glasswares - 10,000-15,000/-
All chemicals – 20,000/- (Depending)
Aluminium racks – 5,000/- (Depending on Area)
Other requirement for laboratories – 25,000/-
Instrumentation
Water Purifier System – 15,000/-
Electronic Balance – 1,200/-
pH Meter – 10,000/-
Hot Plate – 1,000/-
Refrigerator – 15,000-25,000/-
Laminar Air Flow – 35,000/-
Pipette – 10,000/-
Autoclave – 30,000/-
Computer – 18,000/-
Microscope – 7000/- cntd…
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16. PERSONNEL with needed basic Qualification
Laboratory In charge (ADMIN)
Bsc.(Bio-tech, Micro-bio) / B.Pharm / B. Tech(Bio-tech)
Tools Operator
Any Computer certifiedperson(With Experienced in field)
Laboratory Technician
Bsc(Chem)/D.Pharm
***<N.B. Salary of stuff will be as per requite authority>***
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18. This PROJECT work helps us to construct an ideal
plant tissue culture laboratory where plantlet
regeneration will takes place from explants by
micro propagation techniques.
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20. 6. A practical guide to setting up an IVF lab, Embryo culture
systems and running the unit, Jaypee Brothers Medical
Publishers ISBN 978-93-50905-16-6,1st edition,2013
7. “Plant Tissue Culture: Current Status and Opportunities”
Published by INTECH [open science|open minds], World’s
largest Science, Technology & Medicine open Access book
Publisher, 2013
8. W.C. Evans, Trease and Evans Pharmacognosy, “Plant cell
and tissue culture; biochemical conversions; clonal
propagation” ISBN: 978-0-7020-2617-1 An imprint of Elsevier
WB Saunders Company Limited 1996, Harcourt Publishers
Limited 1999, 2002
9. George, Edwin F.; Hall, Michael A.; De Klerk, Geert-Jan, eds.
(2008). Plant propagation by tissue culture 1. The background
(3rd ed.). Springer.
10. Yadav, R.; Arora, P.; Kumar, D.; Katyal, D.; Dilbaghi, N.;
Chaudhury, A. (2009). "High frequency direct plant
regeneration from leaf, internode, and root segments of Eastern
Cottonwood (Populus deltoides)". Plant Biotechnology
Reports. 3 (3): 175–182. doi:10.1007/s11816-009-0088-5
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