deepak yadav staining

37

Upload: deepak-yadav-dee-pee

Post on 21-Jul-2015

72 views

Category:

Education


0 download

TRANSCRIPT

Page 1: deepak yadav staining
Page 2: deepak yadav staining
Page 3: deepak yadav staining

Most micro-organisms can’t be observed properly

under the light microscope because they are transparent

& appear colourless .

We must prepare them for the observation. One of the

ways it can be done is by staining.

Page 4: deepak yadav staining
Page 5: deepak yadav staining

*Acidic stain:- They have negatively charged groups and stain the

cytoplasmic components of the cells which have positive charge.

e.g:- picric acid, rose bengal, acid fuchsin, eosin.

* Basic stain:- They have +vely charged groups and stain cytoplasmic

components of the cells which have negative charge (nucleus).

Eg:- methylene blue, crystal violet, safranine.

* Neutral stain:- They are formed by mixing together aquous solution of

certain acidic & basic dyes. The colouring matter in them is both

negatively & positively charged components.

Page 6: deepak yadav staining

Staining solution are prepared by dissolving a particular stain in either distilled water or alcohol.

The stain is applied to smear for a definite time then washed dried & examine under the microscope.

Page 7: deepak yadav staining

Depending upon how the stain reacts with the specimen,

staining are of 2 types :-

Positive staining :- it involves the sticking of the stain to the specimen and giving it a color.

Negative staining :- they stain background and doesnotstain the specimen.

Page 8: deepak yadav staining

Negative staining technique is advantageous for 2 reasons;

* Microbial cells appear less shriveled or distorted because heat

fixation is not carried out,

* Capsulated bacteria that are difficult to stain can be

observed by this technique.

Page 9: deepak yadav staining
Page 10: deepak yadav staining
Page 11: deepak yadav staining
Page 12: deepak yadav staining
Page 13: deepak yadav staining
Page 14: deepak yadav staining
Page 15: deepak yadav staining
Page 16: deepak yadav staining
Page 17: deepak yadav staining
Page 18: deepak yadav staining
Page 19: deepak yadav staining
Page 20: deepak yadav staining
Page 21: deepak yadav staining
Page 22: deepak yadav staining
Page 23: deepak yadav staining
Page 24: deepak yadav staining
Page 25: deepak yadav staining
Page 26: deepak yadav staining
Page 27: deepak yadav staining

The most commonly used endospore stain is the Schaeffer-fultonstain.

Malachite green, the primary stain is applied to the heat fixed smear & heated to steaming for about 5 minutes. The heat helps the stain to

penetrate the endospore wall.

The preparation is washed for about 30 sec with water to remove the extra stains.

Then safranine , a counter stain is applied to the smear to stain the portions of the cell other than the endospore.

The endospore appear green within red or pink cell.

Page 28: deepak yadav staining
Page 29: deepak yadav staining
Page 30: deepak yadav staining
Page 31: deepak yadav staining
Page 32: deepak yadav staining
Page 33: deepak yadav staining
Page 34: deepak yadav staining

Generally all the algal cells contain pigments which specify

them widely therefore they donot require any specific stain.

They are generally mounted with glycerine.

Sometimes safranine is used to stain algal cells in order to

observe the clarity of the cells.

Page 35: deepak yadav staining
Page 36: deepak yadav staining

References

- Microbiology :- Presscott , Harley , Klein .-Principles of Microbiology :- Ronald M. Atlas .- Basic & Applied Microbiology :- K. R. Aneja .

- www.google.com- Wikipedia .

Page 37: deepak yadav staining