Caulobacter Medium

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SKU:
M1661
For cultivation of Caulobacter species.


Caulobacter Medium is recommended for cultivation of Caulobacter species.

Composition**

Ingredients Gms / Litre
Peptone 2.000
Yeast extract 1.000
Magnesium sulphate heptahydrate 0.200
Agar 10.000

Final pH ( at 25°C): 7.0±0.2

**Formula adjusted, standardized to suit performance parameters

Directions

Suspend 13.10 grams (the equivalent weight of dehydrated powder per litre) in 1000 ml distilled water. Heat to boiling to dissolve the medium completely. Sterilize by autoclaving at 15lbs pressure (121°C) for 15 minutes. Mix well and pour into sterile Petri plates.

Principle And Interpretation

Caulobacter is a gram-negative bacterium, which resembles the aerobic, chemoheterotrophic Pseudomonades, with which they often share their natural habitats. Caulobacter generally live in a dilute aquatic environment where the most common limiting factor is phosphorus, an essential element for healthy growth. Caulobacter belongs to the group of dimorphic prosthecate bacteria (DPB) where reproduction takes place in an asymmetric manner rather than by binary fission. The daughter cells produced are morphologically and behaviorally different from each other, which makes them a suitable model to study regulation of cell cycle and cellular differentiation. Lack of nutrients makes Caulobacter to dramatically elongate its stalk up to 30 times longer than those in phosphrous-rich medium (1). They are tolerant to prolonged nutrient scarcity, which provides a dependable physiological basis for their enrichment (2).

Caulobacter Medium was developed by using the formula of Poindexter (4), by addition of solidifying agent, agar. It is recommended for cultivation of Caulobacter species (3). This medium is supplied as Medium 28 for Caulobacter by Pasteur Institute (5). This medium was also used by Qi and Bernd (6) to study polyhydroxybutyrate biosynthesis. The importance of employing dilute media was discovered during the first reported isolation of Caulobacter by Loeffler (7).

Caulobacter Medium is low in nutrient concentration. Growth of Caulobacter in rich media or in severely unbalanced media is extremely poor if it occurs and the cells are structurally fragile and morphologically aberrant. This medium has peptone and yeast extract as ingredients, which act as source of nitrogen, amino acids and vitamins for the growth of organisms. Magnesium sulphate supplies essential ions for Caulobacter growth.

Quality Control

Appearance Cream to yellow homogeneous free flowing powder

Gelling Firm, comparable with 1.0% Agar gel.

Colour and Clarity of prepared medium Light to medium amber coloured, clear to slightly opalescent gel forms in Petri plates

Reaction Reaction of 1.30 w/v aqueous solution at 25°C. pH : 7.0±0.2

pH 6.80-7.20

Cultural Response M1661: Cultural characteristics observed after an incubation at 30-35°C for 4-7 days.

Organism Growth
Caulobacter crescentus ATCC 15252 good-luxuriant
Caulobacter fusiformis ATCC 15257 good-luxuriant

Storage and Shelf Life

Store below 30°C in tightly closed container and the prepared medium at 2-8°C. Use before expiry date on the label.

Reference

  1. Gonin M., Quardoleus E. M., ODonnol D., Maddock J., and Brun Y. V.,2000, J. Bacteriol., 182:337
  2. Balows A., Truper H. G., Dworkin M., Harder W., Schleifer K. H., (Eds.), The Prokaryotes, 1992, 2nd Edition, Vol. III, Springer-Verlag.
  3. Atlas R. M., 2004, Handbook of Microbiological Media, 3rd Edition, CRC Press.
  4. Poindexter J. S., 1964, Bacteriol. Rev., 28:231
  5. Collection Institute Pasteur Medium Description, Institute Pasteur.
  6. Qi Qingsheng and Bernd H. A. Rehm, 2001, Microbiology, 147:3353
  7. Loeffler F., 1980, Bakteriol. Parasitenkd., 7:625-639.
More Information
Product Name Caulobacter Medium
SKU M1661
Product Type Regular
Physical Form Powder
Origin Animal
Packaging type HDPE
References 1. Atlas R. M., 2004, Handbook of Microbiological Media, 3rd Edition, CRC Press 2.Baird R.B., Eaton A.D., and Rice E.W., (Eds.), 2015, Standard Methods for the Examination of Water and Wastewater, 23rd ed., APHA, Washington, D.C. 3.Balows A., Truper H. G., Dworkin M., Harder W., Schleifer K. H., (Eds.), The Prokaryotes, 1992, 2nd Edition, Vol. III, Springer-Verlag. 4.Collection Institute Pasteur Medium Description, Institute Pasteur 5.Gonin M., Quardoleus E. M., ODonnol D., Maddock J., and Brun Y. V.,2000, J. Bacteriol., 182:337 6.Isenberg, H.D. Clinica Microbiology Procedures Handbook 2nd Edition.7.Jorgensen, J.H., Pfaller, M.A., Carroll, K.C., Funke, G., Landry, M.L., Richter, S.S and Warnock., D.W. (2015) Manual of Clinical Microbiology, 11th Edition. Vol. 1.8.Loeffler F., 1980, Bakteriol. Parasitenkd., 7:625-639.9.Poindexter J. S., 1964, Bacteriol. Rev., 28:23110.Qi Qingsheng and Bernd H. A. Rehm, 2001, Microbiology, 147:3353
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