Summary notes – The cultures and the nutritional variation PDF

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Summary notes – The cultures and the nutritional variation Extinction jars for the cultivation and isolation of Mycobacterium, specifically Mycobacterium tuberculosis from clinical specimens. LJ medium was originally formulated by Lowenstein who incorporated congo red and malachite green to inhibit unwanted bacteria. The present formulation comprises of a glycerated eggbased medium and is based upon Jensen’s modification. Jensen modified Lowenstein’s medium by altering the citrate and phosphate contents, eliminating the congo red dye and by increasing the malachite green concentration. Gruft further modified L. J. Medium with the addition of penicillin, nalidixic acid and ribonucleic acid (RNA) to increase selectivity. This medium supports the growth of a wide variety of Mycobacteria and can also be used for niacin testing. Composition of Lowenstein Jensen (LJ) Media Ingredients Amount Potato Flour 30.0gm L- Asparagine 3.6gm Monopotassium Phosphate 2.4gm Magnesium Citrate 0.6gm Malachite Green 0.4gm Magnesium Sulfate 0.24gm Glycerol 12ml Egg Base 1000ml Lowenstein Jensen, Gruft Modification is the same as LJ Medium with the addition of: Nalidixic acid 56.0mg Penicillin 52.8mg RNA 0.05mg

Principle of Lowenstein Jensen (LJ) Media L-Asparagine and Potato Flour are sources of nitrogen and vitamins. Monopotassium Phosphate and Magnesium Sulfate enhance organism growth and act as buffers. Malachite green prevents the growth of the majority of contaminants surviving decontamination of the specimen while encouraging the growth of Mycobacteria. Egg Suspension provides fatty acids and protein required for the metabolism of Mycobacteria. When heated, the egg albumin coagulates, thus providing a solid

Variation and the candles characteristics and microscopy). Limitations of Lowenstein Jensen (LJ) Media It is recommended that biochemical and/or serological tests be performed on colonies from pure culture for complete identification. LJ Media require incubation in a 5-10% CO2 atmosphere in order to recover Mycobacteria. Mycobacteria, for unknown reasons, are not recovered well from candle extinction jars.

surface for inoculation. Glycerol serves as a carbon source and is favorable to the growth of the human type tubercle bacillus while being unfavorable to the bovine type. In Gruft method, Penicillin and Nalidixic acid along with malachite green prevents growth of the majority of contaminants surviving decontamination of the specimen while encouraging earliest possible growth of Mycobacteria. RNA acts as stimulant and help to increase the isolation rate of Mycobacteria.

Preparation of Lowenstein Jensen (LJ) Media Dissolve 37.3 g of the medium in 600 mL of purified water containing 12 mL of glycerol. Heat with frequent agitation to completely dissolve the medium. Autoclave at 121°C for 15 minutes. Prepare 1000 mL of a uniform suspension of fresh eggs under aseptic conditions. Avoid whipping air into suspension during the collection and mixing. Aseptically mix the 1000 mL of egg suspension with 600 mL of the sterile Lowenstein-Jensen Medium cooled to 50 – 60°C, avoiding air bubbles. Dispense the finished medium into sterile screw-cap test tubes. Place the tubes in a slanted position and heat at 85°C for 45 minutes. Result Interpretation of Lowenstein Jensen (LJ) Media Result Interpretation of Lowenstein Jensen (LJ) Media Cultures should be read within 5 to 7 days after inoculation and once a week thereafter for up to 8 weeks. The typical colonies are non pigmented, rough, dry on LJ medium. The green color of the medium is due to the presence of malachite green which is one of the selective agents to prevent growth of most other contaminants. Rapid growers have mature colonies within 7 days; slow growers require more than 7 days for mature colony forms. Pigment production: White, cream or buff = Nonchromogenic (NC) Lemon, yellow, orange, red = Chromogenic (Ch)

Uses of Lowenstein Jensen (LJ) Media It is used for the diagnosis of Mycobacterial infections. It is used for testing antibiotic susceptibility of isolates. It is also used for differentiating different species of mycobacterium (by colony morphology, growth rate, biochemical...