
Tuberculosis, popularly known as TB disease, is caused by the bacteria Mycobacterium tuberculosis. It is a contagious disease that primarily affects the lungs but can affect other body parts as well. Löwenstein-Jensen (LJ) Medium is the basic medium for the isolation and identification of Mycobacterium species, specifically Mycobacterium tuberculosis. In this blog, let’s discuss the basic aspects of mycobacteriology, specifically Mycobacterium and Löwenstein-Jensen (LJ) Medium. As a veteran microbiologist, you must have seen the pivotal place LJ Medium holds in clinical diagnostics and in the laboratory, most notably with the notoriously recalcitrant Mycobacterium genus.
Solid Culture Media used for isolation and cultivation of Mycobacteria are either egg-based or agar-based. Of the egg-based media, Lowenstein Jensen Medium is most commonly used. LJ Medium is especially formulated to enable the slow as well as the fastidious growth of Mycobacteria. It has a distinct composition that presents a nutrient medium that significantly discourages the growth of contaminant bacteria, enabling the selective isolation of Mycobacterium.
Originally this medium was formulated by Lowenstein (the first part solved). Lowenstein composition contains congo red and malachite green dyes. Then Jensen (second part resolved) modified the Lowenstein composition by altering the citrate and phosphate contents; he also eliminated the congo red dye and raised the concentration of the malachite green dye. And that’s not enough; then Gruft further modified LJ Medium with the addition of two antimicrobics to increase selectivity (then why is it not Löwenstein-Jensen Gruft (LJG) Medium?).
This medium supports the growth of a wide variety of Mycobacteria and can also be used for niacin testing.
Egg-based media contain whole eggs or egg yolk, potato flour, and salts and are solidified by inspissation.
Let’s discuss the most important components that contribute to the efficacy of LJ Medium:
| Ingredients | Gms / Ltr |
| L-Asparagine | 3.60 |
| Potassium dihydrogen phosphate | 2.40 |
| Magnesium sulphate | 0.24 |
| Magnesium citrate | 0.60 |
| Potato starch, soluble | 30.00 |
| Malachite green | 0.40 |
Eggs are the fundamental component of LJ Medium, which offers a good source of proteins, lipids, and growth factors. They especially provide the necessary fatty acids, albumin, and globulins, all of which play a pivotal role in Mycobacteria growth. The original medium solid matrix is formed by coagulation of the eggs during inspissation.
Asparagine is an easily available source of nitrogen, an essential requirement in bacterial protein synthesis.
This part offers inorganic salts required for bacterial metabolism.
It normally includes:
Some formulations include potato flour, which provides starch and additional growth factors.
It can improve the consistency and nutrient availability of the medium.
It is a selective agent that prevents the growth of most contaminating bacteria. Mycobacterium species are relatively resistant to malachite green, allowing them to grow preferentially. It also serves as a pH indicator. Formation of blue zones indicates a decrease in pH by gram-positive contaminants (e.g. Streptococci) and yellow zones indicates dye destruction by gram-negative bacilli. Proteolytic contaminants cause localized or complete digestion of medium.
This medium also contains Penicillin and Nalidixic acid, which, along with malachite green, prevents the growth of the majority of contaminants surviving decontamination of the specimen while encouraging the earliest possible growth of Mycobacteria.
Careful formulation of LJ Medium is required for it to be effective. The important processes are:
LJ Medium in the Contemporary Microbiology Laboratory
While Molecular Diagnostics have revolutionized Mycobacteriology, LJ Medium remains a valuable tool for:
At TM Media, we understand the importance of Quality-assured Culture Media for accurate diagnosis. Check out our range of over 2000 Dehydrated Culture Media.
The LJ Medium, with its highly optimized composition, continues to be a major tool employed in the fight against mycobacterial infections. With thorough knowledge of its components and proper use, microbiologists are able to determine accurate and reliable results in their research and diagnostic processes.
Until we meet again, keep culturing!
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