Culture media are substances used to grow and maintain microorganisms in the laboratory. They typically consist of a mixture of nutrients and other substances that support the growth and metabolism of microorganisms. Culture media can be liquid, semisolid, or solid, and they can be tailored to the specific requirements of different types of microorganisms.
Culture media are an important tool in microbiology, as they allow scientists to isolate, identify, and study microorganisms in the laboratory. They are used in a wide range of applications, including the identification of pathogens, the production of biotechnology products, and the study of the biology and behavior of microorganisms.
There are many different types of culture media, including:
Nutrient media: These media contain a variety of nutrients, such as carbohydrates, proteins, and minerals, to support the growth of microorganisms.
Selective media: These media contain specific substances that inhibit the growth of certain types of microorganisms, allowing only certain types of organisms to grow.
Differential media: These media contain substances that allow different types of microorganisms to be distinguished based on their growth characteristics.
Enrichment media: These media contain substances that enhance the growth of certain types of microorganisms.
Culture media are an essential tool in microbiology and are used in a wide range of research and applied settings. They allow scientists to study the biology, behavior, and ecology of microorganisms and to identify and characterize new species. They also play a crucial role in the production of biotechnology products and in the diagnosis and treatment of diseases caused by microorganisms.
Deoxycholate Citrate Agar is an alteration of Leifson formula that is suggested for the identification of Salmonella as well as Shigella spp. It is comparable to deoxycholate agar however it is slightly more selective for enteric pathogens due to higher levels of both deoxycholate and citrate salts. The sodium deoxycholate pH range of 7.3 to 7.5 inhibits gram-positive bacteria. Citrate salts in the amount contained into the composition, act as inhibitors to gram-positive bacteria, as well as other intestinal organisms that are normal. This makes it an effective and selective media, commonly used to isolate intestinal pathogens.
Cary-Blair Transport Medium is simple, semi-solid, and non-nutritive medium that is used to collect and storage of samples of microbiological organisms. The low levels of nutrients in the medium aid in the life of the organisms, without multiplication. The semisolid consistency facilitates the ability to transport easily and the medium is able to be stored for up to a year after its preparation at temperatures of room temperature. Cary-Blair Transport Medium is a modification to Stuart’s Medium which is comprised of a more effective buffering system that replaces sodium glycerophosphate by organic phosphates. This new formulation helps prevent the growth of Enterobacteriaceae and aids in the long-term conservation for Salmonella as well as Shigella for extended durations. It is employed for the transport of clinical specimens believed to have enteric pathogenssuch as Shigella, Salmonella, Vibrio Cholerae, and Escherichia Coli O157 H7.
Loeffler Medium, a modified version of the 1887 Loeffler formula, is now called Loeffler Medium. Loeffler medium is a modified formula that Loeffler developed in 1887. It enhances primary and secondary isolation, and cultivates fastidious pathogenic microorganisms. After prolonged subculturing or prolonged incubation, Loeffler medium restores virulence as well as other identifying properties (microscopic/colonial). High serum levels are useful in determining organisms’ proteolytic activity. It can also be used to demonstrate pigmentation and ascospores.
Campylobacter blood agar (CVA), is a selective medium that allows for the primary isolation from stool specimens of Campylobacter Jejuni. Dekeyser et al. Dekeyser et al. reported that Campylobacter jejuni was isolated from patients suffering from diarrhea and acute gastroenteritis using a filtration method and a selective media with antimicrobials. Skirrow, however, reported that a select medium containing three antimicrobics was used for isolation. Blaser and colleagues reported that they were able to isolate C. jejuni from feces using a selective medium that contained four antimicrobials: amphotericin (vancomycin), polymyxin B and trimethoprim. Reller et al. in 1983 also introduced a better selective medium containing cefoperazone and Vancomycin. This combination of antimicrobials allowed for better suppression of normal fecal bacteria, thereby allowing for better isolation of C.jejuni from the fecal specimen.
Rosenow developed a medium that could be used to cultivate streptococci using a dextrose broth and brain tissue in 1919. Hayden modified Rosenow’s formula and found that crushed marble promoted the growth of dental pathogens. The current formulation uses infusions from calf brain instead of brain tissue, and disodiumphosphate has been replaced by calcium carbonate.
In 1979, Dr. A. Rambach invented and patented the first chromogenic medium for E.coli detection. This technology uses a color-based differentiation technique. It uses soluble colorless molecules, also known as chromogens. They are composed of a substrate that targets a specific enzyme activity and a chromophore. The chromophore can be released when the enzyme of the target organism cleaves the colorless, chromogenic conjugate.
Peptone Yeast Extract Broth Based Media are enriched nonselective media which include hemin and vitamin K to aid in the recovery of aggressive organisms like Prevotella Spp., Porphyromonas species, as well as the Bacteroides fragileis group.
MacConkey Sorbitol Agar is an adaptation of the formulation that was described by Rappaport and Henigh. It is selective and differential media for the detection of sorbitol-nonfermenting Escherichia coli serotype O157:H7 associated with hemorrhagic colitis. E. coli serotype O157:H7 is a human pathogen that is associated with hemorrhagic colitis which is caused by the actions of a Shiga-like toxins (SLT).
Thayer and Martin have reported improvement of the Chocolate Agar formulation that contained antimicrobics vancomycin and colistin, Nystatin. These ingredients were added to limit the growth of contaminants, inhibit the development of the saprophytic Neisseria sp. and to enhance the development of the pathogenic Neisseria. Martin and Lester have added an antibiotic, trimethoprim, which made them more selective. They also demonstrated to be effective in the fight against Proteus spp. Trimethoprim lactate refrains Proteus swarming. The resultant medium is known as Modified Thayer Martin. It’s a suitable and rich medium to isolate as well as cultivation of the Neisseria species. from mixed flora and suppression of other Gram-negative diplococci and gram-negative bacilli yeast and other gram-positive organisms.
Roantree et al introduced a medium for the isolation of streptococci from group A beta-hemolytic. The medium was enriched with yeast nucleic acids and maltose boosted the size of colonies and improved the clarity, sharpness and precision of the hemolytic zones created by these organisms.
⚠️
Click on your ad blocker icon in your browser's toolbar
Select "Pause" or "Disable" for this website
Refresh the page if it doesn't automatically reload
17 min read 
