Growth medium

A growth medium or culture medium is a solid, liquid, or semi-solid designed to support the growth of a population of microorganisms or cells via the process of cell proliferation[1] or small plants like the moss Physcomitrella patens.[2] Different types of media are used for growing different types of cells.[3]

An agar plate – an example of a bacterial growth medium*: Specifically, it is a streak plate; the orange lines and dots are formed by bacterial colonies.

The two major types of growth media are those used for cell culture, which use specific cell types derived from plants or animals, and those used for microbiological culture, which are used for growing microorganisms such as bacteria or fungi. The most common growth media for microorganisms are nutrient broths and agar plates; specialized media are sometimes required for microorganism and cell culture growth.[1] Some organisms, termed fastidious organisms, require specialized environments due to complex nutritional requirements. Viruses, for example, are obligate intracellular parasites and require a growth medium containing living cells.

Types
US Food and Drug Administration scientist tests for Salmonella
A culture of salmonella bacteria

The most common growth media for microorganisms are nutrient broths (liquid nutrient medium) or lysogeny broth medium. Liquid media are often mixed with agar and poured via a sterile media dispenser into Petri dishes to solidify. These agar plates provide a solid medium on which microbes may be cultured. They remain solid, as very few bacteria are able to decompose agar (the exception being some species in the genera: Cytophaga, Flavobacterium, Bacillus, Pseudomonas, and Alcaligenes). Bacteria grown in liquid cultures often form colloidal suspensions.[4][5]

The difference between growth media used for cell culture and those used for microbiological culture is that cells derived from whole organisms and grown in culture often cannot grow without the addition of, for instance, hormones or growth factors which usually occur in vivo.[6] In the case of animal cells, this difficulty is often addressed by the addition of blood serum or a synthetic serum replacement to the medium. In the case of microorganisms, no such limitations exist, as they are often unicellular organisms. One other major difference is that animal cells in culture are often grown on a flat surface to which they attach, and the medium is provided in a liquid form, which covers the cells. In contrast, bacteria such as Escherichia coli may be grown on solid or in liquid media.

An important distinction between growth media types is that of defined versus undefined media.[1] A defined medium will have known quantities of all ingredients. For microorganisms, they consist of providing trace elements and vitamins required by the microbe and especially defined carbon and nitrogen sources. Glucose or glycerol are often used as carbon sources, and ammonium salts or nitrates as inorganic nitrogen sources. An undefined medium has some complex ingredients, such as yeast extract or casein hydrolysate, which consist of a mixture of many chemical species in unknown proportions. Undefined media are sometimes chosen based on price and sometimes by necessity – some microorganisms have never been cultured on defined media.

A good example of a growth medium is the wort used to make beer. The wort contains all the nutrients required for yeast growth, and under anaerobic conditions, alcohol is produced. When the fermentation process is complete, the combination of medium and dormant microbes, now beer, is ready for consumption. The main types are

  • culture media
  • minimal media
  • selective media
  • differential media
  • transport media
  • indicator media

Culture media

Culture media contain all the elements that most bacteria need for growth and are not selective, so they are used for the general cultivation and maintenance of bacteria kept in laboratory culture collections.

Physcomitrella patens plants growing axenically on agar plates (Petri dish, 9 cm diameter)

An undefined medium (also known as a basal or complex medium) contains:

  • a carbon source such as glucose
  • water
  • various salts
  • a source of amino acids and nitrogen (e.g. beef, yeast extract)

This is an undefined medium because the amino-acid source contains a variety of compounds; the exact composition is unknown.

A defined medium (also known as chemically defined medium or synthetic medium) is a medium in which

  • all the chemicals used are known
  • no yeast, animal, or plant tissue is present

Examples of nutrient media:

Minimal media

A defined medium that has just enough ingredients to support growth is called a "minimal medium". The number of ingredients that must be added to a minimal medium varies enormously depending on which microorganism is being grown.[7] Minimal media are those that contain the minimum nutrients possible for colony growth, generally without the presence of amino acids, and are often used by microbiologists and geneticists to grow "wild-type" microorganisms. Minimal media can also be used to select for or against recombinants or exconjugants.

Minimal medium typically contains:

  • a carbon source, which may be a sugar such as glucose, or a less energy-rich source such as succinate
  • various salts, which may vary among bacteria species and growing conditions; these generally provide essential elements such as magnesium, nitrogen, phosphorus, and sulfur to allow the bacteria to synthesize protein and nucleic acids
  • water

Supplementary minimal media are minimal media that also contains a single selected agent, usually an amino acid or a sugar. This supplementation allows for the culturing of specific lines of auxotrophic recombinants.

Selective media
Blood-free, charcoal-based selective medium agar (CSM) for isolation of Campylobacter
Blood agar plates are often used to diagnose infection. On the right is a positive Staphylococcus culture; on the left is a positive Streptococcus culture.

Selective media are used for the growth of only selected microorganisms. For example, if a microorganism is resistant to a certain antibiotic, such as ampicillin or tetracycline, then that antibiotic can be added to the medium to prevent other cells, which do not possess the resistance, from growing. Media lacking an amino acid such as proline in conjunction with E. coli unable to synthesize it were commonly used by geneticists before the emergence of genomics to map bacterial chromosomes.

Selective growth media are also used in cell culture to ensure the survival or proliferation of cells with certain properties, such as antibiotic resistance or the ability to synthesize a certain metabolite. Normally, the presence of a specific gene or an allele of a gene confers upon the cell the ability to grow in the selective medium. In such cases, the gene is termed a marker.

Selective growth media for eukaryotic cells commonly contain neomycin to select cells that have been successfully transfected with a plasmid carrying the neomycin resistance gene as a marker. Gancyclovir is an exception to the rule, as it is used to specifically kill cells that carry its respective marker, the Herpes simplex virus thymidine kinase.

Four types of agar plate demonstrating differential growth depending on bacterial metabolism

Examples of selective media:

Differential media
UTI agar is a chromogenic medium for differentiation of main microorganisms that cause urinary tract infections (UTIs).

Differential or indicator media distinguish one microorganism type from another growing on the same medium.[11] This type of media uses the biochemical characteristics of a microorganism growing in the presence of specific nutrients or indicators (such as neutral red, phenol red, eosin y, or methylene blue) added to the medium to visibly indicate the defining characteristics of a microorganism. These media are used for the detection of microorganisms and by molecular biologists to detect recombinant strains of bacteria.

Examples of differential media:

Transport media

Transport media should fulfill these criteria:

  • Temporary storage of specimens being transported to the laboratory for cultivation
  • Maintain the viability of all organisms in the specimen without altering their concentration
  • Contain only buffers and salt
  • Lack of carbon, nitrogen, and organic growth factors so as to prevent microbial multiplication
  • Transport media used in the isolation of anaerobes must be free of molecular oxygen.

Examples of transport media:

  • Thioglycolate broth is for strict anaerobes.
  • Stuart transport medium[12][13] is a non-nutrient soft agar gel containing a reducing agent to prevent oxidation, and charcoal to neutralize.
  • Certain bacterial inhibitors are used for gonococci, and buffered glycerol saline for enteric bacilli.
  • Venkataraman Ramakrishna (VR) medium is used for V. cholerae.

Enriched media

Enriched media contain the nutrients required to support the growth of a wide variety of organisms, including some of the more fastidious ones. They are commonly used to harvest as many different types of microbes as are present in the specimen. Blood agar is an enriched medium in which nutritionally rich whole blood supplements the basic nutrients. Chocolate agar is enriched with heat-treated blood (40–45 °C or 104–113 °F), which turns brown and gives the medium the color for which it is named.[14]

Physiological relevance

The choice of culture medium might affect the physiological relevance of findings from tissue culture experiments, especially for metabolic studies.[15] In addition, the dependence of a cell line on a metabolic gene was shown to be affected by the media type.[16] When performing a study involving several cell lines, utilizing a uniform culture media for all cell lines might reduce the bias in the generated datasets. Using a growth medium that better represents the physiological levels of nutrients can improve the physiological relevance of in vitro studies and recently such media types, as Plasmax[17] and human plasma-like medium (HPLM),[18] were developed.

See also

References
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  2. Birgit Hadeler; Sirkka Scholz; Ralf Reski (1995). "Gelrite and agar differently influence cytokinin-sensitivity of a moss". Journal of Plant Physiology (146): 369–371.
  3. Ryan KJ, Ray CG, eds. (2004). Sherris Medical Microbiology (4th ed.). McGraw Hill. ISBN 0-8385-8529-9.
  4. Hans Günter Schlegel (1993). General Microbiology. Cambridge University. p. 459. ISBN 978-0-521-43980-0. Retrieved 6 August 2013.
  5. Parija, Shubhash Chandra (1 January 2009). Textbook of Microbiology & Immunology. Elsevier India. p. 45. ISBN 978-81-312-2163-1. Retrieved 6 August 2013.
  6. Cooper, GM (2000). "Tools of Cell Biology". The Cell: A Molecular Approach. Washington, D.C: ASM Press. ISBN 0-87893-106-6.
  7. Catherine A. Ingraham, John L. Ingraham (2000). Introduction to Microbiology.
  8. Corry, Janet E. L.; Curtis, G. D. W.; Baird, Rosamund M., eds. (1995-01-01). "Dichloran rose bengal chloramphenicol (DRBC) agar". Progress in Industrial Microbiology. Elsevier. 34: 303–305. doi:10.1016/s0079-6352(05)80036-0. ISBN 978-0-444-81498-2. Retrieved 2020-04-20.
  9. Islam, Ferzana; Ohga, Shoji (2013-03-12). "Effects of Media Formulation on the Growth and Morphology of Ectomycorrhizae and Their Association with Host Plant". International Scholarly Research Notices. 2013: e317903. doi:10.1155/2013/317903.
  10. Chaitali Bhattacharya; Alok Adholeya. "Showcasing Ectomycorrhizal Culture". bookstore.teri.res.in. Retrieved 2023-02-04.
  11. Washington, JA (1996). "Principles of Diagnosis". In Baron, S; et al. (eds.). Baron's Medical Microbiology (4th ed.). Univ of Texas Medical Branch. ISBN 0-9631172-1-1.
  12. Mitsuhashi, Jun (2002), "Preparation of Media", Invertebrate Tissue Culture Methods, Tokyo: Springer Japan, pp. 25–32, ISBN 978-4-431-70313-6, retrieved 2023-09-07
  13. Smriti, Saifun Nahar (2023-09-07). "Culture media: Definition, Types and Preparation Methods". GreenLeen.Com. Retrieved 2023-09-07.
  14. "Enrichment Culture - an overview". ScienceDirect Topics. Retrieved 2023-09-07.
  15. Lagziel S, GottliebE, Shlomi T (2020). "Mind your media". Nature Metabolism. 2 (12): 1369–1372. doi:10.1038/s42255-020-00299-y. PMID 33046912. S2CID 222319735.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  16. Lagziel S, Lee WD, Shlomi T (2019). "Inferring cancer dependencies on metabolic genes from large-scale genetic screens". BMC Biology. 17 (1): 37. doi:10.1186/s12915-019-0654-4. PMC 6489231. PMID 31039782.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  17. Vande Voorde J, Ackermann T, Pfetzer N, Sumpton D, Mackay G, Kalna G; et al. (2019). "Improving the metabolic fidelity of cancer models with a physiological cell culture medium". Science Advances. 5 (1): eaau7314. Bibcode:2019SciA....5.7314V. doi:10.1126/sciadv.aau7314. PMC 6314821. PMID 30613774.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  18. Cantor JR, Abu-Remaileh M, Kanarek N, Freinkman E, Gao X, Louissaint A; et al. (2017). "Physiologic Medium Rewires Cellular Metabolism and Reveals Uric Acid as an Endogenous Inhibitor of UMP Synthase". Cell. 169 (2): 258–272.e17. doi:10.1016/j.cell.2017.03.023. PMC 5421364. PMID 28388410.{{cite journal}}: CS1 maint: multiple names: authors list (link)
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