1Enterococcosel AgarA selective and differential medium that inhibits the growth of Gram-negative bacteria and distinguishes enterococci based on their ability to grow in the presence of bile and hydrolyze esculin. E. faecalis will form small, black colonies on this medium due to esculin hydrolysis.
2Cornmeal Agar with Tween 80It is used for the identification of Candida species by promoting the formation of chlamydospores, which is a characteristic of Candida albicans.
3Simmons Citrate AgarUsed for citrate utilization testing. E. coli usually can't utilize citrate as a sole carbon source, so no growth or color change would be expected.
4Petragnini MediumAn egg-based medium enriched with additional nutrients to promote the growth of Mycobacterium tuberculosis. Colonies of M. tuberculosis are small, round, buff-colored, and typically take 3-4 weeks to appear.
5Pawlowsky MediumA potato-based medium. Growth of M. tuberculosis may be similar to that seen on the LJ Medium.
6Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
7Phenol Red Mannitol BrothThis is a differential medium, used to determine an organism's ability to ferment mannitol. S. aureus, which can ferment mannitol, will change the medium from red to yellow due to acid production.
8Middlebrook 7H10 AgarA selective medium that contains oleic acid, albumin, dextrose, and catalase. The colonies of M. tuberculosis appear small, rough, and buff to white-colored, taking less time to appear compared to egg-based media.
9RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
10Middlebrook 7H11 AgarThis is a nutrient-rich medium similar to 7H10 but includes additional pyruvate for energy source, promoting more luxurious growth. The colonies of M. tuberculosis appear small, slightly domed, and rough with a butyrous consistency.
11Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
12Dorset MediumAn egg-based medium. M. tuberculosis colonies appear similar to those on Petragnini Medium: small, round, buff-colored, and taking 3-4 weeks to develop.
13MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
14Nutrient Agar (NA)A non-selective medium. E. coli colonies are usually large, circular, grayish-white, moist, and smooth.
15Loeffler MediumA serum-based medium. M. tuberculosis colonies on Loeffler medium are small, dry, wrinkled, and off-white to yellow.
16Azide Dextrose BrothA selective medium inhibiting Gram-negative bacteria, used for the isolation of streptococci and staphylococci from mixed samples. E. faecalis will show a positive growth resulting in a turbid appearance of the broth.
17m-ENDO AgarE. coli colonies appear as green with a metallic sheen, indicating lactose fermentation.
18Nutrient AgarIt is a general-purpose medium. However, E. faecalis grows poorly on nutrient agar, which means it does not proliferate as well on this medium compared to the others listed, indicating a negative or poor growth.
19Liquid Media (such as Nutrient Broth)E. coli exhibits homogenous turbid growth within 12-18 hours. After prolonged incubation, pellicles may form on the surface of the media.
20Potato Dextrose Agar (PDA)Potato Dextrose Agar (PDA) consists of a nutrient-rich substrate, made from dehydrated Potato Infusion and Dextrose, ideal for robust mycological propagation. Agar provides the solidifying medium. Acidification, typically using sterile tartaric acid, adjusts the pH to 3.5 +/- 0.1 to create a more selective environment by inhibiting bacterial proliferation. Additionally, Chloramphenicol is incorporated as an antimicrobial agent to further suppress bacterial contamination, thereby facilitating the selective isolation of fungi.
21Sorbitol-MacConkey agarA variant of MacConkey agar, used in detecting E. coli O157:H7, which does not ferment sorbitol, unlike most strains of E. coli.
22Sauton’s MediumA liquid medium that lacks detergents, which helps in the formation of corded colonies. When M. tuberculosis grows in this medium, it results in turbidity.
23DNase Test AgarS. aureus produces the enzyme DNase which hydrolyses DNA. When S. aureus grows on this medium, the DNA is broken down, which can be visualised using a hydrochloric acid (HCl) solution: clear zones around the colonies indicate DNA breakdown.
24Baird-Parker Agar (BPA)his is a selective medium for the isolation of Staphylococcus species. It has lithium chloride and glycine to inhibit the growth of Gram-negative bacteria and most Gram-positive bacteria except Staphylococcus. Egg yolk emulsion is added to detect lecithinase production and tellurite reduction. S. aureus colonies on BPA are black due to reduction of tellurite, and they exhibit a clear zone due to lecithinase activity on egg yolk.
25Proskauer and Beck’s MediumA liquid medium. The growth of M. tuberculosis causes turbidity.
26Middlebrook 7H9 BrothThis is a liquid medium that contains glycerol and Tween 80, which prevent clumping of mycobacteria. The growth of M. tuberculosis results in turbidity.
27Tryptic Soy Agar (TSA)A general purpose medium. E. coli colonies are medium to large, with a shiny moist appearance.
28Dubos’ MediumA liquid medium that contains a mixture of salts, fatty acids, and polysorbate. When M. tuberculosis grows in this medium, it causes the medium to become turbid.
29Urea Agar/BrothE. coli is typically urease negative, so no color change would be expected in this medium.
30Triple Sugar Iron (TSI) AgarE. coli typically produces an acid butt, acid slant, and gas, with no H2S production, indicating it ferments lactose, sucrose, and glucose.
31Bile Esculin Agar (BEA)A selective and differential medium that differentiates group D Streptococci and Enterococci based on the ability to hydrolyze esculin in the presence of bile. E. faecalis hydrolyzes esculin, leading to the formation of a dark brown or black precipita
32Brilliant Green Agar (BGA)A selective medium that is used to isolate Salmonella species, but E. coli can grow on it, albeit not as well.
33Blood AgarA differential medium used to identify bacteria based on their hemolytic properties. E. faecalis typically shows gamma-hemolysis on this medium, i.e., no hemolysis or change in the color of the medium.
34Todd-Hewitt BrothA liquid enrichment medium used for the cultivation of fastidious organisms such as streptococci and enterococci. E. faecalis will lead to a turbid broth due to microbial growth.
35Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
36Mannitol Salt Agar (MSA), or Chapman AgarThis is a selective and differential medium. The high concentration of NaCl (~7.5%) selects for halophiles, organisms that can tolerate high salt concentrations, thereby favouring the growth of Staphylococcus species. Mannitol is the differential component: S. aureus ferments mannitol, lowering the pH of the medium, which results in a color change of the pH indicator from red to yellow. Thus, growth of S. aureus is indicated by yellow colonies.
37Nickerson’s Medium or Bismuth Sulfite Glucose Glycine Yeast (BSGG)This medium is used to stimulate the production of germ tubes, a characteristic of Candida albicans.
38Sf1Ep mediumCulturing Treponema pallidum, the bacteria that causes syphilis, in vitro is a challenge. T. pallidum is not routinely cultured in the laboratory for diagnostic purposes, in part because it cannot be grown on artificial media. However, a breakthrough in culturing T. pallidum was reported in 2018 when researchers managed to grow the bacterium in a rabbit epithelial cell line (Sf1Ep) using a medium called 'Sf1Ep medium'. It's not used for routine diagnostic purposes, but for research only. The diagnosis involves direct microscopic examination, serologic tests, molecular tests and histopathology.
39Blood Agar (BA)This is a nutrient-rich, differential medium that supports the growth of many organisms. S. aureus forms colonies that are round, smooth, and golden-yellow. This bacterium typically demonstrates β-hemolysis, which is complete lysis of red blood cells, resulting in a clear zone around the colonies. This hemolysis is due to the production of hemolysins by S. aureus.
40CHROMagar CandidaThis differential medium allows for the isolation and identification of Candida species based on colony color. Candida albicans usually forms green colonies on this medium.
41Sabouraud Dextrose Agar (SDA)It is composed of peptone, dextrose (glucose), and agar. The high dextrose concentration promotes fungal growth, while the acidic pH inhibits bacterial growth.
42BACTECThis is not a traditional medium but a system for detecting the growth of M. tuberculosis by monitoring the release of C14O2 from C14 palmitic acid, which the bacteria metabolize. An increase in radioactive counts in the BACTEC instrument indicates the growth of bacteria.
43Tarshis MediumA blood-based medium that can promote the growth of M. tuberculosis. The colonies appear similar to those on the LJ Medium.
44Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
45Violet Red Bile Agar (VRBA)E. coli colonies are red (pink to red) and may show bluish fluorescence under UV light.
1Sf1Ep mediumCulturing Treponema pallidum, the bacteria that causes syphilis, in vitro is a challenge. T. pallidum is not routinely cultured in the laboratory for diagnostic purposes, in part because it cannot be grown on artificial media. However, a breakthrough in culturing T. pallidum was reported in 2018 when researchers managed to grow the bacterium in a rabbit epithelial cell line (Sf1Ep) using a medium called 'Sf1Ep medium'. It's not used for routine diagnostic purposes, but for research only. The diagnosis involves direct microscopic examination, serologic tests, molecular tests and histopathology.
2Phenol Red Mannitol BrothThis is a differential medium, used to determine an organism's ability to ferment mannitol. S. aureus, which can ferment mannitol, will change the medium from red to yellow due to acid production.
3DNase Test AgarS. aureus produces the enzyme DNase which hydrolyses DNA. When S. aureus grows on this medium, the DNA is broken down, which can be visualised using a hydrochloric acid (HCl) solution: clear zones around the colonies indicate DNA breakdown.
4Mannitol Salt Agar (MSA), or Chapman AgarThis is a selective and differential medium. The high concentration of NaCl (~7.5%) selects for halophiles, organisms that can tolerate high salt concentrations, thereby favouring the growth of Staphylococcus species. Mannitol is the differential component: S. aureus ferments mannitol, lowering the pH of the medium, which results in a color change of the pH indicator from red to yellow. Thus, growth of S. aureus is indicated by yellow colonies.
5Blood Agar (BA)This is a nutrient-rich, differential medium that supports the growth of many organisms. S. aureus forms colonies that are round, smooth, and golden-yellow. This bacterium typically demonstrates β-hemolysis, which is complete lysis of red blood cells, resulting in a clear zone around the colonies. This hemolysis is due to the production of hemolysins by S. aureus.
6BACTECThis is not a traditional medium but a system for detecting the growth of M. tuberculosis by monitoring the release of C14O2 from C14 palmitic acid, which the bacteria metabolize. An increase in radioactive counts in the BACTEC instrument indicates the growth of bacteria.
7Proskauer and Beck’s MediumA liquid medium. The growth of M. tuberculosis causes turbidity.
8Middlebrook 7H9 BrothThis is a liquid medium that contains glycerol and Tween 80, which prevent clumping of mycobacteria. The growth of M. tuberculosis results in turbidity.
9Dubos’ MediumA liquid medium that contains a mixture of salts, fatty acids, and polysorbate. When M. tuberculosis grows in this medium, it causes the medium to become turbid.
10Pawlowsky MediumA potato-based medium. Growth of M. tuberculosis may be similar to that seen on the LJ Medium.
11Loeffler MediumA serum-based medium. M. tuberculosis colonies on Loeffler medium are small, dry, wrinkled, and off-white to yellow.
12Tarshis MediumA blood-based medium that can promote the growth of M. tuberculosis. The colonies appear similar to those on the LJ Medium.
13Dorset MediumAn egg-based medium. M. tuberculosis colonies appear similar to those on Petragnini Medium: small, round, buff-colored, and taking 3-4 weeks to develop.
14Middlebrook 7H11 AgarThis is a nutrient-rich medium similar to 7H10 but includes additional pyruvate for energy source, promoting more luxurious growth. The colonies of M. tuberculosis appear small, slightly domed, and rough with a butyrous consistency.
15Middlebrook 7H10 AgarA selective medium that contains oleic acid, albumin, dextrose, and catalase. The colonies of M. tuberculosis appear small, rough, and buff to white-colored, taking less time to appear compared to egg-based media.
16Petragnini MediumAn egg-based medium enriched with additional nutrients to promote the growth of Mycobacterium tuberculosis. Colonies of M. tuberculosis are small, round, buff-colored, and typically take 3-4 weeks to appear.
17Liquid Media (such as Nutrient Broth)E. coli exhibits homogenous turbid growth within 12-18 hours. After prolonged incubation, pellicles may form on the surface of the media.
18Brilliant Green Agar (BGA)A selective medium that is used to isolate Salmonella species, but E. coli can grow on it, albeit not as well.
19Sorbitol-MacConkey agarA variant of MacConkey agar, used in detecting E. coli O157:H7, which does not ferment sorbitol, unlike most strains of E. coli.
20Simmons Citrate AgarUsed for citrate utilization testing. E. coli usually can't utilize citrate as a sole carbon source, so no growth or color change would be expected.
21Tryptic Soy Agar (TSA)A general purpose medium. E. coli colonies are medium to large, with a shiny moist appearance.
22Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
23m-ENDO AgarE. coli colonies appear as green with a metallic sheen, indicating lactose fermentation.
24Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
25Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
26MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
27Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
28Nutrient Agar (NA)A non-selective medium. E. coli colonies are usually large, circular, grayish-white, moist, and smooth.
29Cornmeal Agar with Tween 80It is used for the identification of Candida species by promoting the formation of chlamydospores, which is a characteristic of Candida albicans.
30RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
31Potato Dextrose Agar (PDA)Potato Dextrose Agar (PDA) consists of a nutrient-rich substrate, made from dehydrated Potato Infusion and Dextrose, ideal for robust mycological propagation. Agar provides the solidifying medium. Acidification, typically using sterile tartaric acid, adjusts the pH to 3.5 +/- 0.1 to create a more selective environment by inhibiting bacterial proliferation. Additionally, Chloramphenicol is incorporated as an antimicrobial agent to further suppress bacterial contamination, thereby facilitating the selective isolation of fungi.
32Sabouraud Dextrose Agar (SDA)It is composed of peptone, dextrose (glucose), and agar. The high dextrose concentration promotes fungal growth, while the acidic pH inhibits bacterial growth.
33Nutrient AgarIt is a general-purpose medium. However, E. faecalis grows poorly on nutrient agar, which means it does not proliferate as well on this medium compared to the others listed, indicating a negative or poor growth.
34Azide Dextrose BrothA selective medium inhibiting Gram-negative bacteria, used for the isolation of streptococci and staphylococci from mixed samples. E. faecalis will show a positive growth resulting in a turbid appearance of the broth.
35Todd-Hewitt BrothA liquid enrichment medium used for the cultivation of fastidious organisms such as streptococci and enterococci. E. faecalis will lead to a turbid broth due to microbial growth.
36Enterococcosel AgarA selective and differential medium that inhibits the growth of Gram-negative bacteria and distinguishes enterococci based on their ability to grow in the presence of bile and hydrolyze esculin. E. faecalis will form small, black colonies on this medium due to esculin hydrolysis.
37Brain-Heart Infusion (BHI) Broth or AgarThis is a nutrient-rich medium that supports the growth of a variety of fastidious organisms, including E. faecalis. The typical phenotype of E. faecalis on BHI is small, round, and white colonies.
38Tryptic Soy Broth or Agar (TSB/TSA)A general-purpose medium that supports the growth of a broad spectrum of bacteria. E. faecalis on TSA will typically form small, round, and white colonies, indicating a positive growth.
1DNase Test AgarS. aureus produces the enzyme DNase which hydrolyses DNA. When S. aureus grows on this medium, the DNA is broken down, which can be visualised using a hydrochloric acid (HCl) solution: clear zones around the colonies indicate DNA breakdown.
2Blood Agar (BA)This is a nutrient-rich, differential medium that supports the growth of many organisms. S. aureus forms colonies that are round, smooth, and golden-yellow. This bacterium typically demonstrates β-hemolysis, which is complete lysis of red blood cells, resulting in a clear zone around the colonies. This hemolysis is due to the production of hemolysins by S. aureus.
3Sauton’s MediumA liquid medium that lacks detergents, which helps in the formation of corded colonies. When M. tuberculosis grows in this medium, it results in turbidity.
4BACTECThis is not a traditional medium but a system for detecting the growth of M. tuberculosis by monitoring the release of C14O2 from C14 palmitic acid, which the bacteria metabolize. An increase in radioactive counts in the BACTEC instrument indicates the growth of bacteria.
5Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
6Proskauer and Beck’s MediumA liquid medium. The growth of M. tuberculosis causes turbidity.
7Pawlowsky MediumA potato-based medium. Growth of M. tuberculosis may be similar to that seen on the LJ Medium.
8Dorset MediumAn egg-based medium. M. tuberculosis colonies appear similar to those on Petragnini Medium: small, round, buff-colored, and taking 3-4 weeks to develop.
9Middlebrook 7H11 AgarThis is a nutrient-rich medium similar to 7H10 but includes additional pyruvate for energy source, promoting more luxurious growth. The colonies of M. tuberculosis appear small, slightly domed, and rough with a butyrous consistency.
10Middlebrook 7H10 AgarA selective medium that contains oleic acid, albumin, dextrose, and catalase. The colonies of M. tuberculosis appear small, rough, and buff to white-colored, taking less time to appear compared to egg-based media.
11Petragnini MediumAn egg-based medium enriched with additional nutrients to promote the growth of Mycobacterium tuberculosis. Colonies of M. tuberculosis are small, round, buff-colored, and typically take 3-4 weeks to appear.
12Liquid Media (such as Nutrient Broth)E. coli exhibits homogenous turbid growth within 12-18 hours. After prolonged incubation, pellicles may form on the surface of the media.
13Brilliant Green Agar (BGA)A selective medium that is used to isolate Salmonella species, but E. coli can grow on it, albeit not as well.
14Sorbitol-MacConkey agarA variant of MacConkey agar, used in detecting E. coli O157:H7, which does not ferment sorbitol, unlike most strains of E. coli.
15Urea Agar/BrothE. coli is typically urease negative, so no color change would be expected in this medium.
16Triple Sugar Iron (TSI) AgarE. coli typically produces an acid butt, acid slant, and gas, with no H2S production, indicating it ferments lactose, sucrose, and glucose.
17Simmons Citrate AgarUsed for citrate utilization testing. E. coli usually can't utilize citrate as a sole carbon source, so no growth or color change would be expected.
18Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
19Violet Red Bile Agar (VRBA)E. coli colonies are red (pink to red) and may show bluish fluorescence under UV light.
20m-ENDO AgarE. coli colonies appear as green with a metallic sheen, indicating lactose fermentation.
21Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
22Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
23MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
24Nickerson’s Medium or Bismuth Sulfite Glucose Glycine Yeast (BSGG)This medium is used to stimulate the production of germ tubes, a characteristic of Candida albicans.
25Cornmeal Agar with Tween 80It is used for the identification of Candida species by promoting the formation of chlamydospores, which is a characteristic of Candida albicans.
26CHROMagar CandidaThis differential medium allows for the isolation and identification of Candida species based on colony color. Candida albicans usually forms green colonies on this medium.
27RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
28Potato Dextrose Agar (PDA)Potato Dextrose Agar (PDA) consists of a nutrient-rich substrate, made from dehydrated Potato Infusion and Dextrose, ideal for robust mycological propagation. Agar provides the solidifying medium. Acidification, typically using sterile tartaric acid, adjusts the pH to 3.5 +/- 0.1 to create a more selective environment by inhibiting bacterial proliferation. Additionally, Chloramphenicol is incorporated as an antimicrobial agent to further suppress bacterial contamination, thereby facilitating the selective isolation of fungi.
29Nutrient AgarIt is a general-purpose medium. However, E. faecalis grows poorly on nutrient agar, which means it does not proliferate as well on this medium compared to the others listed, indicating a negative or poor growth.
30Blood AgarA differential medium used to identify bacteria based on their hemolytic properties. E. faecalis typically shows gamma-hemolysis on this medium, i.e., no hemolysis or change in the color of the medium.
31Todd-Hewitt BrothA liquid enrichment medium used for the cultivation of fastidious organisms such as streptococci and enterococci. E. faecalis will lead to a turbid broth due to microbial growth.
32Enterococcosel AgarA selective and differential medium that inhibits the growth of Gram-negative bacteria and distinguishes enterococci based on their ability to grow in the presence of bile and hydrolyze esculin. E. faecalis will form small, black colonies on this medium due to esculin hydrolysis.
33Bile Esculin Agar (BEA)A selective and differential medium that differentiates group D Streptococci and Enterococci based on the ability to hydrolyze esculin in the presence of bile. E. faecalis hydrolyzes esculin, leading to the formation of a dark brown or black precipita
34Brain-Heart Infusion (BHI) Broth or AgarThis is a nutrient-rich medium that supports the growth of a variety of fastidious organisms, including E. faecalis. The typical phenotype of E. faecalis on BHI is small, round, and white colonies.
1Sf1Ep mediumCulturing Treponema pallidum, the bacteria that causes syphilis, in vitro is a challenge. T. pallidum is not routinely cultured in the laboratory for diagnostic purposes, in part because it cannot be grown on artificial media. However, a breakthrough in culturing T. pallidum was reported in 2018 when researchers managed to grow the bacterium in a rabbit epithelial cell line (Sf1Ep) using a medium called 'Sf1Ep medium'. It's not used for routine diagnostic purposes, but for research only. The diagnosis involves direct microscopic examination, serologic tests, molecular tests and histopathology.
2Baird-Parker Agar (BPA)his is a selective medium for the isolation of Staphylococcus species. It has lithium chloride and glycine to inhibit the growth of Gram-negative bacteria and most Gram-positive bacteria except Staphylococcus. Egg yolk emulsion is added to detect lecithinase production and tellurite reduction. S. aureus colonies on BPA are black due to reduction of tellurite, and they exhibit a clear zone due to lecithinase activity on egg yolk.
3Phenol Red Mannitol BrothThis is a differential medium, used to determine an organism's ability to ferment mannitol. S. aureus, which can ferment mannitol, will change the medium from red to yellow due to acid production.
4Mannitol Salt Agar (MSA), or Chapman AgarThis is a selective and differential medium. The high concentration of NaCl (~7.5%) selects for halophiles, organisms that can tolerate high salt concentrations, thereby favouring the growth of Staphylococcus species. Mannitol is the differential component: S. aureus ferments mannitol, lowering the pH of the medium, which results in a color change of the pH indicator from red to yellow. Thus, growth of S. aureus is indicated by yellow colonies.
5Blood Agar (BA)This is a nutrient-rich, differential medium that supports the growth of many organisms. S. aureus forms colonies that are round, smooth, and golden-yellow. This bacterium typically demonstrates β-hemolysis, which is complete lysis of red blood cells, resulting in a clear zone around the colonies. This hemolysis is due to the production of hemolysins by S. aureus.
6Sauton’s MediumA liquid medium that lacks detergents, which helps in the formation of corded colonies. When M. tuberculosis grows in this medium, it results in turbidity.
7BACTECThis is not a traditional medium but a system for detecting the growth of M. tuberculosis by monitoring the release of C14O2 from C14 palmitic acid, which the bacteria metabolize. An increase in radioactive counts in the BACTEC instrument indicates the growth of bacteria.
8Proskauer and Beck’s MediumA liquid medium. The growth of M. tuberculosis causes turbidity.
9Middlebrook 7H9 BrothThis is a liquid medium that contains glycerol and Tween 80, which prevent clumping of mycobacteria. The growth of M. tuberculosis results in turbidity.
10Dubos’ MediumA liquid medium that contains a mixture of salts, fatty acids, and polysorbate. When M. tuberculosis grows in this medium, it causes the medium to become turbid.
11Pawlowsky MediumA potato-based medium. Growth of M. tuberculosis may be similar to that seen on the LJ Medium.
12Loeffler MediumA serum-based medium. M. tuberculosis colonies on Loeffler medium are small, dry, wrinkled, and off-white to yellow.
13Tarshis MediumA blood-based medium that can promote the growth of M. tuberculosis. The colonies appear similar to those on the LJ Medium.
14Dorset MediumAn egg-based medium. M. tuberculosis colonies appear similar to those on Petragnini Medium: small, round, buff-colored, and taking 3-4 weeks to develop.
15Middlebrook 7H11 AgarThis is a nutrient-rich medium similar to 7H10 but includes additional pyruvate for energy source, promoting more luxurious growth. The colonies of M. tuberculosis appear small, slightly domed, and rough with a butyrous consistency.
16Middlebrook 7H10 AgarA selective medium that contains oleic acid, albumin, dextrose, and catalase. The colonies of M. tuberculosis appear small, rough, and buff to white-colored, taking less time to appear compared to egg-based media.
17Petragnini MediumAn egg-based medium enriched with additional nutrients to promote the growth of Mycobacterium tuberculosis. Colonies of M. tuberculosis are small, round, buff-colored, and typically take 3-4 weeks to appear.
18Urea Agar/BrothE. coli is typically urease negative, so no color change would be expected in this medium.
19Simmons Citrate AgarUsed for citrate utilization testing. E. coli usually can't utilize citrate as a sole carbon source, so no growth or color change would be expected.
20Tryptic Soy Agar (TSA)A general purpose medium. E. coli colonies are medium to large, with a shiny moist appearance.
21Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
22Violet Red Bile Agar (VRBA)E. coli colonies are red (pink to red) and may show bluish fluorescence under UV light.
23Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
24Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
25MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
26Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
27Nutrient Agar (NA)A non-selective medium. E. coli colonies are usually large, circular, grayish-white, moist, and smooth.
28Nickerson’s Medium or Bismuth Sulfite Glucose Glycine Yeast (BSGG)This medium is used to stimulate the production of germ tubes, a characteristic of Candida albicans.
29Cornmeal Agar with Tween 80It is used for the identification of Candida species by promoting the formation of chlamydospores, which is a characteristic of Candida albicans.
30CHROMagar CandidaThis differential medium allows for the isolation and identification of Candida species based on colony color. Candida albicans usually forms green colonies on this medium.
31RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
32Potato Dextrose Agar (PDA)Potato Dextrose Agar (PDA) consists of a nutrient-rich substrate, made from dehydrated Potato Infusion and Dextrose, ideal for robust mycological propagation. Agar provides the solidifying medium. Acidification, typically using sterile tartaric acid, adjusts the pH to 3.5 +/- 0.1 to create a more selective environment by inhibiting bacterial proliferation. Additionally, Chloramphenicol is incorporated as an antimicrobial agent to further suppress bacterial contamination, thereby facilitating the selective isolation of fungi.
33Sabouraud Dextrose Agar (SDA)It is composed of peptone, dextrose (glucose), and agar. The high dextrose concentration promotes fungal growth, while the acidic pH inhibits bacterial growth.
34Azide Dextrose BrothA selective medium inhibiting Gram-negative bacteria, used for the isolation of streptococci and staphylococci from mixed samples. E. faecalis will show a positive growth resulting in a turbid appearance of the broth.
35Enterococcosel AgarA selective and differential medium that inhibits the growth of Gram-negative bacteria and distinguishes enterococci based on their ability to grow in the presence of bile and hydrolyze esculin. E. faecalis will form small, black colonies on this medium due to esculin hydrolysis.
36Brain-Heart Infusion (BHI) Broth or AgarThis is a nutrient-rich medium that supports the growth of a variety of fastidious organisms, including E. faecalis. The typical phenotype of E. faecalis on BHI is small, round, and white colonies.
37Tryptic Soy Broth or Agar (TSB/TSA)A general-purpose medium that supports the growth of a broad spectrum of bacteria. E. faecalis on TSA will typically form small, round, and white colonies, indicating a positive growth.
1Sf1Ep mediumCulturing Treponema pallidum, the bacteria that causes syphilis, in vitro is a challenge. T. pallidum is not routinely cultured in the laboratory for diagnostic purposes, in part because it cannot be grown on artificial media. However, a breakthrough in culturing T. pallidum was reported in 2018 when researchers managed to grow the bacterium in a rabbit epithelial cell line (Sf1Ep) using a medium called 'Sf1Ep medium'. It's not used for routine diagnostic purposes, but for research only. The diagnosis involves direct microscopic examination, serologic tests, molecular tests and histopathology.
2Baird-Parker Agar (BPA)his is a selective medium for the isolation of Staphylococcus species. It has lithium chloride and glycine to inhibit the growth of Gram-negative bacteria and most Gram-positive bacteria except Staphylococcus. Egg yolk emulsion is added to detect lecithinase production and tellurite reduction. S. aureus colonies on BPA are black due to reduction of tellurite, and they exhibit a clear zone due to lecithinase activity on egg yolk.
3Phenol Red Mannitol BrothThis is a differential medium, used to determine an organism's ability to ferment mannitol. S. aureus, which can ferment mannitol, will change the medium from red to yellow due to acid production.
4Blood Agar (BA)This is a nutrient-rich, differential medium that supports the growth of many organisms. S. aureus forms colonies that are round, smooth, and golden-yellow. This bacterium typically demonstrates β-hemolysis, which is complete lysis of red blood cells, resulting in a clear zone around the colonies. This hemolysis is due to the production of hemolysins by S. aureus.
5Sauton’s MediumA liquid medium that lacks detergents, which helps in the formation of corded colonies. When M. tuberculosis grows in this medium, it results in turbidity.
6BACTECThis is not a traditional medium but a system for detecting the growth of M. tuberculosis by monitoring the release of C14O2 from C14 palmitic acid, which the bacteria metabolize. An increase in radioactive counts in the BACTEC instrument indicates the growth of bacteria.
7Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
8Middlebrook 7H9 BrothThis is a liquid medium that contains glycerol and Tween 80, which prevent clumping of mycobacteria. The growth of M. tuberculosis results in turbidity.
9Pawlowsky MediumA potato-based medium. Growth of M. tuberculosis may be similar to that seen on the LJ Medium.
10Loeffler MediumA serum-based medium. M. tuberculosis colonies on Loeffler medium are small, dry, wrinkled, and off-white to yellow.
11Tarshis MediumA blood-based medium that can promote the growth of M. tuberculosis. The colonies appear similar to those on the LJ Medium.
12Dorset MediumAn egg-based medium. M. tuberculosis colonies appear similar to those on Petragnini Medium: small, round, buff-colored, and taking 3-4 weeks to develop.
13Middlebrook 7H11 AgarThis is a nutrient-rich medium similar to 7H10 but includes additional pyruvate for energy source, promoting more luxurious growth. The colonies of M. tuberculosis appear small, slightly domed, and rough with a butyrous consistency.
14Middlebrook 7H10 AgarA selective medium that contains oleic acid, albumin, dextrose, and catalase. The colonies of M. tuberculosis appear small, rough, and buff to white-colored, taking less time to appear compared to egg-based media.
15Petragnini MediumAn egg-based medium enriched with additional nutrients to promote the growth of Mycobacterium tuberculosis. Colonies of M. tuberculosis are small, round, buff-colored, and typically take 3-4 weeks to appear.
16Liquid Media (such as Nutrient Broth)E. coli exhibits homogenous turbid growth within 12-18 hours. After prolonged incubation, pellicles may form on the surface of the media.
17Brilliant Green Agar (BGA)A selective medium that is used to isolate Salmonella species, but E. coli can grow on it, albeit not as well.
18Sorbitol-MacConkey agarA variant of MacConkey agar, used in detecting E. coli O157:H7, which does not ferment sorbitol, unlike most strains of E. coli.
19Urea Agar/BrothE. coli is typically urease negative, so no color change would be expected in this medium.
20Triple Sugar Iron (TSI) AgarE. coli typically produces an acid butt, acid slant, and gas, with no H2S production, indicating it ferments lactose, sucrose, and glucose.
21Simmons Citrate AgarUsed for citrate utilization testing. E. coli usually can't utilize citrate as a sole carbon source, so no growth or color change would be expected.
22Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
23Violet Red Bile Agar (VRBA)E. coli colonies are red (pink to red) and may show bluish fluorescence under UV light.
24Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
25Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
26MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
27Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
28Nutrient Agar (NA)A non-selective medium. E. coli colonies are usually large, circular, grayish-white, moist, and smooth.
29Cornmeal Agar with Tween 80It is used for the identification of Candida species by promoting the formation of chlamydospores, which is a characteristic of Candida albicans.
30CHROMagar CandidaThis differential medium allows for the isolation and identification of Candida species based on colony color. Candida albicans usually forms green colonies on this medium.
31RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
32Potato Dextrose Agar (PDA)Potato Dextrose Agar (PDA) consists of a nutrient-rich substrate, made from dehydrated Potato Infusion and Dextrose, ideal for robust mycological propagation. Agar provides the solidifying medium. Acidification, typically using sterile tartaric acid, adjusts the pH to 3.5 +/- 0.1 to create a more selective environment by inhibiting bacterial proliferation. Additionally, Chloramphenicol is incorporated as an antimicrobial agent to further suppress bacterial contamination, thereby facilitating the selective isolation of fungi.
33Sabouraud Dextrose Agar (SDA)It is composed of peptone, dextrose (glucose), and agar. The high dextrose concentration promotes fungal growth, while the acidic pH inhibits bacterial growth.
34Nutrient AgarIt is a general-purpose medium. However, E. faecalis grows poorly on nutrient agar, which means it does not proliferate as well on this medium compared to the others listed, indicating a negative or poor growth.
35Blood AgarA differential medium used to identify bacteria based on their hemolytic properties. E. faecalis typically shows gamma-hemolysis on this medium, i.e., no hemolysis or change in the color of the medium.
36Azide Dextrose BrothA selective medium inhibiting Gram-negative bacteria, used for the isolation of streptococci and staphylococci from mixed samples. E. faecalis will show a positive growth resulting in a turbid appearance of the broth.
37Todd-Hewitt BrothA liquid enrichment medium used for the cultivation of fastidious organisms such as streptococci and enterococci. E. faecalis will lead to a turbid broth due to microbial growth.
38Enterococcosel AgarA selective and differential medium that inhibits the growth of Gram-negative bacteria and distinguishes enterococci based on their ability to grow in the presence of bile and hydrolyze esculin. E. faecalis will form small, black colonies on this medium due to esculin hydrolysis.
39Bile Esculin Agar (BEA)A selective and differential medium that differentiates group D Streptococci and Enterococci based on the ability to hydrolyze esculin in the presence of bile. E. faecalis hydrolyzes esculin, leading to the formation of a dark brown or black precipita
40Brain-Heart Infusion (BHI) Broth or AgarThis is a nutrient-rich medium that supports the growth of a variety of fastidious organisms, including E. faecalis. The typical phenotype of E. faecalis on BHI is small, round, and white colonies.
1Sf1Ep mediumCulturing Treponema pallidum, the bacteria that causes syphilis, in vitro is a challenge. T. pallidum is not routinely cultured in the laboratory for diagnostic purposes, in part because it cannot be grown on artificial media. However, a breakthrough in culturing T. pallidum was reported in 2018 when researchers managed to grow the bacterium in a rabbit epithelial cell line (Sf1Ep) using a medium called 'Sf1Ep medium'. It's not used for routine diagnostic purposes, but for research only. The diagnosis involves direct microscopic examination, serologic tests, molecular tests and histopathology.
2Baird-Parker Agar (BPA)his is a selective medium for the isolation of Staphylococcus species. It has lithium chloride and glycine to inhibit the growth of Gram-negative bacteria and most Gram-positive bacteria except Staphylococcus. Egg yolk emulsion is added to detect lecithinase production and tellurite reduction. S. aureus colonies on BPA are black due to reduction of tellurite, and they exhibit a clear zone due to lecithinase activity on egg yolk.
3Phenol Red Mannitol BrothThis is a differential medium, used to determine an organism's ability to ferment mannitol. S. aureus, which can ferment mannitol, will change the medium from red to yellow due to acid production.
4DNase Test AgarS. aureus produces the enzyme DNase which hydrolyses DNA. When S. aureus grows on this medium, the DNA is broken down, which can be visualised using a hydrochloric acid (HCl) solution: clear zones around the colonies indicate DNA breakdown.
5Sauton’s MediumA liquid medium that lacks detergents, which helps in the formation of corded colonies. When M. tuberculosis grows in this medium, it results in turbidity.
6BACTECThis is not a traditional medium but a system for detecting the growth of M. tuberculosis by monitoring the release of C14O2 from C14 palmitic acid, which the bacteria metabolize. An increase in radioactive counts in the BACTEC instrument indicates the growth of bacteria.
7Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
8Proskauer and Beck’s MediumA liquid medium. The growth of M. tuberculosis causes turbidity.
9Pawlowsky MediumA potato-based medium. Growth of M. tuberculosis may be similar to that seen on the LJ Medium.
10Dorset MediumAn egg-based medium. M. tuberculosis colonies appear similar to those on Petragnini Medium: small, round, buff-colored, and taking 3-4 weeks to develop.
11Middlebrook 7H11 AgarThis is a nutrient-rich medium similar to 7H10 but includes additional pyruvate for energy source, promoting more luxurious growth. The colonies of M. tuberculosis appear small, slightly domed, and rough with a butyrous consistency.
12Middlebrook 7H10 AgarA selective medium that contains oleic acid, albumin, dextrose, and catalase. The colonies of M. tuberculosis appear small, rough, and buff to white-colored, taking less time to appear compared to egg-based media.
13Petragnini MediumAn egg-based medium enriched with additional nutrients to promote the growth of Mycobacterium tuberculosis. Colonies of M. tuberculosis are small, round, buff-colored, and typically take 3-4 weeks to appear.
14Liquid Media (such as Nutrient Broth)E. coli exhibits homogenous turbid growth within 12-18 hours. After prolonged incubation, pellicles may form on the surface of the media.
15Brilliant Green Agar (BGA)A selective medium that is used to isolate Salmonella species, but E. coli can grow on it, albeit not as well.
16Sorbitol-MacConkey agarA variant of MacConkey agar, used in detecting E. coli O157:H7, which does not ferment sorbitol, unlike most strains of E. coli.
17Urea Agar/BrothE. coli is typically urease negative, so no color change would be expected in this medium.
18Triple Sugar Iron (TSI) AgarE. coli typically produces an acid butt, acid slant, and gas, with no H2S production, indicating it ferments lactose, sucrose, and glucose.
19Simmons Citrate AgarUsed for citrate utilization testing. E. coli usually can't utilize citrate as a sole carbon source, so no growth or color change would be expected.
20Tryptic Soy Agar (TSA)A general purpose medium. E. coli colonies are medium to large, with a shiny moist appearance.
21Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
22Violet Red Bile Agar (VRBA)E. coli colonies are red (pink to red) and may show bluish fluorescence under UV light.
23Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
24Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
25MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
26Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
27Nutrient Agar (NA)A non-selective medium. E. coli colonies are usually large, circular, grayish-white, moist, and smooth.
28Cornmeal Agar with Tween 80It is used for the identification of Candida species by promoting the formation of chlamydospores, which is a characteristic of Candida albicans.
29CHROMagar CandidaThis differential medium allows for the isolation and identification of Candida species based on colony color. Candida albicans usually forms green colonies on this medium.
30RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
31Potato Dextrose Agar (PDA)Potato Dextrose Agar (PDA) consists of a nutrient-rich substrate, made from dehydrated Potato Infusion and Dextrose, ideal for robust mycological propagation. Agar provides the solidifying medium. Acidification, typically using sterile tartaric acid, adjusts the pH to 3.5 +/- 0.1 to create a more selective environment by inhibiting bacterial proliferation. Additionally, Chloramphenicol is incorporated as an antimicrobial agent to further suppress bacterial contamination, thereby facilitating the selective isolation of fungi.
32Sabouraud Dextrose Agar (SDA)It is composed of peptone, dextrose (glucose), and agar. The high dextrose concentration promotes fungal growth, while the acidic pH inhibits bacterial growth.
33Nutrient AgarIt is a general-purpose medium. However, E. faecalis grows poorly on nutrient agar, which means it does not proliferate as well on this medium compared to the others listed, indicating a negative or poor growth.
34Blood AgarA differential medium used to identify bacteria based on their hemolytic properties. E. faecalis typically shows gamma-hemolysis on this medium, i.e., no hemolysis or change in the color of the medium.
35Todd-Hewitt BrothA liquid enrichment medium used for the cultivation of fastidious organisms such as streptococci and enterococci. E. faecalis will lead to a turbid broth due to microbial growth.
36Enterococcosel AgarA selective and differential medium that inhibits the growth of Gram-negative bacteria and distinguishes enterococci based on their ability to grow in the presence of bile and hydrolyze esculin. E. faecalis will form small, black colonies on this medium due to esculin hydrolysis.
37Bile Esculin Agar (BEA)A selective and differential medium that differentiates group D Streptococci and Enterococci based on the ability to hydrolyze esculin in the presence of bile. E. faecalis hydrolyzes esculin, leading to the formation of a dark brown or black precipita
38Brain-Heart Infusion (BHI) Broth or AgarThis is a nutrient-rich medium that supports the growth of a variety of fastidious organisms, including E. faecalis. The typical phenotype of E. faecalis on BHI is small, round, and white colonies.
1Sf1Ep mediumCulturing Treponema pallidum, the bacteria that causes syphilis, in vitro is a challenge. T. pallidum is not routinely cultured in the laboratory for diagnostic purposes, in part because it cannot be grown on artificial media. However, a breakthrough in culturing T. pallidum was reported in 2018 when researchers managed to grow the bacterium in a rabbit epithelial cell line (Sf1Ep) using a medium called 'Sf1Ep medium'. It's not used for routine diagnostic purposes, but for research only. The diagnosis involves direct microscopic examination, serologic tests, molecular tests and histopathology.
2Baird-Parker Agar (BPA)his is a selective medium for the isolation of Staphylococcus species. It has lithium chloride and glycine to inhibit the growth of Gram-negative bacteria and most Gram-positive bacteria except Staphylococcus. Egg yolk emulsion is added to detect lecithinase production and tellurite reduction. S. aureus colonies on BPA are black due to reduction of tellurite, and they exhibit a clear zone due to lecithinase activity on egg yolk.
3Mannitol Salt Agar (MSA), or Chapman AgarThis is a selective and differential medium. The high concentration of NaCl (~7.5%) selects for halophiles, organisms that can tolerate high salt concentrations, thereby favouring the growth of Staphylococcus species. Mannitol is the differential component: S. aureus ferments mannitol, lowering the pH of the medium, which results in a color change of the pH indicator from red to yellow. Thus, growth of S. aureus is indicated by yellow colonies.
4Blood Agar (BA)This is a nutrient-rich, differential medium that supports the growth of many organisms. S. aureus forms colonies that are round, smooth, and golden-yellow. This bacterium typically demonstrates β-hemolysis, which is complete lysis of red blood cells, resulting in a clear zone around the colonies. This hemolysis is due to the production of hemolysins by S. aureus.
5BACTECThis is not a traditional medium but a system for detecting the growth of M. tuberculosis by monitoring the release of C14O2 from C14 palmitic acid, which the bacteria metabolize. An increase in radioactive counts in the BACTEC instrument indicates the growth of bacteria.
6Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
7Middlebrook 7H9 BrothThis is a liquid medium that contains glycerol and Tween 80, which prevent clumping of mycobacteria. The growth of M. tuberculosis results in turbidity.
8Dubos’ MediumA liquid medium that contains a mixture of salts, fatty acids, and polysorbate. When M. tuberculosis grows in this medium, it causes the medium to become turbid.
9Pawlowsky MediumA potato-based medium. Growth of M. tuberculosis may be similar to that seen on the LJ Medium.
10Loeffler MediumA serum-based medium. M. tuberculosis colonies on Loeffler medium are small, dry, wrinkled, and off-white to yellow.
11Tarshis MediumA blood-based medium that can promote the growth of M. tuberculosis. The colonies appear similar to those on the LJ Medium.
12Dorset MediumAn egg-based medium. M. tuberculosis colonies appear similar to those on Petragnini Medium: small, round, buff-colored, and taking 3-4 weeks to develop.
13Middlebrook 7H11 AgarThis is a nutrient-rich medium similar to 7H10 but includes additional pyruvate for energy source, promoting more luxurious growth. The colonies of M. tuberculosis appear small, slightly domed, and rough with a butyrous consistency.
14Middlebrook 7H10 AgarA selective medium that contains oleic acid, albumin, dextrose, and catalase. The colonies of M. tuberculosis appear small, rough, and buff to white-colored, taking less time to appear compared to egg-based media.
15Lowenstein-Jensen (LJ) MediumAn egg-based medium that uses malachite green to suppress the growth of other bacteria and glycerol to stimulate the growth of Mycobacterium tuberculosis. The colonies of M. tuberculosis on LJ are non-pigmented, dry, rough, raised, irregular with a wrinkled surface, initially creamy-white, turning yellowish or buff-colored on further incubation.
16Liquid Media (such as Nutrient Broth)E. coli exhibits homogenous turbid growth within 12-18 hours. After prolonged incubation, pellicles may form on the surface of the media.
17Lysine Iron Agar (LIA)Used to determine the ability of an organism to decarboxylate or deaminate lysine and to form hydrogen sulfide. E. coli is typically lysine decarboxylase positive and H2S negative, so you would see a reaction of red/purple slant and purple/red butt with no black precipitate.
18Brilliant Green Agar (BGA)A selective medium that is used to isolate Salmonella species, but E. coli can grow on it, albeit not as well.
19Sorbitol-MacConkey agarA variant of MacConkey agar, used in detecting E. coli O157:H7, which does not ferment sorbitol, unlike most strains of E. coli.
20Urea Agar/BrothE. coli is typically urease negative, so no color change would be expected in this medium.
21Triple Sugar Iron (TSI) AgarE. coli typically produces an acid butt, acid slant, and gas, with no H2S production, indicating it ferments lactose, sucrose, and glucose.
22Tryptic Soy Agar (TSA)A general purpose medium. E. coli colonies are medium to large, with a shiny moist appearance.
23Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
24m-ENDO AgarE. coli colonies appear as green with a metallic sheen, indicating lactose fermentation.
25Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
26Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
27MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
28Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
29Nutrient Agar (NA)A non-selective medium. E. coli colonies are usually large, circular, grayish-white, moist, and smooth.
30Nickerson’s Medium or Bismuth Sulfite Glucose Glycine Yeast (BSGG)This medium is used to stimulate the production of germ tubes, a characteristic of Candida albicans.
31Cornmeal Agar with Tween 80It is used for the identification of Candida species by promoting the formation of chlamydospores, which is a characteristic of Candida albicans.
32CHROMagar CandidaThis differential medium allows for the isolation and identification of Candida species based on colony color. Candida albicans usually forms green colonies on this medium.
33Potato Dextrose Agar (PDA)Potato Dextrose Agar (PDA) consists of a nutrient-rich substrate, made from dehydrated Potato Infusion and Dextrose, ideal for robust mycological propagation. Agar provides the solidifying medium. Acidification, typically using sterile tartaric acid, adjusts the pH to 3.5 +/- 0.1 to create a more selective environment by inhibiting bacterial proliferation. Additionally, Chloramphenicol is incorporated as an antimicrobial agent to further suppress bacterial contamination, thereby facilitating the selective isolation of fungi.
34Nutrient AgarIt is a general-purpose medium. However, E. faecalis grows poorly on nutrient agar, which means it does not proliferate as well on this medium compared to the others listed, indicating a negative or poor growth.
35Blood AgarA differential medium used to identify bacteria based on their hemolytic properties. E. faecalis typically shows gamma-hemolysis on this medium, i.e., no hemolysis or change in the color of the medium.
36MacConkey AgarTraditionally used to isolate and differentiate Gram-negative bacilli, E. faecalis can grow on this medium, producing small, round, magenta pink colonies due to lactose fermentation, indicating a positive result.
37Azide Dextrose BrothA selective medium inhibiting Gram-negative bacteria, used for the isolation of streptococci and staphylococci from mixed samples. E. faecalis will show a positive growth resulting in a turbid appearance of the broth.
38Todd-Hewitt BrothA liquid enrichment medium used for the cultivation of fastidious organisms such as streptococci and enterococci. E. faecalis will lead to a turbid broth due to microbial growth.
39Enterococcosel AgarA selective and differential medium that inhibits the growth of Gram-negative bacteria and distinguishes enterococci based on their ability to grow in the presence of bile and hydrolyze esculin. E. faecalis will form small, black colonies on this medium due to esculin hydrolysis.
40Bile Esculin Agar (BEA)A selective and differential medium that differentiates group D Streptococci and Enterococci based on the ability to hydrolyze esculin in the presence of bile. E. faecalis hydrolyzes esculin, leading to the formation of a dark brown or black precipita
41Brain-Heart Infusion (BHI) Broth or AgarThis is a nutrient-rich medium that supports the growth of a variety of fastidious organisms, including E. faecalis. The typical phenotype of E. faecalis on BHI is small, round, and white colonies.
42Tryptic Soy Broth or Agar (TSB/TSA)A general-purpose medium that supports the growth of a broad spectrum of bacteria. E. faecalis on TSA will typically form small, round, and white colonies, indicating a positive growth.