1Lowenstein-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.
2Simmons 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.
3Cornmeal 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.
4Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
5Enterococcosel 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.
6CHROMagar 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.
7Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
8Mannitol 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.
9Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
10Todd-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.
11Blood 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.
12Blood 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.
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.
14Triple 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.
15Bile 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
16Urea Agar/BrothE. coli is typically urease negative, so no color change would be expected in this medium.
17Nickerson’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.
1Tryptic Soy Agar (TSA)A general purpose medium. E. coli colonies are medium to large, with a shiny moist appearance.
2Potato 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.
3Sabouraud 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.
4Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
5Sf1Ep 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.
6RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
7Middlebrook 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.
8Middlebrook 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.
9Pawlowsky MediumA potato-based medium. Growth of M. tuberculosis may be similar to that seen on the LJ Medium.
10Phenol 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.
11Simmons 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.
12Violet Red Bile Agar (VRBA)E. coli colonies are red (pink to red) and may show bluish fluorescence under UV light.
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.
14Nickerson’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.
15CHROMagar 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.
16Cornmeal 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.
17Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
18Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
19Enterococcosel 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.
20Brilliant Green Agar (BGA)A selective medium that is used to isolate Salmonella species, but E. coli can grow on it, albeit not as well.
21Blood 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.
22Todd-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.
23Triple 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.
24Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
25Bile 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
26Urea Agar/BrothE. coli is typically urease negative, so no color change would be expected in this medium.
27Blood 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.
1m-ENDO AgarE. coli colonies appear as green with a metallic sheen, indicating lactose fermentation.
2DNase 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.
3Potato 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.
4Sabouraud 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.
5Tryptic 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.
6Mannitol 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.
7Azide 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.
8Loeffler MediumA serum-based medium. M. tuberculosis colonies on Loeffler medium are small, dry, wrinkled, and off-white to yellow.
9Simmons 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.
10Petragnini 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.
11Violet Red Bile Agar (VRBA)E. coli colonies are red (pink to red) and may show bluish fluorescence under UV light.
12Cornmeal 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.
13Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
14Urea Agar/BrothE. coli is typically urease negative, so no color change would be expected in this medium.
15Nickerson’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.
16CHROMagar 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.
17Tarshis MediumA blood-based medium that can promote the growth of M. tuberculosis. The colonies appear similar to those on the LJ Medium.
18Dubos’ 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.
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.
20Nutrient 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.
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.
22Nutrient Agar (NA)A non-selective medium. E. coli colonies are usually large, circular, grayish-white, moist, and smooth.
23Sf1Ep 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.
24Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
25Brain-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.
26Dorset 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.
27Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
28Enterococcosel 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.
29Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
30Blood 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.
31Sauton’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.
32MacConkey 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.
33Lysine 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.
34Lowenstein-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.
35MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
36Middlebrook 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.
37Pawlowsky MediumA potato-based medium. Growth of M. tuberculosis may be similar to that seen on the LJ Medium.
38RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
39Middlebrook 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.
40Brilliant Green Agar (BGA)A selective medium that is used to isolate Salmonella species, but E. coli can grow on it, albeit not as well.
41Todd-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.
42Triple 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.
43Blood 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.
44Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
45Bile 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
1Sauton’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.
2Lysine 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.
3MacConkey 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.
4Lowenstein-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.
5Nutrient Agar (NA)A non-selective medium. E. coli colonies are usually large, circular, grayish-white, moist, and smooth.
6Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
7Dorset 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.
8MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
9Sf1Ep 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.
10Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
11Middlebrook 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.
12RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
13Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
14Enterococcosel 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.
15Todd-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.
16Blood 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.
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.
18Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
19Triple 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.
20Bile 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
21Urea Agar/BrothE. coli is typically urease negative, so no color change would be expected in this medium.
22Nickerson’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.
23CHROMagar 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.
24Tarshis MediumA blood-based medium that can promote the growth of M. tuberculosis. The colonies appear similar to those on the LJ Medium.
25Sabouraud 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.
26Potato 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.
27Sorbitol-MacConkey agarA variant of MacConkey agar, used in detecting E. coli O157:H7, which does not ferment sorbitol, unlike most strains of E. coli.
28Nutrient 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.
29Liquid 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.
30Tryptic 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.
31Mannitol 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.
32Azide 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.
33Brain-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.
34Loeffler MediumA serum-based medium. M. tuberculosis colonies on Loeffler medium are small, dry, wrinkled, and off-white to yellow.
35Pawlowsky MediumA potato-based medium. Growth of M. tuberculosis may be similar to that seen on the LJ Medium.
36Simmons 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.
37Violet Red Bile Agar (VRBA)E. coli colonies are red (pink to red) and may show bluish fluorescence under UV light.
38Petragnini 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.
39Cornmeal 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.
40Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
41Blood 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.
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.
2Potato 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.
3Lowenstein-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.
4Tryptic 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.
5Middlebrook 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.
6RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
7Pawlowsky MediumA potato-based medium. Growth of M. tuberculosis may be similar to that seen on the LJ Medium.
8Phenol 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.
9Simmons 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.
10Triple 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.
11Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
12Bile 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
13Urea Agar/BrothE. coli is typically urease negative, so no color change would be expected in this medium.
14Nickerson’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.
15Sabouraud 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.
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.
17Loeffler MediumA serum-based medium. M. tuberculosis colonies on Loeffler medium are small, dry, wrinkled, and off-white to yellow.
18Cornmeal 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.
19CHROMagar 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.
20Blood 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.
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.
22Nutrient 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.
23Sauton’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.
24MacConkey 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.
25Lysine 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.
26Nutrient Agar (NA)A non-selective medium. E. coli colonies are usually large, circular, grayish-white, moist, and smooth.
27Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
28Sf1Ep 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.
29Dorset 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.
30Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
31MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
32Middlebrook 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.
33Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
34Enterococcosel 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.
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.
36Blood 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.
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.
2Sabouraud 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.
3Potato 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.
4Tryptic 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.
5Mannitol 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.
6Phenol 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.
7Simmons 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.
8Violet Red Bile Agar (VRBA)E. coli colonies are red (pink to red) and may show bluish fluorescence under UV light.
9Petragnini 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.
10Cornmeal 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.
11Bile 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
12Urea Agar/BrothE. coli is typically urease negative, so no color change would be expected in this medium.
13Nickerson’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.
14Tarshis MediumA blood-based medium that can promote the growth of M. tuberculosis. The colonies appear similar to those on the LJ Medium.
15Dubos’ 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.
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.
17Loeffler MediumA serum-based medium. M. tuberculosis colonies on Loeffler medium are small, dry, wrinkled, and off-white to yellow.
18Brain-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.
19Nutrient Agar (NA)A non-selective medium. E. coli colonies are usually large, circular, grayish-white, moist, and smooth.
20CHROMagar 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.
21Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
22Liquid 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.
23Sorbitol-MacConkey agarA variant of MacConkey agar, used in detecting E. coli O157:H7, which does not ferment sorbitol, unlike most strains of E. coli.
24Nutrient 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.
25Sauton’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.
26MacConkey 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.
27Lysine 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.
28Lowenstein-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.
29Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
30Sf1Ep 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.
31Dorset 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.
32Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
33MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
34Middlebrook 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.
35RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
36Pawlowsky MediumA potato-based medium. Growth of M. tuberculosis may be similar to that seen on the LJ Medium.
37Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
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.
39Brilliant Green Agar (BGA)A selective medium that is used to isolate Salmonella species, but E. coli can grow on it, albeit not as well.
40Todd-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.
41Blood 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.
42Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
1Tarshis MediumA blood-based medium that can promote the growth of M. tuberculosis. The colonies appear similar to those on the LJ Medium.
2Proskauer and Beck’s MediumA liquid medium. The growth of M. tuberculosis causes turbidity.
3Dubos’ 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.
4Tryptic Soy Agar (TSA)A general purpose medium. E. coli colonies are medium to large, with a shiny moist appearance.
5Middlebrook 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.
6DNase 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.
7Potato 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.
8MacConkey 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.
9Lysine 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.
10Lowenstein-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.
11Dorset 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.
12Mueller Hinton Agar (MHA)Typically used for antibiotic susceptibility testing. E. coli colonies appear pale straw colored.
13MacConkey Agar (MAC)This selective and differential medium distinguishes lactose fermenters from non-fermenters. E. coli colonies are circular, moist, smooth, and pink.
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.
16Pawlowsky MediumA potato-based medium. Growth of M. tuberculosis may be similar to that seen on the LJ Medium.
17RPMI 1640 MediumIt is a rich medium that contains inorganic salts, glucose, amino acids, vitamins, and other nutrients that promote the growth of yeast cells.
18Phenol 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.
19Violet Red Bile Agar (VRBA)E. coli colonies are red (pink to red) and may show bluish fluorescence under UV light.
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.
21Baird-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.
22BACTECThis 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.
23Sabouraud 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.
24Liquid 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.
25Petragnini 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.
26Cornmeal 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.
27Eosin Methylene Blue (EMB) AgarA selective and differential medium where E. coli forms distinctive metallic green sheen colonies due to vigorous lactose fermentation.
28Enterococcosel 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.
29Brilliant Green Agar (BGA)A selective medium that is used to isolate Salmonella species, but E. coli can grow on it, albeit not as well.
30Todd-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.
31Blood 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.
32Triple 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.
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.
34Sorbitol-MacConkey agarA variant of MacConkey agar, used in detecting E. coli O157:H7, which does not ferment sorbitol, unlike most strains of E. coli.
35Tryptic 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.
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.
37Loeffler MediumA serum-based medium. M. tuberculosis colonies on Loeffler medium are small, dry, wrinkled, and off-white to yellow.
38Azide 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.
39Nutrient Agar (NA)A non-selective medium. E. coli colonies are usually large, circular, grayish-white, moist, and smooth.
40Blood Agar (BA)E. coli colonies on this differential medium are large, circular, gray, moist, and can show β-hemolysis.
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.
42Sula’s MediumA liquid medium containing glycerol, asparagine, and a variety of salts. The growth of M. tuberculosis results in turbidity.
43Urea Agar/BrothE. coli is typically urease negative, so no color change would be expected in this medium.
44Bile 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
45Nickerson’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.
46CHROMagar 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.
47Cystine Lactose Electrolyte-Deficient (CLED) AgarE. coli will give lactose-positive yellow colonies.
48Blood 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.