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Here's a paragraph about the molds that may help to infer the reason of the advantages during observation of mold colonies: 'Because the structural components of molds are very delicate, even simple handling with an inoculating loop may result in mechanical disruption of their components.The followi ng culture technique es used to to avoid this disruption. After culturing, molds spores are deposited in the surface of the agar and incubated in a moist chamber at room temperature. Direct microscopic observation is then possible without fear of disruption or damage to the anatomical components'. It may be more beneficial in this aspect: allowing a full and healthy growth of the mold, that is, with its complete structure, then to be able to proceed to look through the microscope maybe it form, type of spore,sporangia or mycelium. In short, ensure that the mold to grow properly. Maybe it's not what you exactly were looking for but it could help you!

Second Year of Microbiology bachelor's degree (University Of Puerto Rico in Arecibo) Paragraph taken of Capuccino/Sherman Microbiology. A laboratory Manual.Eight Edition. The following are some advantages of an agar plate verses a slant tube: 1. Surface area- An agar plate has a much larger surface area: a. Easier to isolate individual colonies using the streak-plate method.

Evaluate the colony shape, margin and elevation. Can grow a larger number of ce lls. Growth- An agar plate allows you to quantify the number of colonies on an agar plate, provided it is within the 30-300 range. Whereas the slant tube cannot quantify growth but only describes growth as none, slight, moderate, or large.

Study 5 Serial Dilution method flashcards from Mandy S. On StudyBlue. Advantages of serial dilution-agar plate; 1. Only viable cells counted. Plate 1 mL = 10^4. Many students have difficulties with dilution theory, particularly with serial dilutions. One ml of a turbid culture evenly over the surface of a nutrient agar plate, you would evenly. The buffer is called 'TE (pH 8.0)', and consists of 10 mM Tris-HCl, a pH. What are the advantages / disadvantages of each method?