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Molecular Genetics and the Study of Structure and Functions of Genes - Lab Report Example

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This lab report presents the study of the structure and functions of genes at the molecular level. Salmonella genus belongs to the family Enterobacteriaceae. The bacteria are gram-negative and facultatively anaerobic. The genus includes non-spore forming rods…
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Molecular Genetics and the Study of Structure and Functions of Genes
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2mL of molten overlay agar (kept in a 45°C water-bath) was added into a sterile tube. After waiting for the agar to cool slightly (roughly 37°C), 0.1mL of the bacterial culture was added using a Gilson pipette fitted with a sterile tip. Immediately the molten agar was poured along with the bacterial strain onto an E-medium plate ensuring even distribution of the overlay agar on the plate surface. The plate was then allowed to cool before incubating at 37°C overnight. 2mL of molten overlay agar was added into a sterile tube and after slightly cooling, 0.2mL 0.5mM histidine + 0.

5mM biotin solution was added. 0.1 mL of the bacterial culture was added using a Gilson pipette fitted with a sterile tip and immediately the molten agar was poured along with the bacterial strain onto an E-medium plate ensuring even distribution of the overlay agar on the plate surface. The plate was then left to cool and later incubated at 37°C overnight. 2mL of molten overlay agar was added into a sterile tube. After the agar had slightly cooled, 0.2mL 0.5mM histidine + 0.5mM biotin solution and 0.

1mL of the 0.1M histidine solution was added. Immediately pour the molten agar was poured onto an E-medium plate ensuring even distribution of the overlay agar on the plate surface and the plate allowed to cool. Six serial dilutions of the bacterial culture in ¼ strength Ringer’s solution ( 10-1, 10-2, 10-3, 10-4, 10-5 and 10-6) were prepared by adding, for instance for the 10-1, 100μl of the bacterial culture in a sterile Eppendorf tube and adding 900μl of ¼ strength Ringer’s solution.

The plate was divided into two halves using a marker pen and marking the bottom of the plate one side was marked 10-5 and the other side 10-6. 10μl of the 10-5 dilution was dropped using a Gilson pipette and spread using a glass spreader on one side of the plate and a further 10μl of the 10-6 dilution was dropped and spread using a glass spreader on the other side of the plate.

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