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Alpha Haemolysis Lab Report

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Introduction
There are many reasons for knowing the identity of different microbes when presented with them. The reasons include identifying the causative agent behind the disease in a patient, understanding how it can be treated, as well as knowing the microbe that should be used for making the right antibiotics. With this being said, their correct identification is not only significant in a microbiology lab but also in the medical, manufacturing, and pharmaceutical fields. The first test used in the identification of unknown bacteria numbers 3 and 4 was the Gram stain, which was used to differentiate between gram-positive and gram-negative bacteria based on their different cell wall elements. The Gram stain procedure distinguishes between …show more content…

Such bacteria require an enriched environment as compared to bacteria that grow more easily. It is also used to differentiate hemolytic bacteria, particularly Streptococcus species, also making it a differential media in distinguishing the destruction of red blood cells caused by cytolytic toxins secreted by select bacteria. If the bacteria were to have Beta hemolysis, there would be a large area of clearing around the bacteria colony on the BAP. When Alpha hemolysis occurs, there is a blue-green tint on the bottom of the plate, as if it were bruised. With gamma hemolysis, there is actually no hemolysis, therefore no change in the agar would occur. A Hektoen Enteric Agar was used next which is both a selective and differential medium intended to separate and distinguish members of the Salmonella and Shigella species from other Enterobacteria. Bile salts and bromthymol blue and acid fuchsin dyes hinder the growth of most Gram-positive organisms. Lactose, sucrose, and salicin are fermentable carbohydrates in the HE agar that encourage this variation in growth and color. Ferric ammonium citrate that is in the agar allows the observer to see hydrogen sulfide creation by reacting with hydrogen sulfide gas to make a

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