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Centennial Honors College Western Illinois University Undergraduate Research Day 2014 Poster Presentation Detection of Carbon Catabolite Repression in Leuconostoc Kara Chicoine, Eliese Potocek and Darrah Dunlap Faculty Mentor: Scott Holt Biology Leuconostoc is a gram-positive, lactic acid-producing bacterial genus that plays a large role in food and industrial fermentation. A defining feature of Leuconostoc is its’ ability to produce α-glucans (dextran), which are complex exopolysaccharides composed of glucose units. Leuconostoc makes the enzyme glucansucrase which catalyzes the production of α-glucans via catabolizing the sugar sucrose. The goal of this study was to determine if glucansucrase production by Leuconostoc is controlled by carbon catabolite repression (CCR). CCR is a global regulatory mechanism used by most bacteria to ensure that bacteria will preferentially consume simple sugars first (glucose) followed by more complex sugars (sucrose) when both are present in a culture medium. In this study, Leuconostoc strains (L. mesenteroides B-512F, B-1118, and L. citreum B1355, B-742) were cultivated for 3-h or 6-h at 30°C in media containing either glucose (G), sucrose (S), a mixture of glucose and sucrose (G/S), or a mixture of glucose and sucralose (G/Su). Glucansucrase activity patterns were determined for each sample (0h & 3-h or 6-h) using SDS-PAGE and in-situ detection of enzyme activity in the gels. Glucansucrase production for L. mesenteroides B-1118 was not significantly altered by any carbohydrate tested. The L. citreum strains and L. mesenteroides B-512F showed that glucansucrase production was not inhibited when the strains were grown in the (G/S) media, indicating that these strains are not controlled by CCR. Lack of a catabolite repression mechanism for Leuconostoc may indicate that metabolism of sucrose for energy and carbon is not the primary function of glucansucrase.