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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.