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Lactose Uptake Driven by Galactose Efflux in Streptococcus
Lactose Uptake Driven by Galactose Efflux in Streptococcus

... proton symport and a lactose permease (18). That galactosefermenting mutants of S. thermophilus could be derived from wild-type Gal- strains (21), and that the former transported galactose at a significantly greater rate than the Galparental strains, would support the presence of distinct galactose ...
Cloning and nucleotide sequence of a gene upstream of the eaeA
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... alvei, and E. coli strain RDEC-1 that causes diarrhea in rabbits, and is thought to be a hot spot for insertion of virulence factor genes in the E. co/i chromosome. Lai and Donnenberg [ 161 reported that genes located between eueA and eaeB as well as downstream of eaeB are required for attaching and ...
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... protein phosphatase-1, the enzyme is in activated to phosphorylase b in a reaction that involves hydrolytic removal of the phosphate from the serine residue. Reactivation requires rephosphorylation with ATP and a specific enzyme, phosphorylase kinase ...
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... effects of ad libitum or restricted intake of moderate-energy diets during the entire dry period on pre-partum metabolism and post-partum metabolism and performance. A corn silage-based diet (26% of diet dry matter) providing 0.72 Mcal/lb during the far-off dry period (first 5 wk of an 8wk dry perio ...
Chapter 15 Cori and Alanine Cycles: Cori Cycle: Occurs between
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... Glucose from Fatty Acids: →Usually, fatty acids have an even number of carbon atoms FAeven →→ Acetyl-CoA X which is not converted to glucose FAodd →→ Acetyl-CoA + a single propionyl-CoA→ proprionate→oxaloacetate TAG → glycerol backbone → DHAP →glucose ...


... iii) Why are transport proteins (e.g. K+ channel) considered (at least by me) to be enzymes, even though they do not change the chemical structure of the substrate? (1 pt) i) Good substrates have many interactions with the active site, leading to small off-rates. Therefore the substrate is bound lon ...
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GENETICS TEST IV - Daytona State College
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... 6. The enzyme glucose oxidase isolated from the mold Penicillium notatum catalyzes the oxidation of β-D-glucose to D-glucono-δ-lactone. This enzyme is highly specific for the β anomer of glucose and does not affect the α anomer. In spite of this specificity, the reaction catalyzed by glucose oxidas ...
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... separating and growing them on selective media. A mbp1/swi4 double mutant was isolated using this technique in order to assess the activity of C. albicans MBP1. B) Gene disruptions of MBP1 via Geneticin (G418) resistance cassette (KNMX4) in YJJ1000 strain and Swi4 disruption using a URA3 cassette in ...
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... NAD is reduced to NADH2 by accepting electrons during glycolytic conversion of glucose to pyruvate NADH2 in turn reduces pyruvate with oxidation of NADH2 to NAD which supports continued anaerobic glycolysis, and generation from pyruvate of alcohols, carboxylic acids, and CO2 gas End products of gluc ...
intolerance to lactose and other dietary sugars
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... (Madzarovova-Nohejlova, 1973). Given the unusual distribution of the disaccharide, deficiency has not been of any nutritional consequence until recently, but it may become a problem because of its introduction as a sweetener in foods. Sodium-Dependent Glucose Transporter (SGLT1). SGLT1 is encoded by ...
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... Specimen: urethral,cervical smears &swabs (transport medium). Gram film: intracellular Gram -ve diplococci Culture: selective media Oxidase +ve acid production from glucose Latex agglutination ...
NEISSERIA
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... Specimen: urethral,cervical smears &swabs (transport medium). Gram film: intracellular Gram -ve diplococci Culture: selective media Oxidase +ve acid production from glucose Latex agglutination ...
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... this, the reactions may occur faster. Enzymes are organic catalysts. They are proteins. 2. The amino acids that make up these enzymes allow a tertiary and/or quaternary structure. Because each enzyme has a specific amino acid sequence, enzymes have a specific three-dimensional shape. 3. The molecule ...
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... reducing sugars and the beta linkages would be hydrolyzed by a beta-galactosidase. Similarly, connecting glucose as a glucopyranoside to galactose also gives 8 possible types of linkage. These are all reducing sugars and the alpha type of linkage would be cut by an alpha glucosidase. Finally, the tw ...
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... • Acts primarily on the liver, where it stimulates glycogenolysis and gluconeogenesis and thus increases hepatic glucose output. Glucagon also stimulates ketogenesis, providing an alternative fuel for those tissues that can use it and sparing glucose for those that cannot do without. • Also causes l ...
reprint - Oleg Igoshin
reprint - Oleg Igoshin

... Similarly, cotranscription of multiple (redundant) gene regulators from the same operon results in increased CV in the regulated gene as compared to the uncoupled regulator configuration (Figures 2D and S1E, N). Here, we assumed that the gene regulatory logic was an OR gate (i.e., each regulator by ...
Gluconeogenesis
Gluconeogenesis

... Introduction  Glucose remains the nearly universal and building ...
Glucose Metabolism
Glucose Metabolism

... A. Glucose in the bloodstream comes from the digestion and/or from glycogen stored in the liver and muscle. B. When glucose in the bloodstream enters the cytosol (internal fluid) of our cells, it is immediately converted to glucose – 6 – phosphate. 1. This is an exergonic process and not reversible. ...
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Lac operon



lac operon (lactose operon) is an operon required for the transport and metabolism of lactose in Escherichia coli and many other enteric bacteria. Although glucose is the preferred carbon source for most bacteria, the lac operon allows for the effective digestion of lactose when glucose is not available. Gene regulation of the lac operon was the first genetic regulatory mechanism to be understood clearly, so it has become a foremost example of prokaryotic gene regulation. It is often discussed in introductory molecular and cellular biology classes at universities for this reason.Bacterial operons are polycistronic transcripts that are able to produce multiple proteins from one mRNA transcript. In this case, when lactose is required as a sugar source for the bacterium, the three genes of the lac operon can be expressed and their subsequent proteins translated: lacZ, lacY, and lacA. The gene product of lacZ is β-galactosidase which cleaves lactose, a disaccharide, into glucose and galactose. LacY encodes lactose permease, a protein which becomes embedded in the cytoplasmic membrane to enable transport of lactose into the cell. Finally, lacA encodes galactoside O-acetyltransferase. Layout of the lac operon.It would be wasteful to produce the enzymes when there is no lactose available or if there is a more preferable energy source available, such as glucose. The lac operon uses a two-part control mechanism to ensure that the cell expends energy producing the enzymes encoded by the lac operon only when necessary. In the absence of lactose, the lac repressor halts production of the enzymes encoded by the lac operon. In the presence of glucose, the catabolite activator protein (CAP), required for production of the enzymes, remains inactive, and EIIAGlc shuts down lactose permease to prevent transport of lactose into the cell. This dual control mechanism causes the sequential utilization of glucose and lactose in two distinct growth phases, known as diauxie.
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