• On the other hand, if it is a beta-galactoside, it is called beta-galactosidase, and is responsible for breaking down the disaccharide lactose into its monosaccharide components, glucose and galactose Both varieties of galactosidase are categorized under the EC number 3.2.1. (wikipedia.org)
  • Beta-galactosidase has many homologues based on similar sequences. (wikidoc.org)
  • A few are evolved beta-galactosidase (EBG), beta-glucosidase , 6-phospho-beta-galactosidase, beta-mannosidase, and lactase-phlorizin hydrolase. (wikidoc.org)
  • In recent years, beta-galactosidase has been researched as a potential treatment for lactose intolerance through gene replacement therapy where it could be placed into the human DNA so individuals can break down lactose on their own. (wikidoc.org)
  • Maternal, but not paternal, transmission of the targeted allele leads to beta-galactosidase activity in hippocampal and cerebellar neurons. (nih.gov)
  • Senescent cells show a distinctive feature called Senescent associated secretory phenotypes (SASP) which includes increased expression of p16 and Beta-galactosidase can be used as a marker for senescent cells. (ijpsr.com)
  • Beta-galactosidase -- The enzyme that splits lactose into glucose and galactose. (nih.gov)
  • If the galactoside is classified as an alpha-galactoside, the enzyme is called alpha-galactosidase, and is responsible for catalyzing the hydrolysis of substrates that contain α-galactosidic residues, such as glycosphingolipids or glycoproteins. (wikipedia.org)
  • β-galactosidase , also called lactase , beta-gal or β-gal , is a glycoside hydrolase enzyme that catalyzes the hydrolysis of β-galactosides into monosaccharides through the breaking of a glycosidic bond . (wikidoc.org)
  • However, the sugar cap of the nanoparticle is broken down by β-galactosidase , an enzyme that is overproduced in senescent cells. (gowinglife.com)
  • The enzyme, encoded by a 12-kb gene mapping on the long arm (Xq22.1 region) of the X chromosome, is constituted by a glycosylated subunit of approximately 55 kD, synthesized as an inactive precursor that undergoes maturation in endoplasmic reticulum (ER) and Golgi apparatus before being delivered to the lysosome to form a functional dimer. (bvsalud.org)
  • In Fabry disease, the gene called galactosidase alpha (GLA), that provides instructions for making an enzyme called alpha-galactosidase A (α-Gal A), does not function correctly. (staarclinicalstudy.com)
  • Promising Fabry Disease Pipeline Therapies in the various stages of development include PRX-102, migalastat, Lucerastat, Enzyme replacement therapy (ERT), 4D-310, Recombinant human alpha galactosidase A (agalsidase beta), and others. (usfinancialnewstoday.com)
  • Fabry Disease is a rare genetic disorder that prevents the body from making an enzyme called alpha-galactosidase A. This enzyme is responsible for breaking down a type of fat called globotriaosylceramide (Gb3 or GL-3) into building blocks that the body's cells can use. (usfinancialnewstoday.com)
  • Alpha-galactosidase is an enzyme that assists in the digestion of complex carbohydrates known as oligosaccharides. (wellvishealth.ca)
  • The hydrolysis of X-gal by B-galactosidase produces galactose, a blue colored compound. (wikipedia.org)
  • β-galactosidase is an exoglycosidase which hydrolyzes the β- glycosidic bond formed between a galactose and its organic moiety. (wikidoc.org)
  • β-galactosidase is important for organisms as it is a key provider in the production of energy and a source of carbons through the break down of lactose to galactose and glucose. (wikidoc.org)
  • These mice express a catalytically inactive fusion protein of the NH 2 -terminal part of HDAC2 and β-galactosidase, which fails to integrate into corepressor complexes with mSin3B. (aacrjournals.org)
  • We analyzed the power of Crz1p-ZZ to bind HA-Hrr25p by Traditional western blot evaluation and discovered that Crz1p-ZZ connected with both energetic and catalytically inactive HA-Hrr25p (Fig. 1C). (gasyblog.com)
  • Two recombinant forms of alpha-galactosidase are called agalsidase alfa (INN) and agalsidase beta (INN). (wikipedia.org)
  • Galactosidases have a variety of uses, including the production of prebiotics, the biosynthesis of transgalactosylated products, and the removal of lactose. (wikipedia.org)
  • To trace the activity of B-galactosidase a colorless analog of lactose is used, X-gal. (wikipedia.org)
  • Substrates of different β-galactosidases include ganglioside GM1, lactosylceramides, lactose , and various glycoproteins . (wikidoc.org)
  • One example is GOS, which are synthesized from lactose by enzymatic trans-galactosylation using β-galactosidases, achieving a degree of polymerization between 3 and 10 (Van Leeuwen et al. (springer.com)
  • The inactive allele contains a lacZ reporter gene for analysis of brain-specific imprinting. (nih.gov)
  • B-galactosidase is made up of 4 identical polypeptide chains, i.e. it has 4 identical subunits. (wikipedia.org)
  • In this study we demonstrate that MsGC-β3 does form active homodimers and also show that it is capable of forming heterodimers with the NO-sensitive subunits, although these heterodimers are inactive. (biologists.com)
  • If both give rise to proteins, the subunits combine to form functional β -galactosidase. (istudy.pk)
  • B-galactosidase can be used to track the efficiency of bacterial transformation with a recombinant plasmid in a process called Blue/White Color Screening. (wikipedia.org)
  • Therefore, when the bacteria is transformed with the recombinant plasmid B-galactosidase is inactive and the colonies appear white, but when bacteria are transformed with the original plasmid, lacking the target gene, B-galactosidase is active and the colonies appear blue. (wikipedia.org)
  • Galactosidases are enzymes (glycoside hydrolases) that catalyze the hydrolysis of galactosides into monosaccharides. (wikipedia.org)
  • [10] The active site of β-galactosidase catalyzes the hydrolysis of its disaccharide substrate via "shallow" (nonproductive site) and "deep" (productive site) binding. (wikidoc.org)
  • The amino-terminal sequence of β-galactosidase, the α-peptide involved in α-complementation, participates in a subunit interface. (wikidoc.org)
  • These structural features provide a rationale for the phenomenon of α-complementation, where the deletion of the amino-terminal segment results in the formation of an inactive dimer. (wikidoc.org)
  • Alpha complementation refers to the ability of β -galactosidase to be expressed as two protein fragments, which assemble to form a functional protein. (istudy.pk)
  • When the target gene is present, the alpha-fragment gene would be inactive and the alpha fragment won't be produced. (wikipedia.org)
  • When the target gene is not found in the vector, the alpha fragment gene would be active, producing the alpha fragment and allowing for B-galactosidase to gain its activity. (wikipedia.org)
  • We previously demonstrated an approach (Antibody-antigen Interaction Dependent Apoptosis (AIDA)) whereby a single anti-β-galactosidase intracellular single chain Fv antibody fragment, fused to inactive procaspase-3, induced auto-activation of caspase-3 after binding to the tetrameric β-galactosidase protein. (whiterose.ac.uk)
  • The vector has a short portion of the β -galactosidase gene (the alpha fragment), and the bacterial chromosome has the rest of the gene. (istudy.pk)
  • B-galactosidase forms the basis of lac z operon in bacteria which can be used to control gene expression. (wikipedia.org)
  • If DNA is inserted into the plasmid-borne gene segment, the encoded subunit is not made and β -galactosidase is not produced. (istudy.pk)
  • Overexpression of an inactive mutant of Cav-1 lacking the tyrosine phosphorylation site (Y14F) or an siRNA-mediated Cav-1 knock down also resulted in marked attenuation of IL-1β-induced iNOS gene expression and NO release from these cells, thus further implicating Cav-1 in this signaling cascade. (diabetesjournals.org)
  • In cells without an insert in the plasmid, β -galactosidase is active and splits X-gal to form a blue dye. (istudy.pk)
  • β-galactosidase synthesis stops when glucose levels are sufficient. (wikidoc.org)
  • Jointly these findings claim that both PDE8A and PDE8B play important roles to keep low cAMP TCN 201 amounts thereby suppressing relaxing steroidogenesis by keeping CEH/HSL inactive and Superstar protein appearance low. (ece-inhibitor.com)
  • In vitro analysis revealed that a putative switch-protein kinase regulator, RsbW, is capable of interacting directly with σ 66 , as well as phosphorylating its own antagonist, RsbV1, rendering it inactive. (plos.org)
  • Senescent cells are mitotically inactive but are viable. (ijpsr.com)
  • Increased expression of p16 and β -galactosidase can be used as markers to identify senescent cells. (ijpsr.com)
  • When B-galactosidase is separated into 2 fragments, it has the unique property of regaining enzymatic activity upon the rejoining of the inactive fragments. (wikipedia.org)
  • Fabry Disease (FD) (OMIM 301500) is a metabolic X-linked inherited lysosomal storage disorder that results from the deficient activity of Alpha-Galactosidase A (Alpha-Gal), a lysosomal hydrolase that cleaves neutral glycosphingolipids with terminal N-linked galactosyl moieties, mainly globotriaosylceramides (Gb3). (bvsalud.org)
  • Substrate specificities == The founding member of [[glycoside hydrolase]] family 147, BACOVA_05493 from ''Bacteroides ovatus'' is a β1,4-galactosidase. (cazypedia.org)
  • When both fragments are present they would come together to restore the activity of B-galactosidase. (wikipedia.org)
  • When β -galactosidase is expressed, the bacteria can degrade X-gal, which turns the bacterial colony blue. (istudy.pk)
  • β-galactosidase can catalyze two different reactions in organisms. (wikidoc.org)
  • Lack of alpha-galactosidase activity in leukocytes has been linked to Fabry Disease. (wikipedia.org)
  • In cells which have inducible NF-ƙB activity, the factor is isolated in a crypic, inactive state from the cytoplasm. (osri.asia)
  • Addition of Ca2+ caused an increase in β-galactosidase activity indicative of Crz1p activation (Fig. 3A). (gasyblog.com)
  • In cells overexpressing experienced no effect on β-galactosidase levels (data not demonstrated) indicating that the kinase activity of Hrr25p is necessary for negative rules of Crz1p. (gasyblog.com)
  • Some rarer phenotypes give normal serum levels of an inactive α1-antitrypsin. (southtees.nhs.uk)
  • This was first discovered by Herzenberg and co- workers who observed that N-acetylcysteine (NAC) inhibited HIV LTR-directed expression of .β-galactosidase enhanced by tumor necrosis factor-α (TNF-α) and phorbol ester in in vitro HIV model systems (Roederer et al . (osri.asia)