Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:3.2.1.31 (beta-glucuronidase)
 7,680 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

A sensitive and reliable assay for uridine 5'-diphosphoglucuronic acid (UDPGA) was developed that involved conjugation of diethylstilbestrol (DES) in vitro. This conjugation reaction is solely dependent upon UDPGA concentration. The assay uses 0.13 M Tris-HCl, pH 7.4, 6.7 mM MgCl2, 0.05% Brig 58, 0.25 mg guinea pig liver microsomal protein, 0.13 mM 3H-DES (0.2 microCi/ml), and 200 microliters of boiled 10% liver homogenate in a total volume of 0.5 ml. After a 60-min incubation at 37 degrees C, unconjugated DES is extracted into 5 ml of chloroform and the residual metabolized 3H-DES in the aqueous phase is determined by liquid scintillation spectrometry. After addition of beta-glucuronidase to the aqueous phase, about 90% of the radioactivity could be extracted into chloroform, demonstrating the DES-glucuronic acid is the primary metabolite. Thus, this method easily permits quantitation of UDPGA in rat liver in the 1-10 nmol range.
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PMID:Determination of hepatic uridine 5'-diphosphoglucuronic acid concentration by conjugation with diethylstilbestrol. 709 97

A 5-kDa polypeptide, pseudothionin Solanum tuberosum 1 (Pth-St1), which was active against Clavibacter michiganensis subspecies sepedonicus, a bacterial pathogen of potatoes, has been purified from the buffer-insoluble fraction of potato tubers by salt extraction and HPCL. Pth-St1 was also active against other potato pathogens tested (Pseudomonas solanacearum and Fusarium solani). The N-terminal amino acid sequence of this peptide was identical (except for a N/H substitution at position 2) to that deduced from a previously reported cDNA sequence (EMBL accession number X-13180), which had been misclassified as a Browman-Birk protease inhibitor. Pth-St1 did not inhibit either trypsin or insect alpha-amylase activities, and, in contrast with true thionins, did not affect cell-free protein synthesis or beta-glucuronidase activity. Northern-blot and tissue-print analyses showed that steady-state mRNA levels were highest in flowers (especially in petals), followed by tubers (especially in the epidermal cell layers and in leaf primordia), stems and leaves. Infection of leaves with a bacterial pathogen suspended in 10 mM MgCl2 switched off the gene, whereas mock inoculation with 10 mM MgCl2 alone induced higher mRNA levels.
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PMID:Pseudothionin-St1, a potato peptide active against potato pathogens. 803 86

Previous investigations failed to demonstrate mast cells in the alimentary tract and extraparietal glands of the ferret. It was decided therefore to test this and assess factors that may be of influence. Major salivary glands and tongues of mature ferrets, which had been fixed in formalin-calcium, were examined by means of light microscopical histochemistry. Staining of paraffin sections with techniques depending on basic dyes or esterolytic activity was carried out for conventional times with and without previous oxidation, hot acid hydrolysis, and trypsin and beta-glucuronidase digestion. Aldehyde fuchsin and high iron diamine consistently revealed the presence of few mast cells in interstitial stroma of salivary glands and lingual musculature, and in the lamina propria of lingual mucosa. Alcian blue at 0.5 M MgCl2 and safranin produced less consistent results, and even fewer metachromatic mast cells were detected. No staining of mast cells was obtained with the technique for naphthol AS-D chloroacetate esterase. Pretreatment did not increase the numbers and/or staining reactions of mast cells. The results refute the previous misconception and suggest that ferret is a species with a low incidence of mast cells largely expressing a connective-tissue phenotype.
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PMID:Mast cells in the salivary glands and tongue of the ferret: demonstration and some histochemical observations. 1726 66