Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:3.5.1.5 (urease)
 7,257 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Dielectric heating at frequencies of 42 and 2450 MHz was applied to whole soybeans of natural moisture content for varies exposure times. The minimum energy absorbed (MEA) was calculated from moisture-loss and temperature-elevation data. Biochemical analyses were performed to determine protein dispersibility index (PDI), nitrogen solubility index (NSI), and trypsin-inhibitor, urease, lipoxygenase, and peroxidase activities. Because the heating rates were different at the two frequencies for the power levels used, plots of the biochemical properties against temperature of exposure time showed an apparent frequency dependence. This dependence on frequency disappeared, however, when MEA was substituted as the independent variable. Chemical analyses revealed that dielectric heating of soybeans at natural moisture levels should be as effective as conventional steam toasting in reducing trypsin-inhibitor activity. PDI and NSI, but not urease, were suitable indicators of trypsin-inhibitor inactivation by dielectric heating. Lipoxygenase was completely inactivated by the dielectric-heating treatments that gave suitable trypsin-inhibitor inactivation, but peroxidase activity remained relatively high, offering possible advantages for bleaching and improved soy product color.
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PMID:Effects of 42- and 2450-MHz dielectric heating on nutrition-related properties of soybeans. 692 Apr 15

A microaerophilic nitrogen-fixing bacterium was isolated from surface-sterilized roots of Spartina alterniflora Loisel growing in a Nova Scotian salt marsh. It is a small curved rod and is motile with a single polar flagellum. Metabolism is respiratory. Organic and amino acids, but not carbohydrates, serve as carbon and energy sources. The guanine + cytosine content of its deoxyribonucleic acid is 32.1 +/- 1.0 mol%. Based upon morphological and biochemical characteristics this organism is assigned to the genus Camphlobacter Sebald and Veron 1963. It is distinguishable from other campylobacters by the presence of nitrogenase and urease, by the production of pigment from tryptophan, and by a combination of other biochemical traits. The association of this organism with plant roots further distinguishes it from other campylobacters which commonly inhabit animal, including human, tissues.
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PMID:Isolation of a nitrogen-fixing Campylobacter species from the roots of Spartina alterniflora Loisel. 693 66

We followed the "abbreviated precision protocol" of the National Committee for Clinical Laboratory Standards for the evaluation of precision, accuracy, and carryover in analysis for urea nitrogen with the multilayer film analysis system ("Ektachem"). We analyzed 456 clinical samples with this instrument, by the manual urease/glucose dehydrogenase method, and with the Beckman System I GLU/BUN Analyzer. Precision and accuracy were estimated for 50, 220, 270, and 500 mg/L urea nitrogen concentrations in 100, 30, or 20 microL of serum. Potential interference of 15 compounds was evaluated. Random error (defined as 1.965 X SD) was 7, 10, 12, and 18 mg/L. Systematic error was 3, 4, 5, and 15 mg/L. Total analytical error was 11, 14, 17, and 34 mg/L for analysis of 100 microL of serum at the above-stated urea nitrogen concentrations. The greatest interference (6 mg/L) was caused by ethanol (300 mg/L) and by hemoglobin (500 mg/L) in the urea nitrogen (at 260 mg/L) determination. Urea nitrogen concentration, as determined with the Ektachem was linearly related to the expected concentration, at least up to 1187 mg/L. Carryover was not statistically significant.
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PMID:Extended clinical trial and evaluation of urea nitrogen determination with the Ektachem GLU/BUN analyzer. 700 69

A mycobacterial strain known as Mycobacterial strain W was analysed for its growth characteristics and biochemical traits. This strain was found to be a rapid grower, with luxurient growth on Lowenstein-Jensen medium, Dubos agar, Middlebrook's agar and Sauton's medium. Colonies were smooth, convex and nonpigmented. Some of the colonies which appeared rough were similar to smooth colonies at least in biochemical characteristics. This organism was tolerant to wide range of temperatures and to chemical substances like thiophene - carboxylic acid hydrazide, isoniazid, sodium chloride but not to bile salts. It was negative for niacin production, for various amidases, urease production, 3 day arylsulfatase test and also for Tween 80 hydrolysis. On the other hand this strain was found to be positive for semiquantitative catalase, heat resistant catalase, nitrate reduction, sodium salicylate degradation, tellurite reduction, 14 day arylsulfatase test and fermentation of fructose. This organism could utilize sodium nitrate and sodium nitrite as sources of nitrogen but didn't exhibit any utilization of fructose, arabinose as only sources of carbon. Significance of these findings is discussed.
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PMID:A report on the biochemical analysis of Mycobacterium W. 702 33

Measurement of urinary urea excretion has been suggested as a means of estimating nitrogen balance in hospitalized patients who are malnourished. Because proficiency-testing surveys show gross variations in mean urea as determined by various automated methods and extremely poor precision occasionally, we compared urinary urea measurements and ammonia interference in three widely used methods. The coupled urease/glutamate dehydrogenase method (used in the DuPont aca) showed positive interference from ammonia, as expected; with the diacetylmonoxime (Technicon (12/60) and the urease conductivity (Beckman ASTRA) methods we saw no such interference. Generally, interference by ammonia is less than 10%, but (rarely) it may exceed 25%. However, if urine specimens are properly diluted and potential sources of interference recognized, all three methods appear capable of providing clinically useful data.
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PMID:Urinary urea: are currently available methods adequate for revival of an almost abandoned test? 708 63

The urease activity of 414 strains representing 21 species of the genus Bifidobacterium was surveyed. The strongest ureolytic strains belong mostly to the species B. suis and only a few to B. breve, B. magnum and "subtile" homology group. The study of some strongly ureolytic strains showed that urea and organic nitrogen concentration did not influence urease production. The high urease activity found also in the absence of urea suggested that this enzyme is not inducible. An ammonia concentration of 14 mM did not repress urease activity.
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PMID:Urease activity in the genus Bifidobacterium. 710 9

The effect of growth conditions on urease synthesis was studied with Staphylococcus saprophyticus L-1 isolated from natural sources. Urease biosynthesis was recorded in the absence of urea in the complete medium and in the conditions of nitrogen deficiency; the highest level of the enzyme biosynthesis was found when the culture was grown in the absence of amine nitrogen in the medium. Ammonium ions were a reversible inhibitor of urease and, at a high concentration (30 g of (NH4)2SO4 per litre of the medium), partly repressed its biosynthesis. The rate of growth was low when the cells were cultivated in flasks in a medium containing urea (20 g per litre of the medium). The growth was not inhibited when the cells were cultivated in 20-litre fermenters at the same concentration of urea, but with automatic pH regulation. The alkaline medium rather than urea contained in it appeared to be the principal factor inhibiting growth of the culture.
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PMID:[Urease synthesis regulation in Staphylococcus saprophyticus by urea and ammonia]. 715 6

The purpose of this paper is to investigate the specific metabolism of the protein and amino acid during pregnancy from a standpoint of urea nitrogen recycling hydrolyzed by intestinal bacterial urease of pregnant rat. For this purpose, the activity of urease of the intestinal flora, and L-glutamate dehydrogenase (GDH) in liver mitochondria, the concentration of free ammonia and urea in the intestinal tract, portal vein and right ventricle of the rat were discussed. The results were: 1) The activity of urease moderately increased during pregnancy with the peak on 19th gestational day. 2) The concentration of free ammonia in the intestinal tract elevated slightly, and markedly elevated in portal vein, but seemed to be no specific change in right ventricle. The peak showed on 19th gestational day. 3) The activity of GDH increased markedly during pregnancy, and the protein synthesis was thought to be accelerated. 4) Urea concentration in intestinal tract and blood stream seemed somewhat increased. This results revealed that the urea recycling system and protein synthesis accelerated during pregnancy because of high urease and GDH activity. This phenomenon adapted the pregnant to nutrient of the fetus for growing and development, and introduced a new concept of maternal-fetal unit of nutrition, especially in protein metabolism.
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PMID:[Studies on entero hepatic circulation of urea nitrogen in pregnant rat (author's transl)]. 724 Aug 47

A minor modification in the automated analytical system of the official AOAC semiautomated method for determining crude proteins results in an automated method for determining urea and ammoniacal nitrogen in animal feeds and their ingredients. Urease enzyme which has high activity, yields a clear solution in water, has low ammonia impurity, and is inexpensive is used in the automated method. Weights from 1 to 2.5 g feed sample are dissolved in water, and sample solutions are analyzed at the rate of 40 samples/h. Five AAFCO feed check samples were analyzed repeatedly by the automated method, and results were compared with the grand averages from the check sample reports. The official AOAC manual urease method was used by AAFCO participants. Average recovery of urea and ammoniacal nitrogen was 100.6% by the automated method relative to the AAFCO reported averages. The range of recoveries as 98.5-102.7%. The non-protein nitrogen (NPN) concentrations, expressed as protein equivalent, ranged from 3.40 to 63.04% protein on these samples. The average relative standard deviation for the automated analyses was 0.77%, compared with 1.54% for the manual method. This method is an important adjunct to laboratories using or considering use of the semiautomated method for crude protein and needing further information on NPN.
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PMID:Automated determination of urea and ammoniacal nitrogen (NPN) in animal feeds. 728 6

Hyphomicrobium species are able to use allantoin as a nitrogen source for growth. Allantoin is broken down to glyoxylate and ammonia by the consecutive action of allantoinase, allantoicase, ureidoglycolase and urease.
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PMID:Metabolism of allantoin in Hyphomicrobium species. 733 36


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