추천 제품
생물학적 소스
Escherichia coli K12
Quality Level
형태
solution
분자량
Mr ~220 kDa
포장
pkg of 1 mL (03707580001)
pkg of 15 mL (03707601001)
pkg of 5 mL (03707598001)
제조업체/상표
Roche
저장 조건
(Keep container tightly closed in a dry and well-ventilated place.)
파라미터
48 °C optimum reaction temp.
기술
activity assay: suitable
색상
colorless
최적 pH
6.0-6.5
solubility
water: soluble
적합성
suitable for enzyme test
UniProt 수납 번호
응용 분야
detection
sample preparation
저장 온도
2-8°C
유전자 정보
Escherichia coli ... uidA(946149)
일반 설명
Glucuronidase at 25 °C, or 140 U/mg at 37 °C, at pH 7 with 4-nitrophenyl-β-D-glucuronide as substrate; 1 ml β-Glucuronidase contains at least 140 U at 37 °C.
특이성
Cleaves terminal glucuronic acid which is β-linked to mono-, oligo- or polysaccharides or phenol.
애플리케이션
β-Glucuronidases have been used extensively in research and analytical laboratories for the enzymatic hydrolysis of steroid β-glucuronides. β-Glucuronidase is used:
- for the hydrolysis of steroid conjugates (glucuronides) in urine (pH 6.0–6.5)
- in doping analysis
- for the detection of benzodiazepine in small doses.
- during sample preparation to cleave off glucuronides prior to GC-MS, HPLC, immunoassays, or other analytical methods.
생화학적/생리학적 작용
Glucuronidation is one of the basic principles of metabolism. Many substances presented to the human body undergo metabolic processing that includes conjugation with glucuronic acid by UDP-glucuronosyltransferases (UGTs). β-Glucuronidase, also known as β-D-glucuronoside glucuronosohydrolase, catalyzes the transfer of a glucuronyl group to many biological and pharmacologically active endogenous and exogenous molecules. Glucuronide is in general, more soluble, less toxic, and more easily excreted by the human body compared to the original molecule. To analyze these drug conjugates that are present in body fluids, such as urine and plasma, deconjugation of the glucuronide is necessary. Enzymatic hydrolysis prior to detection is essential to achieving high sensitivity during analysis. After hydrolysis, the sample may be analyzed by mass spectroscopy, gas chromatography, HPLC, immunoassays, or other analytical methods.
특징 및 장점
β-Glucuronidase from E. coli is highly specific for β-glucuronides, and is capable of very quickly hydrolyzing steroid β-glucuronides as well as cleaving many other types of glucuronides, such as benzodiazepine, opioid, and cannabinoid. β-Glucuronidase is used for the enzymatic hydrolysis of glucuronides in biological fluids, primarily urine. Substances used for doping are conjugated with glucuronides, which means that effective doping analysis relies very often on the enzymatic cleavage of conjugated drug molecules by β-glucuronidase.
- Perform fast analysis due to the enzyme′s high specific activity.
- Quickly screen for steroids, benzodiazepines, cannabinoids, and opioids.
- Save time by developing your procedure without the need to clean up the reaction or buffer the urine.
단위 정의
The international unit of β-glucuronidase activity is the enzyme activity that increases the rate of release of 4-nitrophenol from 4-nitrophenyl-β-D-glucuronide (4NPG) at a temperature of +25 °C and pH 7.0 by 1 μM.
The Fishman unit was previously used. This unit is the release of phenolphthalein from its glucuronide (PPG). It is not possible to measure the relative activities of different preparations for steroid β-glucuronides by comparing their activities with respect to PPG. Many preparation do not catalyze the hydrolysis of PPG, 4NPG, or the various steroid β-glucuronides in urine equally. The choice of 4NPG as standard substrate is based on the following considerations:
The Fishman unit was previously used. This unit is the release of phenolphthalein from its glucuronide (PPG). It is not possible to measure the relative activities of different preparations for steroid β-glucuronides by comparing their activities with respect to PPG. Many preparation do not catalyze the hydrolysis of PPG, 4NPG, or the various steroid β-glucuronides in urine equally. The choice of 4NPG as standard substrate is based on the following considerations:
- The Michaelis concentrations for the two substrates are similar (KM = 2 ×10-4 M for 4 NPG and KM = 6 ×10-5 M for PPG), but the corresponding rates of hydrolysis differ:
- 4NPG is hydrolysed about 5 × as fast as PPG;
- For PPG, inhibition by excess substrate occurs; this is not observed using 4NPG.
물리적 형태
Solution in 50% glycerol, pH approximately 6.5
(15 ml in one bottle)
(15 ml in one bottle)
기타 정보
The E.coli β-glucuronidase enzyme is essentially free of sulfatase activity and is especially efficient in cleaving steroid and benzodiazepine conjugates.
For life science research only. Not for use in diagnostic procedures.
For life science research only. Not for use in diagnostic procedures.
법적 정보
The sale of the Product does not exhaust or grant any rights in third party patents including patents of companies of the F. Hoffmann - La Roche AG group of companies, in particular, for the use of modified antibodies obtained by using the product.
Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 1
Flash Point (°F)
No data available
Flash Point (°C)
No data available
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
Drug metabolism and disposition: the biological fate of chemicals, 27(9), 1064-1067 (1999-08-26)
Individuals exposed to carcinogenic aromatic amines excrete arylamine N- and O-glucuronide metabolites. This study assessed the susceptibility of selected glucuronides to hydrolysis by human and Escherichia coli beta-glucuronidase. N- or O-glucuronides were prepared with the following aglycones: benzidine, N-acetylbenzidine, N'-hydroxy-N-acetylbenzidine
LC-MS/MS-Based Assay for Free and Deconjugated Testosterone and Epitestosterone in Rat Urine and Serum.
Journal of Analytical and Bioanalytical Techniques, S5, doi-doi (2014)
The British journal of nutrition, 102(2), 195-200 (2009-07-10)
There has been a growing interest in lignans, a class of phyto-oestrogens, because of their potentially favourable effects on human health. The aim of the present study was to compare the metabolic profile of post-menopausal women consuming various amounts of
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