1926
DOI: 10.1016/s0021-9258(18)84465-9
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Notes on Sugar Determination

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Cited by 1,607 publications
(212 citation statements)
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“…The enzyme-catalyzed reaction was measured with 2.5mg/ml soluble laminarin as a substrate in a 40mM potassium phosphate buffer, pH 7.0, at 30°C, for 15 min to obtain the reaction-time course. The reducing power caused by the enzymatic reaction from the substrate was determined by Somogyi-Nelson a method by which absorbance at 600 nm was measured (Somogyi, 1945). One unit of the enzyme was defined as the ˶ amount of enzyme ˵ , which liberates 1μmol of reducing sugar equivalent to glucose per one min under the standard assay conditions.…”
Section: 3β-13 Glucanase (Laminarinase)mentioning
confidence: 99%
“…The enzyme-catalyzed reaction was measured with 2.5mg/ml soluble laminarin as a substrate in a 40mM potassium phosphate buffer, pH 7.0, at 30°C, for 15 min to obtain the reaction-time course. The reducing power caused by the enzymatic reaction from the substrate was determined by Somogyi-Nelson a method by which absorbance at 600 nm was measured (Somogyi, 1945). One unit of the enzyme was defined as the ˶ amount of enzyme ˵ , which liberates 1μmol of reducing sugar equivalent to glucose per one min under the standard assay conditions.…”
Section: 3β-13 Glucanase (Laminarinase)mentioning
confidence: 99%
“…For quanti cation of reducing and total soluble sugars, powdered seeds incubated in 80 % ethanol (70 0 C for 90 min) were centrifuged at 14000 rpm for 10 min followed by supernatant extraction in rotary evaporator. The residuals obtained were dissolved in 0.5 mg/ml de-ionized water and the absorbance was noted at 620 nm and 490 nm, respectively (Nelson 1944;Somogyi 1952;Focks and Benning, 1998). For determination of galactomannan content, the dried residuals of powdered seeds extracted in phosphorus pentoxide (P 2 O 5 ) and ethanol were hydrolyzed in 2 M tri uoroacetic acid (TFA) followed by membrane lteration and de-ionization in C 18 column.…”
Section: Quanti Cation Of Proteins Sugars and Galactomannanmentioning
confidence: 99%
“…The 16S rRNA genes were selectively amplified (Somogyi, 1952). PCR reaction conditions were carried out according to Beffa et al (1996), and the PCR product was cloned into the pGEM-T vector system.…”
Section: Dna Isolation and 16s Rrna Gene Sequence Analysismentioning
confidence: 99%