1994
DOI: 10.1021/bk-1994-0566.ch010
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Cellulase Assays

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Cited by 76 publications
(77 citation statements)
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“…27 For the inhibition studies, the inhibitor stock of T1, T2, and T3 prehydrolyzates were mixed with the buffer such that their concentrations were 15, 20, 25, 30, and 35 g L –1 . The filter paper, buffer, and inhibitor mixture were equilibrated at 50 °C for 5 min in a reciprocating water bath agitated at 100 rpm.…”
Section: Methodsmentioning
confidence: 99%
“…27 For the inhibition studies, the inhibitor stock of T1, T2, and T3 prehydrolyzates were mixed with the buffer such that their concentrations were 15, 20, 25, 30, and 35 g L –1 . The filter paper, buffer, and inhibitor mixture were equilibrated at 50 °C for 5 min in a reciprocating water bath agitated at 100 rpm.…”
Section: Methodsmentioning
confidence: 99%
“…Before carrying out the enzymatic hydrolysis of raw Arundo donax L. and the CRR, the enzymatic activity of commercial preparation Cellic ® CTec2 was quantified through the standard NREL protocol [93]. 0.5 mL of a diluted sample containing enzymes was incubated with 50 mg of Whatman No.1 filter paper strip (Whatman, Maidstone, UK) and 1.0 mL of sodium citrate buffer at 50 • C for 1 h. The enzymatic reaction was terminated by adding 3.0 mL of 3,5-dinitrosalicylic (DNS) agent at 95 • C for 5 min.…”
Section: Enzymatic Hydrolysis Of Arundo Donax Lmentioning
confidence: 99%
“…Activities of both the glycosidases were expressed as micromoles of reducing sugars released from the polysaccharide substrates in 1 min (U). The filter paper activity was determined at pH 5.0 and 50°C according to Adney and Baker (2008) and expressed as FPU/mL. Total reducing sugars and glucose concentrations in NS-22086 were assayed as described below.…”
Section: Enzyme Preparationmentioning
confidence: 99%