1974
DOI: 10.1016/0014-5793(74)81230-5
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Microbial assimilation of methanol induction and function of catalase in Candida boidinii

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1974
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Cited by 134 publications
(55 citation statements)
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“…The reaction was started by the addition of 10 l of lysate from 30 ϫ 10 6 cells, and absorbance at 240 nm was measured for 2 min. The rate of decrease, reflecting catalase activity, was converted to activity by the extinction coefficient 4.36 ϫ 10 4 cm 2 / mol (31).…”
Section: Methodsmentioning
confidence: 99%
“…The reaction was started by the addition of 10 l of lysate from 30 ϫ 10 6 cells, and absorbance at 240 nm was measured for 2 min. The rate of decrease, reflecting catalase activity, was converted to activity by the extinction coefficient 4.36 ϫ 10 4 cm 2 / mol (31).…”
Section: Methodsmentioning
confidence: 99%
“…Catalase activity was measured spectrophotometrically at 240 nm by H202 degradation (Roggenkamp et al 1974), MOX activity by oxidation of ABTS with HzO 2 and peroxidase at 420 nm (Eggeling and Sahm 1978), and malate dehydrogenase by oxidation of NADH with oxaloacetate as a substrate (Bergmeyer and Bernt 1983). Measurement of fi-lactamase activity was performed by monitoring degradation of the chromogenic cephalosporin Nitrocefin at 395 nm and cytochrome c oxidase by oxidation of reduced cytochrome c monitored at 550 nm (Tolbert 1974).…”
Section: Methodsmentioning
confidence: 99%
“…In these cases, cell-free extracts were prepared by X-pressing and centrifugation (Emri et al, 1997). Specific catalase (Roggenkamp et al, 1974) and glutathione peroxidase (GPx; Chiu et al, 1976) activities were measured. Briefly, catalase and GPx activities were determined spectrophotometrically, measuring H 2 O 2 decomposition and NADPH diminution rates, respectively (Roggenkamp et al, 1974;Chiu et al, 1976).…”
mentioning
confidence: 99%
“…Specific catalase (Roggenkamp et al, 1974) and glutathione peroxidase (GPx; Chiu et al, 1976) activities were measured. Briefly, catalase and GPx activities were determined spectrophotometrically, measuring H 2 O 2 decomposition and NADPH diminution rates, respectively (Roggenkamp et al, 1974;Chiu et al, 1976). In the GPx assay, cumene hydroperoxide was used as substrate and the glutathione disulphide formed was reduced by glutathione reductase auxiliary enzyme, which oxidizes NADPH cofactor (Chiu et al, 1976).…”
mentioning
confidence: 99%