1998
DOI: 10.1016/s0963-9969(98)00077-5
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Purification and characterization of an acid phosphatase from cell membrane fraction of Lactococcus lactis ssp lactis 303

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Cited by 14 publications
(17 citation statements)
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“…Phagocytosis is considered an important way to control and eliminate invaders. It is well known that the life cycle, food supply, diseases, pollutants and other environmental stress affect the circulating haemocyte count both in quantity and quality [9,43]. In addition, the circulating haemocytes and non-circulating haemocytes exist in a state of dynamic flux [20].…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Phagocytosis is considered an important way to control and eliminate invaders. It is well known that the life cycle, food supply, diseases, pollutants and other environmental stress affect the circulating haemocyte count both in quantity and quality [9,43]. In addition, the circulating haemocytes and non-circulating haemocytes exist in a state of dynamic flux [20].…”
Section: Discussionmentioning
confidence: 99%
“…One unit of enzyme specific activity was defined as the amount of enzyme being able to release 1 mM p-nitrophenol per minute per mg serum protein under the assay conditions. Acid phosphatase (EC 3.1.3.2) activity in serum was determined with spectrophotometric method [43]. A tube containing 0.2 ml serum, 0.5 ml 0.1 M sodium citrate buffer (pH 4.8) and 0.2 ml 10 mM p-nitrophenol phosphate (Sigma) was incubated in a 37 C water bath for 30 min.…”
Section: Indices Examinationmentioning
confidence: 99%
“…Subcellular fractions Subcellular fractions were prepared according to Akuzawa & Fox (1998) and Coolbear et al (1992). From 100 mL of culture, 16.6 mL of loosely associated cell wall fraction (F1), 4.7 mL of cell wall lysate fraction (F2), 14 mL of cytoplasmic fraction (F3) and 2.7 mL of cell membrane fraction (F4) were obtained.…”
Section: Methodsmentioning
confidence: 99%
“…Enzyme activity was determined by a modification of the method used by Akuzawa and Fox (1998), with slight modifications as described by Miura et al (2010). Enzyme sample (100 mL) was added to 100 mL of 10 mM p-nitrophenylphosphate (p-NPP; Sigma Chemicals, St. Louis, MO, USA) in 10 mM sodium acetate (pH 5.2) and incubated for 30 min at 50 C. The reaction stopped by 200 mL of 1 M NaOH and absorbance was measured at 405 nm.…”
Section: Assay For Phosphatase Activitymentioning
confidence: 99%