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METHOD TO DETERMINE INTENSITY OF LIPID PEROXIDATION OF BASIDIOMYCETES CULTURES

机译:测定芽孢杆菌培养物脂质过氧化强度的方法

摘要

A method to determine the intensity of lipid peroxidation of basidiomycetes, which comprises obtaining a cultural filtrate, homogenizing the mycelium, adding to the mycelial homogenate and the cultural filtrate of solutions of trichloracetic acid and thiobarbituric acid and incubating the reaction mixture on a boiling water bath, cooling, centrifuging and spectrophotometric measurement of extinctions of test samples against control ones at a wavelength of =532 nm. Prior to the homogenization the mycelium is cooled, then the cooled mycelium is homogenized for three times at a temperature less than or equal to +5 °C, the 1time the mycelium, 2 after adding 2.0 ml of 22.5 % trichloracetic acid, 3 2.0 ml of 0.6 % solution of thiobarbituric acid, the mixture is incubated for 15 min, cooled up to +20 °C, centrifuged, extinction of test samples is measured against a control one (of 0.5 ml of distilled water) at wavelengths of 532 nm and 590 nm, the amount of the lipide peroxidation products reacting with thiobarbituric acid is calculated in nmol/g of absolutely dry mycelium biomass or per ml of the cultural filtrate.
机译:一种测定担子菌脂质过氧化强度的方法,该方法包括获得培养滤液,匀浆菌丝体,向菌丝匀浆和三氯乙酸和硫代巴比妥酸溶液的培养滤液中添加,然后在沸水浴上孵育反应混合物。 ,冷却,离心和分光光度法测定受测样品在= 532 nm波长下相对于对照的消光性。在均质化之前,先将菌丝体冷却,然后将冷却的菌丝体在小于或等于+5°C的温度下均质3次,一次是菌丝体,再添加2.0 ml的22.5%三氯乙酸,3个2.0 ml的匀浆。稀释0.6%的硫代巴比妥酸溶液,将混合物孵育15分钟,冷却至+ 20°C,离心,在532 nm波长下与对照样品(0.5 ml蒸馏水)对比,测定测试样品的消光在590 nm处,与硫代巴比妥酸反应的脂质过氧化产物的量以nmol / g绝对干燥的菌丝体生物量或每ml培养滤液计算。

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