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The processes of lipid peroxidation in the cells of Chlorobium limicola IMV K-8 under the influence of copper (II) sulphate

机译:硫酸铜(II)影响下小球藻IMV K-8细胞脂质过氧化过程

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The effect of stressors, including heavy metal ions such as Cu2+, promotes activation of free radical processes in the cells of microorganisms, which causes changes in their physiological and biochemical properties and the structure of bacterial membranes. The aim of this work was to assess the influence of copper (II) sulphate on intensity of lipid peroxidation (LPO) of Chlorobium limicola IMV K-8 by measuring the content of primary (conjugated dienes and lipid hydroperoxides) and secondary lipid peroxidation products (TBA-reactive products). Microorganisms were cultivated at a temperature of 28 °C in GSB cultivation medium with exposure to light of wavelength 700–800?nm and intensity 40 lux. A suspension of C. limicola ?МV К-8 cells in the phase of exponential growth was treated for one hour with metal salt solution in concentrations 0.05–0.50 mM for investigation of the influence of copper (II) sulphate on its physiological and biochemical properties. The control samples did not contain any copper (II) sulphate. Biomass was determined by turbidity of diluted cell suspension by application of photoelectric colorimeter KFK-3. A mixture of n-heptane and isopropyl alcohol was added into cell-free extract for conjugated dienes determination. The samples were incubated at room temperature and centrifuged. Water was added into the supernatant and the samples were stirred. Ethanol was added to the heptanes phase and adsorption was measured at 233 nm. The content of lipid hydroperoxides was determined by a method based on protein precipitation by trichloroacetic acid followed by addition of ammonium thiocyanate. The concentration of TBA-reactive products in the cell-free extracts was determined by color reaction with malondialdehyde and thiobarbituric acid exposed to high temperature and acidity of the medium, which causes formation of trimetinic adduct with maximal absorption at 532 nm. It was shown that when CuSO4 was added to the incubation medium the content of conjugated dienes and lipid hydroperoxides increased with the enhancement of salt concentration. However, its value decreased by the seventh and eighth days of cultivation. The content of TBA-reactive products under the influence of copper (II) sulphate varied depending on the duration of cultivation and concentration of the metal. Its highest quantity was observed on the eighth day of cultivation. Thus it was determined that under the influence of CuSO4 the content of conjugated dienes, lipid hydroperoxides and TBA-reactive products increases. This indicates the increased activity of lipid peroxidation processes and the free radical chain reaction damage mechanism to lipids under these conditions.
机译:应激源(包括Cu2 +等重金属离子)的作用促进了微生物细胞中自由基过程的激活,从而导致其生理生化特性和细菌膜结构发生变化。这项工作的目的是通过测量初级(共轭二烯和脂质氢过氧化物)和次级脂质过氧化产物的含量来评估硫酸铜(II)对小球藻IMV K-8脂质过氧化强度(LPO)的影响( TBA反应性产品)。将微生物在GSB培养基中于28°C的温度下培养,暴露于波长700-800?nm和强度40 lux的光下。用浓度为0.05–0.50 mM的金属盐溶液处理指数生长期的C. limicola?МVК-8细胞悬浮液一小时,以研究硫酸铜(II)对其生理生化特性的影响。对照样品不包含任何硫酸铜(II)。通过使用光电比色计KFK-3通过稀释的细胞悬液的浊度来确定生物量。将正庚烷和异丙醇的混合物添加到无细胞提取物中以进行共轭二烯的测定。样品在室温下孵育并离心。将水添加到上清液中并搅拌样品。将乙醇添加到庚烷相中,并在233 nm处测量吸收。脂质氢过氧化物的含量通过以下方法测定:基于三氯乙酸沉淀蛋白质,然后添加硫氰酸铵的方法。通过与丙二醛和硫代巴比妥酸暴露于介质的高温和酸性条件下的显色反应,测定无细胞提取物中TBA反应产物的浓度,这导致形成三聚体加合物,并在532 nm处具有最大吸收。结果表明,当将CuSO4加入培养液中时,共轭二烯和脂质氢过氧化物的含量随盐浓度的增加而增加。但是,其价值在栽培的第七天和第八天下降。硫酸铜(II)影响下的TBA反应产物的含量随培养时间和金属浓度的不同而变化。在培养的第八天观察到其最高量。因此确定在CuSO4的影响下,共轭二烯,脂质氢过氧化物和TBA反应产物的含量增加。这表明在这些条件下脂质过氧化过程的活性增加以及自由基链反应损害脂质的机理。

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