Abstract
Desulfuromonas acetoxidans obtains energy for growth by the anaerobic oxidation of organic compounds with the carbon dioxide formation. It was found that ferrum and manganese are used as terminal electron acceptors in the processes of anaerobic respiration, such as dissimilative Fe3+- and Mn4+-reduction, carried out by these bacteria (Lovely, 1991). D. acetoxidans ІМV B-7384 can be used as anode biocatalyst in microbial fuel cell with high electron recovery through acetate oxidation to the electric current as a result of electron transfer to the anode or 3d-type transition metals, such as ferrum and manganese, in the process of their reduction. Investigation of biochemical changes of D. acetoxidans ІМV B-7384 under the influence of Fe (III) compounds is important for optimization of the process of bacterial electricity generation. ATP-hydrolase is located in cytoplasmic membrane, and its subunits are exposed to both the cytoplasm and the external environment. Therefore, the changes of that enzyme activity can be used as an indicator of various stress exposure. Presence of ferric iron ions in the bacterial growth medium could catalyze generation of organic reactive oxygen species, such as peroxyl (ROO-) and alkoxyl (RO-) radicals. Lipid peroxidation is one of the main reasons of cell damage and it’s following death under the influence of reactive oxygen metabolites. It is known that lipid peroxidation and membrane transport processes are somehow interrelated, but mechanisms of such interaction are still unidentified. In our previous researche we have shown the influence of ferric (III) citrate on the intensity of lipid peroxidation of D. аcetoxidans ІМV В-7384. Significant increase of the content of lipid peroxidation products (lipid hydroperoxides, conjugated dienes and malondialdehyde) in bacterial cells has been observed under the addition of ferric (III) citrate into the cultural medium. The increase of the concentration of lipid peroxidation products in bacterial cells confirms free radical mechanism of oxidation of polyunsaturated fatty acids. Thus, for fulfiling complete analyses of cell response against oxidative stress it was reasonable to investigate the influence of ferric (III) citrate on specific ATP-hydrolase activity, Na+, K+-ATP-hydrolase activity and Mg2+-ATP-hydrolase activity of D. acetoxidans ІМV В-7384. Bacteria were cultivated in the modified Postgaite C medium during four days under the anaerobic conditions and temperature +27°С with addition from 10 to 20 mM of ferric (III) citrate into the growth medium. Control samples didn’t contain investigated metal salt. Chosen concentrations of metal salt caused inhibition of bacterial growth by 20–50%. Activities of ATP-hydrolases were investigated as described. It was shown, that specific ATP-hydrolase activity of D. acetoxidans ІМV В-7384 is changing in dependance on duration of ferric (III) citrate exposure and concentration of the metal salt. Addition of the ferric (III) citrate in relatively low concentrations (10–12 mM) causes increasing of specific ATP-hydrolase activity of D. acetoxidans IMV B-7384 in comparison with control. Activity of investigated enzymes was inhibited under the increasing of metal salt concentration in bacterial growth medium. Increase of duration of D. acetoxidans IMV B-7384 cultivation causes decrease of ATP-hydrolase activity. Addition of ferric (III) citrate causes simultaneous increasing of Na+, K+-ATP-hydrolase activity and inhibition of Mg2+-ATP-hydrolase activity during four days of bacterial cultivation.
Highlights
Досліджено вплив різних концентрацій ферум (ІІІ) цитрату на АТФ-гідролази Desulfuromonas acetoxidans ІМВ В-7384 протягом чотирьох діб культивування
Investigation of biochemical changes of D. acetoxidans ІМV B-7384 under the influence of Fe (III) compounds is important for optimization of the process of bacterial electricity generation
In our previous researche we have shown the influence of ferric (III) citrate on the intensity of lipid peroxidation of D. аcetoxidans ІМV В-7384
Summary
Для досліджень використовували бактерії Desulfuromonas acetoxidans ІМВ В-7384, виділені з озера Яворівське, одержані в чистій культурі й ідентифіковані на кафедрі мікробіології Львівського національного університету імені Івана Франка. Для отримання мембранної фракції клітини руйнували ультразвуком і центрифугували за схемою, поданою нижче. Визначення загальної АТФ-гідролазної активності проводили у стандартному середовищі інкубації (об’єм – 0,4 мл) такого складу: 5 мМ АТФ, 5 мМ MgCl2, 50 мМ NaCl, 100 мМ KCl, 1 мМ етиленглікольтетраацетат (ЕГТА), 20 мМ трис-НCl, рН 7,4 та дигітонін 0,01%. Контролем (на неферментативний гідроліз АТФ та вміст ендогенного фосфору) були проби, що за своїм складом відповідали стандартному середовищу інкубації, але містили мембранний препарат, АТФ-гідролазну активність якого попередньо інактивували 10% розчином трихлороцтової кислоти. Визначення активності Na+, K+-АТФ-ази базується на здатності серцевого глікозиду уабаїну інгібувати цей фермент (Danilovich et al, 2004). Для цього визначали активність мембранного препарату в інкубаційному середовищі без додавання уабаїну та паралельно вимірювали АТФ-азну активність за присутності глікозиду (1 мМ). Na+, K+-АТФ-азну активність визначали як різницю величини активності у середовищі з уабаїном і без нього. Статистичне опрацювання результатів проводили з використанням критерію Стьюдента (Lakin, 1990)
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