The aim of the present work was to investigate the influence of alkylhydroxybenzenes (AHBs) and tyrosol, which belong to cell differentiation factors d(1) group of autoregulators on properties of biodegradation enzymes, catechol 1,2-dioxygenase (Cat 1,2-DO) and methylcatechol 1,2-dioxygenase (MCat 1,2-DO) of Rhodococcus opacus 6a. AHBs were found to have a greater effect on MCat 1,2-DO than on Cat 1,2-DO. It was expressed by more pronounced changes in the activity of MCat 1,2-DO with unsubstituted catechol at different AHB concentrations and by increasing thermostability of MCat 1,2-DO compared to Cat 1,2-DO under the protective action of AHBs. The compound C(7)-AHB shifted the maximum of dioxygenase activities towards higher temperatures and increased their operation optimum. AHBs changed the specificity constant of dioxygenases by decreasing/increasing the K(m)/V(max) value. For example, the increase in the V(max) value of 3,6-dichlorocatechol oxidation by Cat 1,2-DO in the presence of C(7)-AHB was 300-fold higher compared to the same reaction without AHB. The influence of cell differentiation factors on the properties of dimeric enzymes has been shown for the first time. It gives an idea of how the specificity of enzymes can be changed in vivo when strains contact new substrates. The work has shown the possibility of modification of the properties of dimeric enzymes towards the extension of enzyme activity with difficulty converted substrates or in more extreme conditions, which may be important for biotechnological processes.
The strains Rhodococcus sp. 400, R. rhodochrous 172, and R. opacus 6a utilize 4-methylbenzoate as the only carbon and energy source. 4-Methylcatechol is a key intermediate of biodegradation. Its further conversion by all the strains proceeds via ortho-cleavage. The specific activity of catechol 1,2-dioxygenase assayed in crude extracts of Rhodococcus sp. 400 and R. rhodochrous 172 with 3- and 4-methylcatechols does not exceed the enzyme activity assayed with catechol. Two catechol 1,2-dioxygenases have been purified from the biomass of R. opacus strain 6a grown with 4-methylbenzoate. These enzymes differed in molecular mass and physicochemical and catalytic properties. One of these enzymes belongs to the type of enzymes cleaving the catechol ring and known as methylcatechol 1,2-dioxygenases. In bacteria of the Rhodococcus genus, such an enzyme is described here for the first time.
The role of phototrophs is examined in alternative energy, with the main emphasis on unicellular algae. Particular attention is paid to the use of phototrophs for generating electricity using biofuel cells (plant and enzymatic biofuel cells are discussed). This study focuses on microbial fuel cells (MFC), which, along with electric power, allow obtaining biofuels and biohydrogen. This article explains the factors limiting the MFC power, and ways of overcoming them. For example, it seems promising to develop various photobioreactors in order to reduce the loss of MFC power due to overvoltage. The use of microphototrophs in MFC has led to the development of photosynthetic MFC (or PhotoMFC) through the design of autotrophic photobioreactors with forced illumination. They allow generating oxygen through photosynthesis, both in situ and ex situ, by recirculating oxygen from the photobioreactor to the cathode chamber. Artificial redox mediators can be used here, transferring electrons directly from the non-catalytic cathode to O2, formed as a result of the photosynthetic activity of algae. Biologically catalyzed cathodes have been proven to generate less power than chemical catalysts. It is noted, that the MFC installations with the micro-algae allow utilizing a wider circle of different connections – the components of effluents and withdrawals: organic acids, sugar, alcohols, fats and other substrata. The use of phototrophs for the production of biofuels is of special interest. Several different types of renewable biofuels can be produced from microalgae, the production of which can be combined with wastewater treatment, CO2 capture and production of various compounds.
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