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Ławniczak Łukasz Kaczorek Ewa Olszanowski Andrzej 《World journal of microbiology & biotechnology》2011,27(5):1183-1188
Recent biodegradation researches are focused on improving the deterioration efficiency and maintaining the stability of microbial
activity during the process. Immobilizing bacterial cells by using the adhesive method is a simple way to achieve both objectives.
The purpose of this study was to evaluate how the immobilization of bacterial cells by the biofilm forming method influences
the biodegradation efficiency of two different bacterial consortia—low diesel oil degraders (base deterioration efficiency < 40%)
and high phenol degraders (base deterioration efficiency > 90%). The degradation tests were carried out on four different
carriers (expanded clay pellets, polypropylene, polyvinyl chloride rings and paperboard). The obtained results show that biofilms
may considerably increase the efficiency of low degraders. The best diesel oil deterioration (80%) was achieved when paperboard
was used as a carrier. However, the immobilization of high degraders did not significantly influence their base biodegradation
potential. A 6% increase was noted only for the expanded clay pellets. 相似文献
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Amphotericin B (AmB)--a polyene macrolide antibiotic--exhibits strong antifungal activity, however, is known to be very toxic to mammalian cells. In order to decrease AmB toxicity, a number of its derivatives have been synthesized. Basing on in vitro and in vivo research, it was evidenced that one of AmB derivatives, namely N-methyl-N-D-fructopyranosylamphotericin B methyl ester (in short MF-AME) retained most of the antifungal activity of the parent antibiotic, however, exhibited dramatically lower animal toxicity. Therefore, MF-AME seems to be a very promising modification product of AmB. However, further development of this derivative as potential new antifungal drug requires the elucidation of its molecular mechanism of reduced toxicity, which was the aim of the present investigations. Our studies were based on examining the binding energies by determining the strength of interaction between MF-AME and membrane sterols (ergosterol-fungi sterol, and cholesterol-mammalian sterol) and DPPC (model membrane phospholipid) using the Langmuir monolayer technique, which serves as a model of cellular membrane. Our results revealed that at low concentration the affinity of MF-AME to ergosterol is considerably stronger as compared to cholesterol, which correlates with the improved selective toxicity of this drug. It is of importance that the presence of phospholipids is essential since--due to very strong interactions between MF-AME and DPPC--the antibiotic used in higher concentration is "immobilized" by DPPC molecules, which reduces the concentration of free antibiotic, thus enabling it to selectively interact with both sterols. 相似文献
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Hamada H Kameshima N Szymańska A Wegner K Lankiewicz Ł Shinohara H Taki M Sisido M 《Bioorganic & medicinal chemistry》2005,13(10):3379-3384
A new fluorescent amino acid, L-2-acridonylalanine, was incorporated into proteins at specific positions using 4-base codon/anticodon strategy. The efficiency of the incorporation was high enough to obtain enough quantities of the mutants. The acridonyl group was highly fluorescent when it was excited at the wavelengths of blue-lasers and was highly photodurable compared with conventional fluorophores often used for biological analyses. The fluorescence intensity was sensitive to small changes in the polarity of the environment. When the nonnatural amino acid was incorporated into specific positions of streptavidin, the mutant protein worked as a fluorescent sensor to biotin. Similarly, when the amino acid was incorporated into camel single-chain antibody, the mutant protein sensitively responded to the antigen molecule. The high incorporation efficiency, the high photodurability, the excitability with blue-lasers, and high sensitivity to the environment make the acridonylalanine as the promising fluorescent amino acid for sensing small molecules when incorporated into specific positions of various antibodies, receptors, and enzymes. 相似文献
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