163 research outputs found
Influence of sulphide Cu (I) promoting additives concentration on acid and catalytic properties of high-silica zeolites in straight-run gasoline conversion
In present article the influence of Cu[2]S promoting additives concentration on acid and catalytic properties of high silica MFI-type zeolites is investigated in the process of conversion of straight-run gasoline fractions of gas condensate into high octane components of motor fuels. It was shown that zeolite modified with 1% of Cu[2]S nanoscaled powder possesses the highest acid centers concentration and highest catalytic activity
Salvador Dali and jewellery design
The history of design is an important aspect for considering the heritage of individual members of this activity. The term βartβ is partly formulated from the assumption, that theexistence of this phenomenon is seen in the temporary space.Rethinking the aesthetic perception of the world, as an individual artist and as the creative discoveries and the era of the arts in general is made by literary translation. One of the brightest occasions in the history of design in 20 century was the appearance of the Spanish artist, painter, graphic artist, sculptor, director, writer and designer, Salvador Dali.The cultural situation of the 20th century as well as considering surrealismto be a special phenomenon in the development of Europeanculture cause the interest to historians and theorists of culture
Π Π°Π·ΡΠ°Π±ΠΎΡΠΊΠ° Π°Π²ΡΠΎΠΌΠ°ΡΠΈΠ·ΠΈΡΠΎΠ²Π°Π½Π½ΠΎΠΉ ΡΠΈΡΡΠ΅ΠΌΡ ΡΠΏΡΠ°Π²Π»Π΅Π½ΠΈΡ ΠΏΠ΅ΡΠΈ ΠΏΠΎΠ΄ΠΎΠ³ΡΠ΅Π²Π° ΡΡΡΠΎΠΉ Π½Π΅ΡΡΠΈ ΡΡΡΠ°Π½ΠΎΠ²ΠΊΠΈ ΠΏΠΎΠ΄Π³ΠΎΡΠΎΠ²ΠΊΠΈ Π½Π΅ΡΡΠΈ
Π Π°Π·ΡΠ°Π±ΠΎΡΠΊΠ° Π°Π²ΡΠΎΠΌΠ°ΡΠΈΠ·ΠΈΡΠΎΠ²Π°Π½Π½ΠΎΠΉ ΡΠΈΡΡΠ΅ΠΌΡ ΡΠΏΡΠ°Π²Π»Π΅Π½ΠΈΡ ΠΏΠ΅ΡΠΈ ΠΏΠΎΠ΄ΠΎΠ³ΡΠ΅Π²Π° ΡΡΡΠΎΠΉ Π½Π΅ΡΡΠΈ ΡΡΡΠ°Π½ΠΎΠ²ΠΊΠΈ ΠΏΠΎΠ΄Π³ΠΎΡΠΎΠ²ΠΊΠΈ Π½Π΅ΡΡΠΈ, ΠΊΠΎΡΠΎΡΠ°Ρ ΠΏΠΎΠ·Π²ΠΎΠ»ΠΈΡ ΡΠ»ΡΡΡΠΈΡΡ ΠΊΠ°ΡΠ΅ΡΡΠ²Π΅Π½Π½ΡΠ΅ ΠΏΠΎΠΊΠ°Π·Π°ΡΠ΅Π»ΠΈ ΡΡΡΠΎΠΉ Π½Π΅ΡΡΠΈ Π΄Π»Ρ Π΄Π°Π»ΡΠ½Π΅ΠΉΡΠ΅ΠΉ ΠΏΠ΅ΡΠ΅ΡΠ°Π±ΠΎΡΠΊΠΈ Π² ΡΠΎΠ²Π°ΡΠ½ΡΡ Π½Π΅ΡΡΡDevelopment of an automated control system for the furnace for heating crude oil of an oil preparation unit, which will improve the quality indicators of crude oil for further processing into commercial oi
Time-resolved generation of membrane potential by ba3 cytochrome c oxidase from Thermus thermophilus coupled to single electron injection into the O and OH states
peer-reviewedTwo electrogenic phases with characteristic times of ~ 14 ΞΌs and ~ 290 ΞΌs are resolved in the kinetics of membrane potential generation coupled to single-electron reduction of the oxidized βrelaxedβ O state of ba3 oxidase from T. thermophilus (O β E transition). The rapid phase reflects electron redistribution between CuA and heme b. The slow phase includes electron redistribution from both CuA and heme b to heme a3, and electrogenic proton transfer coupled to reduction of heme a3. The distance of proton translocation corresponds to uptake of a proton from the inner water phase into the binuclear center where heme a3 is reduced, but there is no proton pumping and no reduction of CuB. Single-electron reduction of the oxidized βunrelaxedβ state (OH β EH transition) is accompanied by electrogenic reduction of the heme b/heme a3 pair by CuA in a βfastβ phase (~ 22 ΞΌs) and transfer of protons in βmiddleβ and βslowβ electrogenic phases (~ 0.185 ms and ~ 0.78 ms) coupled to electron redistribution from the heme b/heme a3 pair to the CuB site. The βmiddleβ and βslowβ electrogenic phases seem to be associated with transfer of protons to the proton-loading site (PLS) of the proton pump, but when all injected electrons reach CuB the electronic charge appears to be compensated by back-leakage of the protons from the PLS into the binuclear site. Thus proton pumping occurs only to the extent of ~ 0.1 H+/eβ, probably due to the formed membrane potential in the experiment.ACCEPTEDpeer-reviewe
Specific inhibition of proton pumping by the T315V mutation in the K channel of cytochrome ba3 from Thermus thermophilus
Cytochrome ba3 from Thermus thermophilus belongs to the B family of hemeβcopper oxidases and pumps protons across the membrane with an as yet unknown mechanism. The K channel of the A family hemeβcopper oxidases provides delivery of a substrate proton from the internal water phase to the binuclear hemeβcopper centre (BNC) during the reductive phase of the catalytic cycle, while the D channel is responsible for transferring both substrate and pumped protons. By contrast, in the B family oxidases there is no D-channel and the structural equivalent of the K channel seems to be responsible for the transfer of both categories of protons. Here we have studied the effect of the T315V substitution in the K channel on the kinetics of membrane potential generation coupled to the oxidative half-reaction of the catalytic cycle of cytochrome ba3. The results suggest that the mutated enzyme does not pump protons during the reaction of the fully reduced form with molecular oxygen in a single turnover. Specific inhibition of proton pumping in the T315V mutant appears to be a consequence of inability to provide rapid (Οβ―~β―100β―ΞΌs) reprotonation of the internal transient proton donor(s) of the K channel. In contrast to the A family, the K channel of the B-type oxidases is necessary for the electrogenic transfer of both pumped and substrate protons during the oxidative half-reaction of the catalytic cycle.Peer reviewe
ΠΡΠ΅Π½ΠΊΠ° Π³ΠΈΠ΄ΡΠΎΠ³Π΅ΠΎΠ΄ΠΈΠ½Π°ΠΌΠΈΡΠ΅ΡΠΊΠΎΠ³ΠΎ Π²Π»ΠΈΡΠ½ΠΈΡ ΡΠ΅ΠΆΠΈΠΌΠ° ΡΠΊΡΠΏΠ»ΡΠ°ΡΠ°ΡΠΈΠΈ ΡΠΊΠ²Π°ΠΆΠΈΠ½ Π½Π° ΠΎΡΠ½ΠΎΠ²Π΅ ΡΡΠ°ΡΠΈΡΡΠΈΡΠ΅ΡΠΊΠΈΡ ΡΡΠ½ΠΊΡΠΈΠΉ
ΠΡΡΠ»Π΅Π΄ΠΎΠ²Π°Π½ΠΎ Π²ΠΎΠ·Π΄Π΅ΠΉΡΡΠ²ΠΈΠ΅ ΡΠ°Π±ΠΎΡΡ ΡΠΊΡΠΏΠ»ΡΠ°ΡΠ°ΡΠΈΠΎΠ½Π½ΡΡ
ΡΠΊΠ²Π°ΠΆΠΈΠ½ ΠΏΠΎΠ»ΠΈΠ³ΠΎΠ½Π° Π·Π°Ρ
ΠΎΡΠΎΠ½Π΅Π½ΠΈΡ ΠΏΡΠΎΠΌΡΡΠ»Π΅Π½Π½ΡΡ
ΠΎΡΡ
ΠΎΠ΄ΠΎΠ² Π‘ΠΈΠ±ΠΈΡΡΠΊΠΎΠ³ΠΎ Ρ
ΠΈΠΌΠΈΡΠ΅ΡΠΊΠΎΠ³ΠΎ ΠΊΠΎΠΌΠ±ΠΈΠ½Π°ΡΠ° Π½Π° ΠΊΠΎΠ»Π΅Π±Π°Π½ΠΈΠ΅ Π½Π°ΠΏΠΎΡΠΎΠ² Π² Π½Π°Π±Π»ΡΠ΄Π°ΡΠ΅Π»ΡΠ½ΡΡ
ΡΠΊΠ²Π°ΠΆΠΈΠ½Π°Ρ
ΠΈ Π²ΡΠ΄Π΅Π»Π΅Π½ΠΈΠ΅ ΡΠ°ΡΡΠΎΡΠ½ΡΡ
ΡΠΎΡΡΠ°Π²Π»ΡΡΡΠΈΡ
ΡΠ΅Ρ
Π½ΠΎΠ³Π΅Π½Π½ΠΎΠ³ΠΎ ΠΈ ΠΏΡΠΈΡΠΎΠ΄Π½ΠΎΠ³ΠΎ ΠΊΠΎΠ»Π΅Π±Π°Π½ΠΈΠΉ Π² ΡΠΏΠ΅ΠΊΡΡΠ΅. ΠΠΎΠΊΠ°Π·Π°Π½Π° Π²ΠΎΠ·ΠΌΠΎΠΆΠ½ΠΎΡΡΡ ΠΈΡΠΏΠΎΠ»ΡΠ·ΠΎΠ²Π°Π½ΠΈΡ ΡΡΠ½ΠΊΡΠΈΠΈ Π²Π·Π°ΠΈΠΌΠ½ΠΎΠΉ ΠΊΠΎΡΡΠ΅Π»ΡΡΠΈΠΈ ΠΈ Π€ΡΡΡΠ΅-Π°Π½Π°Π»ΠΈΠ·Π° Π΄Π»Ρ ΠΎΡΠ΅Π½ΠΊΠΈ Π³ΠΈΠ΄ΡΠΎΠ³Π΅ΠΎΠ΄ΠΈΠ½Π°ΠΌΠΈΡΠ΅ΡΠΊΠΎΠ³ΠΎ Π²Π»ΠΈΡΠ½ΠΈΡ ΡΠ΅ΠΆΠΈΠΌΠ° ΡΠ°Π±ΠΎΡΡ ΡΠΊΡΠΏΠ»ΡΠ°ΡΠ°ΡΠΈΠΎΠ½Π½ΡΡ
ΡΠΊΠ²Π°ΠΆΠΈΠ½
ΠΡΡ ΠΈΡΠ΅ΠΊΡΡΡΠ° ΠΏΡΠΎΠ³ΡΠ°ΠΌΠΌΠ½ΠΎΠ³ΠΎ ΡΡΠ΅Π΄ΡΡΠ²Π° Π΄Π»Ρ Π°Π½Π°Π»ΠΈΡΠΈΠΊΠΈ ΠΈ ΠΈΠ·ΡΠ°Π»ΠΈΠ·Π°ΡΠΈΠΈ ΠΏΠΎΠ²Π΅Π΄Π΅Π½ΠΈΡ ΠΏΠΎΠ»ΡΠ·ΠΎΠ²Π°ΡΠ΅Π»Π΅ΠΉ
AbstractThe ba3-type cytochrome-c oxidase from Thermus thermophilus has been crystallized in its native form. Crystallization was achieved by the batch and the vapour diffusion sitting drop methods using polyethylene glycol monomethyl ether 2000 as precipitating agent in the presence of octyl-Ξ²-d-thioglucoside as detergent. The crystals diffract to 3.8 Γ
, belong to the space group P2 or P21 and have unit cell dimensions of a = 80.7 AΜ; b = 116.0 AΜ; c = 156.9 AΜ and Ξ² = 104.4Β°. The asymmetric unit contains two ba3-type oxidase molecules
Exploring the cytochrome c folding mechanism: cytochrome c552 from thermus thermophilus folds through an on-pathway intermediate.
Understanding the role of partially folded intermediate states in the folding mechanism of a protein is a crucial yet very difficult problem. We exploited a kinetic approach to demonstrate that a transient intermediate of a thermostable member of the widely studied cytochrome c family (cytochrome c552 from Thermus thermophilus) is indeed on-pathway. This is the first clear indication of an obligatory intermediate in the folding mechanism of a cytochrome c. The fluorescence properties of this intermediate demonstrate that the relative position of the heme and of the only tryptophan residue cannot correspond to their native orientation. Based on an analysis of the three-dimensional structure of cytochrome c552, we propose an interpretation of the data which explains the residual fluorescence of the intermediate and is consistent with the established role played by some conserved interhelical interactions in the folding of other members of this family. A limited set of topologically conserved contacts may guide the folding of evolutionary distant cytochromes c through the same partially structured state, which, however, can play different kinetic roles, acting either as an intermediate or a transition state
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