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Evolution direction

Metal-loaded Ti02 particles are often used as photocatalysts. In most cases, the loaded metal acts as a catalyst for a reductive reaction such as hydrogen evolution. Direct measurements of the potential of the loaded metal, however, revealed that the metal can act not only as a catalyst for a reductive reaction but also as a catalyst for an oxidative reaction such as oxygen evolution under the... [Pg.40]

In most practical applications, one needs to know the free energy difference between two states, reactants and products or reactants and transition state, for instance. This magnitude provides the evolution direction for P and T constant. In ASEP/MD the standard free energy difference between the initial and final state in solution is approximated as... [Pg.588]

Applied molecular evolution, directed evolution, molecular breeding—the process is known by different names—all use some variation... [Pg.448]

A rich source of potential industrial biocatalysts, the heme enzymes are also a superb testing ground for laboratory evolution. Directed evolution approaches are already generating customized heme enzymes and probing the limits of heme enzyme catalysis. Over the next few years, these same approaches will allow us to explore the interconversion of function among different protein scaffolds and thereby observe how the protein modulates heme chemistry and how new functions are acquired. [Pg.238]

Differences in the size and coding capacity of mtDNA from various organisms most likely reflect the movement of DNA between mitochondria and the nucleus during evolution. Direct evidence for this movement comes from the observation that several proteins encoded by mtDNA in some species are encoded by nuclear DNA In others. It thus appears that entire genes moved from the mitochondrion to the nucleus, or vice versa, during evolution. [Pg.440]

The system of partial differential equations of first order, Eqs. (44), usually has to be treated as an initial-boundary-value problem on an appropriate energy region 0 < U < U°° and for times t > 0, where the time represents the evolution direction of the kinetic problem. Initial values for each of the distributions fo(U, i) and/,( /, t), suitable for the problem under consideration, have to be fixed, for example at t = 0. Appropriate boundary conditions for the system are given by the requirements /o([7 > U°°, t) = 0 and /,(0, t) = 0. [Pg.48]

Directed evolution proved to be a rapid yet powerful method to alter enzyme properties or to develop enzymes with novel properties, without requiring knowledge of the enzyme structure and catalytic mechanism. Arnold (2001) has an impressive review on enzyme performance improvement by a combination of rational design and directed evolution. Directed evolution applied to lipases has been reviewed by different authors (Petrounia and Arnold 2000 Tobin et al. 2000 Jaeger et al. 2001). Directed evolution has been employed for the creation of... [Pg.301]

Another unique application of ion irradiation is the in situ observation of microstructural evolution using a TEM combined with a connected accelerator (e.g. Ishino et al., 1983). This technique allows observation of microstructural evolution directly during ion irradiation by injecting ions with energies in the order of lOkeV to lOMeV into a thin-foil sample in a TEM. This method provides information about interactions of dislocations and cascades under ion irradiation. Continuous observations over time permit lifetime measurements of each cascade-induced vacancy cluster elucidating the nucleation and growth of the clusters under cascade damage (Ishino et a/.,1986). [Pg.191]

At a high temperature (300 °C), changing of the intrinsic viscosity s evolution direction takes place even in the absence of inhibitor, starting from low shear rates. [Pg.93]

Somehow the influences of POL and H are reversed relative to the prescription by trial succession of Eq. (3.250), revealing hydrophobicity as the main influential factor. However, due to the fact that the predicted activities of POL in Table 3.27 are all in the opposite evolution direction with respect to the activities recorded in Table 3.21, i.e., they are all negative, the uni-parametric tests and their associated hierarchy (3.256) are discarded, and one looks toward the second class of QSAR and catastrophe algorithms. [Pg.360]


See other pages where Evolution direction is mentioned: [Pg.150]    [Pg.248]    [Pg.249]    [Pg.105]    [Pg.1045]    [Pg.199]    [Pg.121]    [Pg.103]    [Pg.126]    [Pg.5]    [Pg.1854]    [Pg.155]    [Pg.474]    [Pg.63]    [Pg.65]    [Pg.320]    [Pg.26]    [Pg.231]    [Pg.141]    [Pg.1947]    [Pg.287]    [Pg.705]    [Pg.116]    [Pg.242]    [Pg.574]   
See also in sourсe #XX -- [ Pg.389 , Pg.390 , Pg.427 ]




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Accelerating Diagnostic Product Development Process with Molecular Rational Design and Directed Evolution

Applications of Directed Evolution

Applications of Recombinant DNA Technology Directed Evolution

Biocatalysis directed evolution

Biocatalyst directed evolution techniques

Chemical evolution directed

Cytochrome directed evolution

DERA by Directed Evolution

Design of Modern Biopharmaceuticals by Ultra-high-throughput Screening and Directed Evolution

Desymmetrization Directed evolution

Direct mapping, evolution equations

Directed Evolution - Enzyme Tuning Toward Higher Selectivity

Directed Evolution Fundamentals

Directed Evolution and Enzyme Libraries

Directed Evolution and Genetic Engineering of EHs

Directed Evolution as a Means to Engineer Enantioselective Enzymes

Directed Evolution of AMDase to an Artificial Profen Racemase

Directed Evolution of Biopharmaceuticals

Directed Evolution of Galactose Oxidase

Directed Evolution of Laccases

Directed Evolution of Medium-Redox Potential Laccases

Directed enzyme evolution

Directed evolution

Directed evolution

Directed evolution description

Directed evolution experimental stages

Directed evolution gene mutagenesis methods

Directed evolution goals

Directed evolution method

Directed evolution of nucleic acids

Directed evolution of protein function

Directed evolution strategies

Directed evolution techniques

Directed evolution, enzyme performance

Directed evolution, protein engineering

Directed molecular evolution

Enzyme Engineering by Directed Evolution

Enzymes, enantioselective, directed evolution

Fitness modeling-directed evolution

Functional evolution equations, direct

Heme directed evolution (

Heme proteins direct evolution

Laccases directed evolution

Molecular breeding directed evolution

Mutagenesis directed evolution

Nucleic acids directed evolution

Peroxidase directed evolution

Phage Display for the Directed Evolution of Enzymes

Practical Approaches to the Directed Evolution of Polymerase Function Selection or Screening

Protein Engineering by Directed Evolution

Protein activity, directed evolution

Protein design directed evolution

Protein stability directed evolution

Proteins directed evolution

Pseudomonas aeruginosa lipase, directed evolution

Rational Design and Directed Evolution

Recombination modeling-directed evolution

Screening of Large Libraries and Directed Enzyme Evolution

Specificity directed evolution

StEP in Directed Evolution

Structural Studies of Enzyme Directed Evolution

Temperature directed evolution

Transaminases directed evolution

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