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A new approach to formulate the design of chemical reactors with multiple reactions is presented.
Some experimental results are reported and the suitability of these reactors for rapid multiple reactions is discussed.
More often than not, the activation/inhibition of multiple reactions is necessary to produce a predicted change for improvement of cellular properties or states.
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The main concepts involved and computation of the runaway boundaries for multiple reactions are illustrated by discussing three specific examples of consecutive, simultaneous and consecutive-simultaneous reactions.
Our approximate solution of what we have called the Tocher conundrum - what is the rate of etching of a surface when multiple reactions are necessary to remove its components - is given by the relation in (3.24), v p = ( ∑ j f j A j ) − 1. (5.1).
Sequence data from multiple reactions were analyzed with version 10.1 of the Genetics Computer Group Package (Accelrys, San Diego, CA, USA).
The contained reactions are often bundled (multiple reactions are summarized as one) or miss some reaction participants.
P. falciparum possesses a pathway to synthesize pyrimidine nucleotides de novo of which multiple reactions are predicted to be essential.
Sequence data from multiple reactions were analyzed by using version 10.1 of the Genetics Computer Group Package (Accelrys, San Diego, CA, USA).
Where this is not the case, alternative essential metabolic pathways consisting of multiple reactions are responsible, but such pathways are not common.
Similarly, multiple reactions are deemed to have flux dependency if all their reactants originate from one reaction already in the group.
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