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These impacts of recycle could lead to significant necessary process modifications if enzyme recycling were to be implemented in an industrial process.
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There exist other possible contributions to these delays, such as post-translational modification of some enzymes or enzyme-to-enzyme interactions.
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Additionally, dietary modification and oral enzyme replacement trials using synthetic sucrase (sacrosidase) have been employed to determine if they can clinically alleviate symptoms of sucrase-isomaltase deficiency [22, 23].
This result is suggestive of a post-translational modification of the enzyme.
The NBS mediated modification of purified enzyme resulted in total loss of activity.
The M+305-Da peaks were not detected which indicated an oxidative modification of the enzyme.
Posttranslational modification of PFK1 enzyme might exhibit another important role in cancer metabolism.
However, significantly, the DNA gained sensitivity to cleavage by the Type III restriction-modification enzyme, EcoP15I.
PA0438, for example, is annotated as a restriction-modification enzyme "restriction enzyme alpha subunit".
Cysteine carbamidomethylation was selected as a fixed modification, and lysine and proline oxidation included as variable modifications, for all enzymes.
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