Download Biotransformation And Bioprocesses by Mukesh Doble PDF

By Mukesh Doble

ISBN-10: 0824747755

ISBN-13: 9780824747756

From the laboratory to full-scale advertisement construction, this reference presents a transparent and in-depth research of bioreactor layout and operation and encompasses severe features of the biocatalytic production approach. It clarifies ideas in response and biochemical engineering, artificial and biotransformation chemistry, and biocell and enzyme kinetics for winning purposes of biocatalysis and bioprocess applied sciences within the meals, chiral drug, diet, pharmaceutical, and animal feed industries. learning reactions from small to supramolecules, this reference offers an considerable offer of end-of-chapter difficulties to sharpen realizing of key options awarded within the textual content.

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Extra resources for Biotransformation And Bioprocesses

Example text

The reactants of an enzyme-catalyzed reaction are called substrates. The catalysis takes place in a specific region of the enzyme, referred to as the active center or catalytic cavity. Most of the enzymes use a nonprotein component called a cofactor for bringing about this catalytic activity. The outstanding characteristic feature of enzyme catalysis is that the enzyme specifically binds its substrates and the reaction takes place in the confines of the enzyme-substrate complex. Thus, to understand how an enzyme works, we not only need to know the structure of the native enzyme, but also the structure of the complex of the enzyme with its substrate.

The average length is around three turns, corresponding to 10 residues. 5 A˚ along the helical axis, this corresponds to about 15 A˚ from one end to the other of an average a-helix. All the hydrogen bonds in an a-helix point in the same direction. So the peptide fraction has a net dipole moment aligned along the a-helical axis. Different side chains have been found to have weak but definite preferences either for or against being in ahelices. Thus, Ala(A), Glu(E), Leu(L) and Met(M) are good a-helix formers.

Molecules, like atoms or even the subatomic particles, are dynamic entities having a variety of movements at the ambient temperature and pressure conditions. Hence, when we mix CH3Cl and NaOH, the distorted electron cloud of the methyl chloride collides with the electron-rich (almost spherical) hydroxide ion electron cloud in infinite number of ways. The collision in which the electron cloud of the hydroxide ion comes close enough to the electron-deficient center (carbon) of the methyl chloride is the fruitful collision, leading to the product formation.

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