TLS Online TPP Program

#Question id: 19486


The growth of S.cerevisiae on glucose under anaerobic conditions can be described by the following reaction:
C6H12O6 + aNH3 → 0.59 CH1.64N0.16O0.52 (biomass) + 0.43 C3H8O3 + 1.54CO2 + 1.3C2H5OH + 0.036H2
and determine the product yield coefficient Y etoh/s and determine coefficient a.

#Section 4: Fundamentals of Biological Engineering
  1. 0.57 g. g⁻¹, 0.078
  2. 0.33 g. g⁻¹, 0.094
  3. 0.45 g. g⁻¹, 0.086
  4. 0.44 g. g⁻¹, 0.056
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TLS Online TPP Program

#Question id: 13071

#Section 7: Recombinant DNA technology and Other Tools in Biotechnology

Modifications of the agglutination reaction involve the use of ________particles, which allow the reaction to be observed more easily in the liquid phase

TLS Online TPP Program

#Question id: 13072

#Section 7: Recombinant DNA technology and Other Tools in Biotechnology

Inheritance pattern of RFLP and RAPD markers for genome mapping in plants;

TLS Online TPP Program

#Question id: 13073

#Section 7: Recombinant DNA technology and Other Tools in Biotechnology

Restriction enzymes must be use in RFLP and RAPD markers for genome mapping in plants;

TLS Online TPP Program

#Question id: 13074

#Section 7: Recombinant DNA technology and Other Tools in Biotechnology

Type of probe used in RFLP;

TLS Online TPP Program

#Question id: 13075

#Section 7: Recombinant DNA technology and Other Tools in Biotechnology

Radioisotopes must be used in RFLP and RAPD markers

TLS Online TPP Program

#Question id: 13076

#Section 7: Recombinant DNA technology and Other Tools in Biotechnology

Restriction fragment length polymorphism denotes that a single restriction enzyme produces fragments of different lengths from the same stretch of genomic DNA of different strains of a species or from different related species. RFLPs are detected as follows:

i.  Large molecular weight genomic DNA is isolated from several strains or related species;

ii.  The fragments in these digests are separated through electrophoresis

iii.  These 'DNAs are then digested with a selected restriction enzyme

iv.  Exposed to a suitably radio-labelled appropriate DNA probe under conditions favouring DNA: DNA hybridization

v.  The resulting gel lanes are transferred and fixed to a suitable solid support and

vi.   The free probes are removed

vii.  The fragments to which the probe has hybridized are detected by filming them as distinct bands on a suitable photofilm through autoradiography.