TLS Online TPP Program

#Question id: 597


The Km values for enzyme reactions such as A + B → C + D

#Section 2: General Biology
  1. cannot be determined using the Lineweaver-Burk plot analysis.

  2. can be determined by holding one (A or B) at high concentration, while varying the concentration of the other substrate.

  3. can be determined for one substrate and not the other.

  4. do not indicate the efficiency of the enzyme.

More Questions
TLS Online TPP Program

#Question id: 14300

#Section 5: Bioprocess Engineering and Process Biotechnology

A 15-m 3 chemostat is operated with dilution rate 0.1 h-1. A continuous steriliser with steam injection and flash cooling delivers sterilized medium to the fermenter. Medium in the holding section of the steriliser is maintained at 130⁰C The concentration of contaminants in the raw medium is 105 ml-l; an acceptable contamination risk is one organism every 3 months. The Arrhenius constant and activation energy for thermal death are estimated to be 7.5 × 1039 h-1 and 288.5 kJ gmol- 1, respectively. The steriliser pipe inner diameter is 12 cm. At 130⁰C the liquid density is 1000 kg m- 3 and the viscosity is 4 kg m- 1 h- 1. Assuming perfect plug flow, determine the length of the holding section.   __________________

TLS Online TPP Program

#Question id: 14301

#Section 5: Bioprocess Engineering and Process Biotechnology

Pseudomonas sp. has a mass doubling time of 2.4 h when grown on acetate. The saturation constant using this substrate is 1.3 g/l (which is unusually high), and cell yield on acetate is 0.46 g cell/g acetate. If we operate a chemostat on a feed stream containing 38 g/l acetate, find the Cell concentration when the dilution rate is one-half of the maximum?

                ___________________                                          

TLS Online TPP Program

#Question id: 14302

#Section 5: Bioprocess Engineering and Process Biotechnology

Pseudomonas sp. has a mass doubling time of 2.4 h when grown on acetate. The saturation constant using this substrate is 1.3 g/l (which is unusually high), and cell yield on acetate is 0.46 g cell/g acetate. If we operate a chemostat on a feed stream containing 38 g/l acetate, find the Substrate concentration when the dilution rate is 0.8Dmax?

                        __________________                                      

TLS Online TPP Program

#Question id: 14303

#Section 5: Bioprocess Engineering and Process Biotechnology

Pseudomonas sp. has a mass doubling time of 2.4 h when grown on acetate. The saturation constant using this substrate is 1.3 g/l (which is unusually high), and cell yield on acetate is 0.46 g cell/g acetate. If we operate a chemostat on a feed stream containing 38 g/l acetate, find the Maximum dilution rate?

_________