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#Question id: 13102


 With the help of DNA fingerprinting which can be used to determine paternity. There are three babies (Baby A, Baby B and Baby C) in a maternity ward, and three sets of confused and worried parents. (Father and Mother #1 are a couple, as are Father and Mother #2, and Father and Mother #3.) 
You do each PCR reaction and load each one into a separate well of an agarose gel, and then run the gel.
 

 Why is it that having more repeats leads to a band that is higher in the gel?

#SCPH06 I Botany
  1. Because they are homozygotes at this region
  2. The more repeats you have, the longer your DNA fragment is, and longer DNA fragments migrate more slowly in gels.
  3. Because they are heterozygotes at this region
  4. The less no. of repeats you have, the longer your DNA fragment is, and longer DNA fragments migrate more slowly in gels.
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TLS Online TPP Program

#Question id: 14300

#SCPH05 I 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

#SCPH05 I 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?

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TLS Online TPP Program

#Question id: 14302

#SCPH05 I 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?

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TLS Online TPP Program

#Question id: 14303

#SCPH05 I 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?

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TLS Online TPP Program

#Question id: 14304

#SCPH05 I 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 productivity at 0.8 Dmax?

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TLS Online TPP Program

#Question id: 14305

#SCPH05 I Biotechnology

Ethanol is to be used as a substrate for single-cell protein production in a chemostat. The available equipment can achieve an oxygen transfer rate of 10 g O2/l of liquid per hour. Assume the kinetics of cell growth on ethanol is of the Monod type, with µm = 0.5 h–1, Ks = 30 mg/l, YX/S = 0.5 cells/g ethanol, and YO2/S = 2 g O2/g EtOH. We wish to operate the chemostat with an ethanol concentration in the feed of 22 g/L. We also wish to maximize the biomass productivity and minimize the loss of unused ethanol in the effluent. Determine the required dilution rate

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