TLS Online TPP Program

#Question id: 3862


The largest gene characterized to date is:

#Part-A Aptitude & General Biotechnology
  1. 50,000 nt

  2. 500,000 nt  

  3. 1,000,000 nt

  4. 2,500,000 nt

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TLS Online TPP Program

#Question id: 10250

#Part-B Specialized Branches in Biotechnology

Glycolysis involves a series of reactions catalyzed by enzymes located in,

TLS Online TPP Program

#Question id: 18706

#Part-A Aptitude & General Biotechnology

Sources of thermostable DNA polymerases with proofreading (3′–5′ exonuclease) activity are given match them correctly
DNA polymerase                          Source
a. Tma                                      i. Thermotoga maritima
b. Deep vent tm                      ii. Pyrococcus furiosus
c. Tli                                      iii. Thermococcus litoralis
d. Pfu                                      iv.  Pyrococcus sp
e. Pwo                                      v. Pyrococcus woesi

TLS Online TPP Program

#Question id: 18602

#Part-A Aptitude & General Biotechnology

Suppose a unbiased die is thrown 72 times and getting a 4 on a throw is termed as success then find the variance of number of success ?

TLS Online TPP Program

#Question id: 882

#Part-B Specialized Branches in Biotechnology

Choose correct statements about thermophilic proteins

I. The proteins found in thermophilic species are much more stable than their mesophilic counterparts.

II. All thermostable proteins have such a high incidence of salt bridges

III. the most important of which are an increased size of the protein’s hydrophobic core, an increased size of the interface between its domains and/or subunits, and a more tightly packed core as evidenced by a reduced surface-to-volume ratio.

IV. Several of these thermostable enzymes have a superabundance of salt bridges on their surfaces.

TLS Online TPP Program

#Question id: 18847

#Part-A Aptitude & General Biotechnology

You know that the protein you want to purify from a natural source forms a multimer with multiple sub-units giving a molecular weight in solution much bigger than visualised denatured on SDS-PAGE. There is only a small amount of the target protein in the total protein sample. Which of the following is an appropriate purification strategy?