TLS Online TPP Program

#Question id: 4510


Which statements are true about group I and group II introns,

A. Group I (and II) introns are not enzymes because they have a turnover number of only 1.

B. A third transesterification reaction can occur to cyclize the intron.

C. They cannot be readily converted into ribozymes.

D. It is similar to the way that the self-cleaving Hammerhead could be converted to a ribozyme by separating the active site from the substrate

#Unit 3. Fundamental Processes
  1. A, B and D

  2. B, C and D

  3. C and D only

  4. A, B, C and D

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#Question id: 226

#Unit 1. Molecules and their Interaction Relevant to Biology

Which in not a lipid-soluble vitamin?

TLS Online TPP Program

#Question id: 10139

#Unit 6. System Physiology – Plant

There are two distinct forms of rubisco. Form I is found in vascular plants, algae, and cyanobacteria; form II is confined to certain photosynthetic bacteria, Some statements about the Rubisco is given;
a.) A complex form I structure with eight identical large subunits each containing a catalytic site, and eight identical small subunits of uncertain function
b.) The form II rubisco of photosynthetic bacteria is simpler in structure, having two subunits that in many respects resemble the large subunits of the plant enzyme
c.) The plant enzyme has an exceptionally low turnover number; only three molecules of CO2 are fixed per second per molecule of rubisco at 25 o C
d.) Rubisco makes up almost 50% of soluble protein in chloroplasts and is probably one of the most abundant enzymes in the biosphere
Which of the following statements about rubisco will true?

TLS Online TPP Program

#Question id: 1590

#Unit 4. Cell Communication and Cell Signaling

An epitope associates with which part of an antibody?

TLS Online TPP Program

#Question id: 5778

#Unit 8. Inheritance Biology

DNA is repaired by ____ in which a pyrimidine dimer is split

TLS Online TPP Program

#Question id: 31359

#Unit 13. Methods in Biology

Which of the following microscopy uses photoswitchable fluorophores that can be switched between a "on" (fluorescent) and "off" (dark) state, allowing only a small subset of molecules to be illuminated at a time, enabling precise localization of each individual molecule.