A culture of bacteria is infected with bacteriophage at a multiplicity of 0.3. The probability of a single cell infected with 3 phages is
(A) 0.009
(B) 0.027
(C) 0.9
(D) 0.27
Questions and Answers
Interferon-β is produced by (A) bacteria infected cells (B) virus infected cells (C) both virus and bacteria infected cells (D) fungi infected cells
Interferon-β is produced by
(A) bacteria infected cells
(B) virus infected cells
(C) both virus and bacteria infected cells
(D) fungi infected cells
Which one of the following DOES NOT belong to the domain of Bacteria? (A) Cyanobacteria (B) Proteobacteria (C) Bacteroids (D) Methanobacterium
Which one of the following DOES NOT belong to the domain of Bacteria?
(A) Cyanobacteria
(B) Proteobacteria
(C) Bacteroids
(D) Methanobacterium
An example for template-independent DNA polymerase is (A) DNA Polymerase I (B) RNA polymerase (C) Terminal deoxynucleotidyl transferase (D) DNA polymerase III
An example for template-independent DNA polymerase is
(A) DNA Polymerase I
(B) RNA polymerase
(C) Terminal deoxynucleotidyl transferase
(D) DNA polymerase III
Q.9 Under stress conditions bacteria accumulate (A) ppGpp (Guanosine tetraphosphate) (B) pppGpp (Guanosine pentaphosphate) (C) both ppGpp and pppGpp (D) either ppGpp or pppGpp
Q.9 Under stress conditions bacteria accumulate
(A) ppGpp (Guanosine tetraphosphate)
(B) pppGpp (Guanosine pentaphosphate)
(C) both ppGpp and pppGpp
(D) either ppGpp or pppGpp
Q.8 During transcription (A) DNA Gyrase introduces negative supercoils and DNA Topoisomerase I removes negative supercoils (B) DNA Topoisomerase I introduces negative supercoils and DNA Gyrase removes negative supercoils (C) both DNA Gyrase and DNA Topoisomerase I introduce negative supercoils (D) both DNA Gyrase and DNA Topoisomerase I remove negative supercoils
Q.8 During transcription
(A) DNA Gyrase introduces negative supercoils and DNA Topoisomerase I removes negative supercoils
(B) DNA Topoisomerase I introduces negative supercoils and DNA Gyrase removes negative supercoils
(C) both DNA Gyrase and DNA Topoisomerase I introduce negative supercoils
(D) both DNA Gyrase and DNA Topoisomerase I remove negative supercoils
Q.7 In transgenics, alterations in the sequence of nucleotide in genes are due to P. Substitution Q. Deletion R. Insertion S. Rearrangement (A) P and Q (B) P, Q and R (C) Q and R (D) R and S
Q.7 In transgenics, alterations in the sequence of nucleotide in genes are due to
P. Substitution
Q. Deletion
R. Insertion
S. Rearrangement
(A) P and Q
(B) P, Q and R
(C) Q and R
(D) R and S
Q.6 Peptidyl transferase activity resides in (A) 16S rRNA (B) 23S rRNA (C) 5S rRNA (D) 28S rRNA
Q.6 Peptidyl transferase activity resides in
(A) 16S rRNA
(B) 23S rRNA
(C) 5S rRNA
(D) 28S rRNA
Q.5 Program used for essentially local similarity search is (A) BLAST (B) RasMol (C) ExPASY (D) SWISS-PROT
Q.5 Program used for essentially local similarity search is
(A) BLAST
(B) RasMol
(C) ExPASY
(D) SWISS-PROT
Q.4 Antibiotic resistance marker that CANNOT be used in a cloning vector in Gram negative bacteria is (A) Streptomycin (B) Ampicillin (C) Vancomycin (D) Kanamycin
Q.4 Antibiotic resistance marker that CANNOT be used in a cloning vector in Gram negative bacteria is
(A) Streptomycin
(B) Ampicillin
(C) Vancomycin
(D) Kanamycin