1. The protein target for rifampin is DNA dependent RNA polymerase. Rifampin binds to the subunit of RNA polymerase and inhibits its activity.
Rifampin is an antibiotic mostly used in the treatment of tuberculosis.
Rifampin inhibits the process of Transcription there by preventing RNA synthesis.
2. As we know , in RNA Thymine will be replaced with Uracil , the new mRNA codons will be
5' AGC 3' becomes UCG
5' ATC 3' becomes UAG
3. Point mutation has occured because a single base is replaced by another base .
4. Before mutation the codon coded for SERINE ( UCG ) and after mutation it coded for a STOP CODON ( UAG).
The strain of XDR-TB that the young man had above was studied further by analyzing the...
The strain of XDR-TB that the young man had above was studied further by analyzing the DNA of the Mycobacterium tuberculosis. The investigators particularly looked at the gene for the protein targeted by the antibiotic rifampin. MDR-TB and XDR-TB are resistant to rifampin. Q1. What is the protein target for rifampin in the bacterial cells? What biological process does the antibiotic stop? (see notes). The following results were obtained from the young man's M. tuberculosis for the DNA sequence of...
i think it might be Glutamate, but im not sure. Someone please help!! its the last question i need to finish this mindtap. please respond quickly too, its due TODAY at 11:59pm EST CENGAGE MINDTAP a se Chapter 9 Digging Deeper Conceptual Learning Activity Second base U C A G UUU Phenylalanine UCU UUC Phenylalanine UCC Leucine UCA Leucine UCG Leucine CCU Leucine CCC Leucine CCA Leucine CCG Isoleucine ACU Isoleucine ACC Isoleucine ACA Methionine ACG Cysteine U Cysteine C...
A mutation is a permanent change in the sequence of nucleotide bases in a cell's DNA. Most mutations happen during DNA replication, but their effects are not seen until transcription and translation. Even a small mutation that changes a single nucleotide can have a major impact on the resulting proteins that are made in the cell. с The table following the amino acid chart lists a segment of a normal gene. Type in the corresponding mRNA strand and the amino...
Sickle-cell Anemia Study Sickle-cell anemia or Sickle-cell disease, is a hereditary disorder. characterized by aryabnormality in the oxygen-carrying hemoglobin molecule in erythrocytes. Sickle-cell conditions have an autosomal recessive pattern of inheritance from parents. The sickle cell defect is a mutation of a single nucleotide of the hemoglobin B gene, which results in glutamic acid being substituted by a different amino acid at position 6. Hemoglobin with this mutation is referred to as Hbs, as opposed to the normal hemoglobin HbA....