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Bacterial Physiology (Micr430)

This lecture delves into the key aspects of bacterial protein synthesis, also known as translation. It discusses the triplet code that defines amino acids, including the concept of degeneracy where multiple codes can specify a single amino acid. The structure and function of transfer RNA (tRNA) are explained, highlighting its role in matching codons on mRNA. Step-by-step processes of initiation, elongation, and termination of protein synthesis are covered, detailing the involvement of ribosomal subunits and initiation factors. This comprehensive overview is crucial for understanding macromolecular synthesis in bacteria.

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Bacterial Physiology (Micr430)

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  1. Bacterial Physiology (Micr430) Lecture 8 Macromolecular Synthesis and Processing: Proteins (Text Chapter: 10)

  2. PROTEIN SYNTHESIS • Also termed translation • A triplet code specifies for an amino acid • There may be more than one code for a particular amino acid (degeneracy) • Among 64 combinations of four bases, three (UAG, UAA and UGA) do not encode any amino acid - nonsense codons

  3. Transfer RNA • tRNA possesses anticodon that complements a specific codon on mRNA • It has a specific amino acid attachment site for binding a particular amino acid • It has a ribosome recognition site • It consists of about 80 nucleotides, many of which are of unusual nucleotides

  4. Charging of tRNA Fig. 10.32

  5. Composition of ribosome

  6. Initiation of Protein Synthesis • In the absence of mRNA, 30S and 50S subunits remain separated, ensured by the activity of initiation factors 1 and 3 (IF-1 and IF-3) associated with 30S. • If mRNA is present, IF-3 binds to mRNA and thus brings mRNA and 30S together. • The Shine-Dalgarno sequence on mRNA will pair with a region located at the 3’ end of 16S rRNA

  7. Initiation of Protein Synthesis • Next, cytosolic initiator factor 2 (IF-2) complexes with GTP and initiator tRNA (fMet-tRNA) • IF-2 directs binding of fMet-tRNA to P site within 30S subunit, permitting the association of 30S and 50S subunits • IF-3 is then removed from the complex

  8. Initiation Complex Formation Fig. 10.33

  9. Elongation of Protein Synthesis • Elongation factor Tu shuttles proper aa-tRNA into the A site, forming anticodon:codon match • The peptide bond is formed between the incoming aa and the C terminal of the elongated polypeptide, catalyzed by a ribozyme located on 50S subunit • Growing peptide bound to tRNA on A site is moved to the P site with help by Elongation factor G and GTP

  10. Elongation Fig. 10.35

  11. Termination • When translocation brings one of the termination codons into the A site, the ribosome will bind one of the two peptide release factors (RF-1 and RF-2) • The release factor will activate peptidyl transferase, hydrolyzing the bond joining polypeptide to the tRNA at P site. • Ribosome disassembles and recycle to another round of protein synthesis

  12. Termination Fig. 10.35

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