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Published bykosa zoli Modified over 6 years ago
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E. coli RNA polymerase (redux) Functions of other subunits: α - binds the UP element upstream of very strong promoters (rRNA), and some protein activators. β - active site of Pol, also binds , nascent RNA, RNA-DNA hybrid, and DS DNA in front of bubble. β' - also binds , nascent RNA, RNA-DNA hybrid, and DS DNA in front of bubble.
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From Fig 6.35 Thermus aquaticus RNAP core. “The Claw”
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T. Aquaticus Holoenzyme Similar to Fig. 6.37
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RNAP binds/protects DNA from bp -44 to +3
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Fig. 6.40 DNA used to form the RF Complex Locks the enzyme into the open promoter complex.
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Fig. 6.41a, RF Complex
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Figure 6.41b, RF with removed
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Fig 6.43b RF Model with removed.
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RNAP: Backsliding and Editing 1.If wrong nucleotide incorporated, elongation can become arrested. 2.Backsliding now competes with elongation: –Pol backs up, extruding some of nascent RNA 3.Gre proteins activate RNAP core to cleave small piece that has wrong nucleotide. 4.Pol starts elongating again.
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Square is the next NTP to be added. Green – nascent RNA that will be cleaved off Red – “older RNA” RNAP core
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Gene Regulation in Prokaryotes Regulation occurs at every level: 1.Gene organization (operon co-expression) 2.Transcription (repression, activation, attenuation) 3.mRNA stability (affected by translation and the 3’ stem-loops), have “degradosome” 4.Translation (repression, activation and autoregulation) 5.Protein stability and other modifications TRANSCRIPTIONAL CONTROL DOMINANT!
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Lactose (Lac) Operon Diauxic growth (2 phases or types, which use different substrates) Operon organization Negative and positive regulation –Lac Repressor (lacI gene) –Catabolite Activator Protein (crp gene)
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Diauxic growth of E. coli on a mixture of lactose + glucose. If E. coli presented with glucose & lactose, use mainly glucose until gone, then use lactose.
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O OH CH2OH O OH CH2OH O HO OH galactose glucose lactose Lactose Structure & Metabolism
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Figure 7.3 Lac Operon: Repression
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Inducer : Allolactose, produced by lacZ - 1,6 linked Fig. 7.4 A side reaction of lacZ.
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J. Monod F. Jacob A. Lwoff 1965 Nobel Prize in Physiology or Medicine (for their work on the lac operon and bacterial genetics)
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Example: lacI + DNAo ↔ lacI-DNAo lacI – lac repressor DNAo – lac operator DNA K d = [lacI] [DNAo] ∕ [lacI-DNAo] K d = equilibrium dissociation constant 1 x 10 -8 to 10 -12 M = high affinity Equilibrium DNA – Protein Binding
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Figure 7.6 Lac repressor binding to lac operator. IPTG = synthetic inducer of lac operon.
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Figure 7.7
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There are really 3 operator regions for the Lac Operon. CAP – activator protein RNAP – RNA polymerase Fig 7.10
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DNAs introduced into E. coli genome of a lacZ mutant using λ phage. LacI gene was present in the chromosome. IPTG was used to induce lacZ. Numbers are based on the ratio of lacZ activity in the presence and absence of inducer (IPTG). Operators work cooperatively (synergistically).
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Structural basis for cooperativity of operators: Lac repressor can bind 2 operator sequences. LacI Tetramer (2 dimers held together at the bottom) DNA Fig 7.12a
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