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2 component regulatory systems Maltose=effector, BUT if signal not DIRECTLY involved, but needs to be transmitted and changed = signal transduction Sensor.

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Presentation on theme: "2 component regulatory systems Maltose=effector, BUT if signal not DIRECTLY involved, but needs to be transmitted and changed = signal transduction Sensor."— Presentation transcript:

1 2 component regulatory systems Maltose=effector, BUT if signal not DIRECTLY involved, but needs to be transmitted and changed = signal transduction Sensor protein= –kinase, phosphorylates compounds, –membrane associated Phosphoryl group transmitted to another regulator IN the cell –Often a DNA binding protein involved in transcription Many examples, N-fixation, sporulation,chemotaxis

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3 Chemotaxis Attractants decrease rate of autophosphorylation Repellant increased autophosphorylation CheA-CheW=transducer CheY controls switch –cheY-P tumbles, CCW-CW CheB phosporylated by CheA-P, but slower response than CheY-P CheB involved methylation –Fully methylated = best for repellants –cheB-P demethylates, occurs when attractants High –Degree of methylation regulates attraction/repulsion

4 Chemotaxis

5 Genetic exchange: transformation

6 Genetic exchange: plasmid transfer Small, usually circular, independently replicating DNA molecules –Generally, G - plasmids replicate as does chromosomal DNA, G + plasmids by “rolling circle” replication Genes of replication control, timing initiation on plasmid (ori) –Some plasmids integrate (F +, Hfr) –Most are double-stranded –About 1- 100kb Code for: –R-factors (R-plasmids) : antibiotic resistance, heavy metal resistance –Virulence plasmids : adhesins, hemolytic factors, toxin, Ti, bacteriocins –Degradation, tol, nah, Plasmid copy # Compatibility (inc)

7 Genetic exchange: plasmid transfer Small, usually circular, independently replicating DNA molecules –Generally, G - plasmids replicate as does chromosomal DNA, G + plasmids by “rolling circle” replication Genes of replication control, timing initiation on plasmid (ori) –Some plasmids integrate (F +, Hfr) –Most are double-stranded –About 1- 100kb Code for: –R-factors (R-plasmids) : antibiotic resistance, heavy metal resistance –Virulence plasmids : adhesins, hemolytic factors, toxin, Ti, bacteriocins –Degradation, tol, nah, Plasmid copy # Compatibility (inc)

8 Avery Experiment

9 Transformation Competence: ability to be transformed Steps in transformation –DNA binding and uptake (SS or DS, depending on species) –Integration (recA) Competence may be induced by electroporation, Ca

10 Mechanism of transformation

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12 Transduction Generalized— low frequency Specialized— high frequency:requires specific integration

13 Generalized transduction

14 Specialized transduction

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16 Genetic exchange: conjugation

17 Conjugation: early Cell-surface structure

18 Conjugation: middle

19 Conjugation: late

20 Genetic Engineering-basics Basic steps in cloning –Restriction-modification enzymes –“shot gun” or PCR –Ligase –Recombination Plasmids (or phage)= vectors –Expression vectors Selection of clones Looking for a clone with a specific gene –Probes (DNA, RNA or antibody) Wave of the future: DNA chips or “microarrays”, BAC libraries, automated sequencing etc

21 Genomics Bioinformatics Harvesting genes for biotech (Diversa) –Recent Science article Comparing gene families


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