REGULATION OF GENE EXPRESSION
The synthesis and activity of some
enzymes in the cells do not change. These are called structural enzymes.
Some enzymes are affected by environmental conditions.
The cell controls enzymatic reactions mainly in two ways.
1. Regulates enzyme activity
2. Controls enzyme synthesis.
Regulation of Enzyme Activity (posttranslational regulation)
• The enzyme is synthesized as part of a large inactive precursor protein. The enzyme is then separated from this precursor protein.
•The enzyme is degraded and its activity is reduced.
• Feedback inhibition and covalent modification, which reversible and transient regulation of the regulation of enzyme activity, are also used by the cell.
Feedback Inhibition
Inactivation of enzymes with some compounds
In this inhibition, the final product formed in the metabolic pathway inactivates the first enzyme in this pathway.
As a result, the final product is no longer produced.
Allosteric and isoenzymes are used.
Feedback Inhibition
If the amino acid of arginine is over-
synthesized, N-acetyl glutamate synthase (AGS) enzyme is inhibited by arginine,
If proline is excessive, proline inactivates the glutamyl kinase (GK) enzyme.
AGS Arginine
Glutamic acid
GK Proline
Covalent Modification
It is a regulatory mechanism that temporarily inactivates a particular enzyme.
Enzyme activity is controlled by adding or removing some small organic molecules.
Similar to allosteric enzymes, enzyme activity is inhibited by a covalently bonded compound that constitutes a structural change in the enzyme.
Once this compound is removed, the enzyme gains normal activity.
The activity of some enzymes is affected by the addition of AMP, ADP, inorganic phosphate or methyl.
Posttranslational modifications of some proteins are irreversible.
•
mRNA splicing intron•
Protein splicing intein (a peptide)•
This phenomenon is seen in some proteins of archaea, bacteria and eukaryotes.•
DNA gyrase (topoisomerase II)•
Mycobacterium leprae (GyrA protein)Regulation of Enzyme Synthesis
In the control of enzyme synthesis at the level of transcription;
Reduction of synthesis of some enzymes repression,
The increase in the synthesis of some enzymes is called induction
Regulon
E. coli has multiple operons for maltose usage.
These operons are controlled by maltose activator protein.
This type of operon, where more than one operon is controlled by the same regulatory protein, is called regulon.
Regulons are also found in operons with negative control (for example arginine regulone).
1. Two-element regulator systems
It is detected by a sensor and the cell is activated. (signal transduction)
Signal transduction systems consist of two parts (two-element system):
1. Sensor protein in the cell membrane
2. Regulatory protein in the cell
Sensor kinase phosphorylation regulator protein
2. Quorum Sensing
Quorum: Sufficient Number
Sensing: Detection
It is a regulation system
controlled by the cell density of the same species. If there is
sufficient cell number, a specific biological response is generated.
Quorum Sensing
Aliivibrio fischeri bioluminescent property luciferase light lux operons
Autoinductor when acylated homoserine
lactones (AHLs) are in sufficient quantity Lux R active lux operons work light
A long chain aliphatic aldehyde (RCHO) + O2 + Flavin mononucleotide (FMNH2) Luciferase FMN + RCOOH + H2O + light
Lux R activator protein Runs lux operons
Photobacterium spp. Aliivibrio fischeri, Vibrio spp. Facultative,
Pseudomonas aeruginosa, E. coli biofilm
Staphylococcus aureus short peptides
Haloalkalifyl archaea Natronacoccus occutus protease
Eucaryotic Saccharomyces cerevisiae, Candida aromatic alcohols single cell or filaments
Enzyme induction and repression involving DNA binding proteins commonly used by Bacteria and Archaea is the first pathway.
The other way is mostly used by eukaryotes.
Signals are transmitted by protein subunits of the RNA polymerase enzyme.
It is interesting to note that Archaea, whose replication and transcription mechanisms
resemble eukaryotes, are similar to bacteria in terms of transcription regulation.
4. Transcription control of Archaea