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Team:Paris Liliane Bettencourt/Project/Memo-cell/Microcin
From 2010.igem.org
Memo-Cell project: Microcin
What is microcin C?
Microcins are a class of small (>10-kDa) antibacterial agents produced by Escherichia
coli and its close relatives (1, 2, 15). Microcins are produced from ribosomally synthesized
peptide precursors. The microcin C (McC) is posttranslationally modified by dedicated
maturation enzymes encoded by genes in the microcin C operon mccABCDE (15). McC
is a heptapeptide with covalently attached C-terminal modified AMP (11). The peptide
moiety of McC is encoded by the 21-bp mccA gene, the shortest bacterial gene known
(6). McC (Fig. 1) has a molecular mass of 1,178 Da and contains a formylated N-terminal
methionine, a C-terminal aspartate instead of the asparagine encoded by the mccA gene,
and an AMP residue attached to the
carboxamido group of the modified aspartate
through an N-acyl phosphoramidate bond. The phosphoramidate group is additionally
esterified by a 3-aminopropyl moiety.
How it works?
McC is taken up by E. coli through the action of the Yej- ABEF transporter (11) and is
processed once it is inside the cell. Processing involves deformylation of the N-terminal
Met residue by protein deformylase, followed by degradation by any one of the three
broad-specificity aminopeptidases (peptidases A, B, and N) (9).
Processed McC (Fig. 1) strongly inhibits translation by preventing the synthesis of amino-
acylated tRNAAsp by aspartyl-tRNA synthetase (AspRS) (10).
The tRNA aminoacylation reaction catalyzed by aminoacyl tRNA synthetases includes two
steps. First, the enzyme activates a cognate amino acid by coupling it to ATP and forming
aminoacyl-AMP (aminoacyl-adenylate). The aminoacyl moiety is then transferred to tRNA.
Processed McC is structurally similar to aspartyl-AMP but is not hydrolyzable. Thus,
the inhibition of AspRS results from tight binding of processed McC in place of aspartyl-
adenylate.
Thus, McC is a Trojan horse inhibitor (13): the peptide moiety is required for McC delivery
into sensitive cells, where it is processed with subsequent release of the inhibitory
payload.
Engineering of the microcin C operon.
For our project, we needed to have a inducible death gene, as small as possible (<40bp),
so that it could fit within a recombination site but also could be triggered only when
recombination did not happen, that is to say, when the bacteria did not «count» well.
Hence, microcin C seemed to be the only choice as it is only 24bp long.
However, microcin C is naturally produced by one bacteria to survive in a depleted media
by killing surrounding bacterias, which is the opposite of what we needed.
We had then to engineer to operon so that once induced, the microcin C would kill the
producing bacteria but not the rest of the population.
To do this, we had to tackle three major keypoints:
- 1. Knock-out the gene coding for the membrane transporter responsible for the uptake of
the microcin.
- 2. Knock-out genes within the operon which are responsible for self-immunity against the
microcin
- 3. Mutate the operon so as to delete the four biobrick restriction sites (3 PstI and 1 EcoRI).
