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NCERT Exemplar · Q38

Q.What would happen when one grows a recombinant bacterium in a bioreactor but forget to add antibiotic to the medium in which the recombinant is growing?

Telangana TsbieShort· 2mImportance★★★★★
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Without antibiotic selection pressure, non-recombinant bacteria will outgrow the recombinant ones, eventually dominating the culture and drastically reducing or eliminating the yield of the desired recombinant protein.

The bioreactor is where the magic of industrial-scale biotechnology happens. You've successfully inserted your gene of interest into a plasmid, transformed bacteria with it, and now you're scaling up from a petri dish to hundreds of litres of nutrient-rich medium. But there's a catch that every molecular biologist learns the hard way: recombinant bacteria carry a burden that their wild-type cousins don't.

When you engineer a bacterium to carry a recombinant plasmid, you're asking it to do extra work. The plasmid itself must be replicated every time the cell divides, consuming energy and cellular resources. More importantly, if that plasmid carries a gene for a foreign protein—say, human insulin or a therapeutic enzyme—the bacterium must transcribe and translate that gene, diverting even more resources away from its own growth and reproduction. This is metabolic burden, and it puts recombinant bacteria at a competitive disadvantage.

Now picture what happens in your bioreactor when you forget the antibiotic. The recombinant plasmid you've inserted almost always carries an antibiotic resistance gene—ampicillin resistance, tetracycline resistance, or another marker. This isn't just a label; it's your selection tool. In the presence of the antibiotic, only bacteria carrying the plasmid can survive. But remove that antibiotic, and suddenly the playing field changes.

A small number of bacteria will inevitably lose their plasmids during replication. This happens spontaneously at low frequency—a daughter cell might not receive a copy of the plasmid, or the plasmid might be degraded. In a normal scenario with antibiotic present, these plasmid-free cells die immediately. But without antibiotic selection, they survive. And here's the problem: these non-recombinant bacteria, unburdened by the metabolic cost of maintaining and expressing foreign DNA, grow faster. They divide more quickly, and with each generation, their proportion in the culture increases.

Important

Bacteria without the plasmid have a growth advantage because they don't waste resources on plasmid replication or foreign protein synthesis. In the absence of selection pressure, they will outcompete recombinant cells. …

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