How can bacteria synthesize human insulin?

In summary, eukaryotic genes have features that are incompatible with prokaryotes. To express a eukaryotic gene in bacteria, the coding sequence must be isolated and inserted into a plasmid with bacterial regulatory sequences. Despite sharing the same genetic code, sometimes tRNA differences may require codon optimization. However, some human proteins may require posttranslational modifications that cannot be performed in bacteria, necessitating the use of eukaryotic expression systems.
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haael
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I have just read that genetically modified e. coli can synthesize human insulin.

But I wonder.

Human (eucaryotic) genes have all kinds of introns, regulators, starting sequences etc. Bacteria don't have all of those. How can a procaryota produce an eucaryotic peptide? Has the insulin gene been "flattened" before inserted into e. coli?
 
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Yes, you are correct that eukaryotic genes have many features that are incompatible with prokaryotes. In order to express a eukaryotic gene in bacteria, you must take only the coding sequence, removing any introns, and regulatory sequences in the untranslated regions, then insert the coding sequence into a plasmid that contains the appropriate regulatory sequences for bacteria. Because eukaryotes and prokaryotes share the same genetic code, bacteria are able to produce the correct amino acid sequence from a eukaryotic DNA sequence (however, tRNA abundances differ between species, so sometimes it is helpful to optimize the codons in the coding sequence by replacing codons for rare E. coli tRNAs with codons for more common E. coli tRNAs).

Of course, this procedure does not always work. Some human proteins (for example, erythropoietin) require specific posttranslational modifications (like glycosylation) that cannot be performed in bacteria. In these cases, eukaryotic expression systems are required.
 
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1. How can bacteria produce human insulin?

Bacteria can produce human insulin through a process called recombinant DNA technology. This involves inserting the gene for human insulin into the bacterial DNA, allowing the bacteria to produce insulin that is identical to the one produced by humans.

2. What type of bacteria is used to synthesize human insulin?

The most commonly used bacteria for synthesizing human insulin is Escherichia coli, also known as E. coli. This bacteria is easy to grow, has a fast replication rate, and is well-studied, making it a suitable organism for producing large quantities of insulin.

3. How is the insulin gene inserted into the bacterial DNA?

The insulin gene is inserted into the bacterial DNA using a plasmid, which is a small circular piece of DNA that can be easily manipulated in the laboratory. The plasmid is cut using restriction enzymes, and the insulin gene is inserted into the cut site. The plasmid is then introduced into the bacteria, where it is incorporated into the bacterial DNA.

4. What are the benefits of using bacteria to synthesize human insulin?

There are several benefits to using bacteria for synthesizing human insulin. Firstly, bacteria are easy and inexpensive to grow, making the production of insulin more cost-effective. Secondly, bacteria can produce large quantities of insulin, meeting the high demand for this hormone. Lastly, the insulin produced by bacteria is identical to human insulin, making it safe and effective for use in patients.

5. Are there any risks or drawbacks to using bacteria for insulin synthesis?

While bacteria have been used successfully to produce insulin, there are some potential risks and drawbacks. One concern is the possibility of contamination, which could lead to the production of impure insulin. Additionally, there is a risk of the bacteria mutating and producing insulin with altered properties. However, strict quality control measures are in place to minimize these risks and ensure the safety and effectiveness of the produced insulin.

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