The Basics of Recombinant DNA

rDNA stands for recombinant DNA. Before
we get to the "r" part, we need to understand DNA. Those of you with
a background in biology probably know about DNA, but a lot of ChemE's haven't
seen DNA since high school biology. DNA is the keeper of the all th

Recombinant DNA is the general name for taking a piece of one DNA, and

and combining it with another strand of DNA. Thus, the name recombinant!

Recombinant DNA is also sometimes referred to as "chimera." By combining two or

more different strands of DNA, scientists are able to create a new strand of DNA.

The most common recombinant process involves combining the DNA of two

different organisms.

How is Recombinant DNA made?

There are three different methods by which Recombinant DNA is made. They are

Transformation, Phage Introduction, and Non-Bacterial Transformation. Each are described separately below.

Transformation

The first step in transformation is to select a piece of DNA to be inserted

into a vector. The second step is to cut that piece of DNA with a restriction

enzyme and then ligate the DNA insert into the vector with DNA Ligase. The insert contains a selectable

marker which allows for identification of recombinant molecules. An antibiotic marker is often used so a host cell without a vector dies when exposed to a certain antibiotic, and the host with the vector will live because it is resistant.

The vector is inserted into a host cell, in a process called transformation. One example of a possible host cell is E. Coli. The host cells must be specially prepared to take up the foreign DNA.

Selectable markers can be for antibiotic resistance, color changes, or any other characteristic which can distinguish transformed hosts from untransformed hosts.

Different vectors have different properties to make them suitable to different applications. Some properties can include symmetrical cloning sites, size, and high copy number.

Non-Bacterial Transformation

This is a process very similar to Transformation, which was described above. The only difference between the two is non-bacterial does not use bacteria such as E. Coli

for the host. In microinjection, the DNA is injected directly into the nucleus of the cell being transformed. In biolistics, the host cells are bombarded with high velocity microprojectiles, such as particles of gold or tungsten that have been coated with DNA.

 

Phage Introduction

Phage introduction is the process of transfection, which is equivalent to transformation, except a phage is used instead of bacteria. In vitro packagings of a vector is used.

This uses lambda or MI3 phages to produce phage plaques which contain recombinants. The recombinants that are created can be identified by differences in the recombinants and non-recombinants using various selection methods.

How does rDNA work?

Recombinant DNA works when the host cell expresses protein from the recombinant genes. 

A significant amount of recombinant protein will not be produced by the host unless expression

factors are added. Protein expression depends upon the gene being surrounded by

a collection of signals which provide instructions for the transcription and translation

of the gene by the cell. These signals include the promoter, the ribosome binding

site, and the terminator. Expression vectors, in which the foreign DNA is inserted, contain these signals. Signals are species specific.  In the case of E. Coli, these signals must be E. Coli signals as E. Coli is unlikely to understand the signals of human promoters and terminators. Problems are encountered if the gene contains introns or contains signals which act as terminators to a bacterial host. This results in premature termination, and the recombinant protein may not be processed correctly, be folded correctly, or may even be degraded. Production of recombinant proteins in eukaryotic systems generally takes place in yeast and filamentous fungi. The use of animal cells is difficult due to the fact that many need a solid support surface, unlike bacteria, and have complex growth needs. However, some proteins are too complex to be produced in bacterium, so eukaryotic cells must be used.

Why is rDNA important?

Recombinant DNA has been gaining in importance over the last few years, and recombinant DNA will only become more important in the 21st century as genetic diseases become more prevelant and agricultural area is reduced.  Below  are some of the areas where Recombinant DNA will have an impact.

Better Crops (drought heat resistance)

Recombinant Vaccines (ie. Hepatitis B)

Prevention and cure of sickle cell anemia

Prevention and cure of cystic fibrosis

Production of clotting factors

Production of insulinProduction of recombinant pharmaceuticals

Plants that produce their own insecticides

Germ line and somatic gene therapy

What does the future hold?

Now that we've figured out the basics behind what Recombinant DNA are, it's time to look at how Recombinant DNA will impact the future. 

 

 


Sohan hossain

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