Blog. 18 December Prezi Awards The best presentations have arrived. 5 December Do this, not that: Keynote speech. 28 November Wady i Zalety Klonowania Idea 1. Idea 2. Rozmnażanie bezpłciowe – naturalne klonowanie. Klonowanie zachodzi przez: Klonowanie DNA. KLONOWANIE Klony DNA służą do: Co to jest klonowanie? Klonowanie – tworzenie genetycznej kopii fragmentu DNA, komórki lub organizmu.

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Recombinant proteins like these are often made in bacteria.

In some genetic disorders, patients lack the functional form of a particular gene. Now the next question, and I’m over simplifying things fairly dramatically is well you now have a bunch of bacteria that have a bunch of copies of that gene, how do you make klonoanie of it?

Campbell biology edycja 10, strony And this is amazing because obviously DNA, this isn’t stuff that we can, you know, manipulate with our hands the way that we would copy and paste things with tape.

Selekcja i transformacja u bakterii.

And a plasmid is a piece of genetic material that sits outside of chromosomes but it can reproduce along, or I guess we can say can replicate along with the machinery of the, the genetic machinery klonnowanie the organism.

The purified protein can be used for experiments or, in the case of insulin, administered to patients.

Selekcja i transformacja u bakterii (artykuł) | Khan Academy

It’s going to take in the plasmid. DNA cloning is a very common technique that is used in a huge variety of molecular biology applications. As an example, let’s see how DNA cloning can be used to synthesize a protein such as human insulin in bacteria.

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Then, we give the bacteria a chemical signal that instructs them to make the target protein. Thus, bacteria that took up the plasmid can be selected on nutrient plates containing the antibiotic.

File:Gene cloning PL.svg

You put these plasmids in the presence of the bacteria or you provide some type of a shock, maybe a heat shock, so that some kponowanie the bacteria takes it up and then the bacteria starts reproducing. For instance, when we try to klonowaanie a gene into a plasmid using a particular restriction enzyme, we may get some cases where the plasmid closes back up without taking in the geneand other cases where the gene goes in backwards.

And usually it’s a piece of DNA that codes for something we care about, it is a gene that will express itself as a protein that we think is useful in some way. This is the bacteria. And so just like that you can take this, you can take this colony right over here, and put it into another solution or continue to grow it and you will have multiple copies of that gene that are inside of that bacteria. So let me draw, so here we have a plate to grow our bacteria on, and it has nutrients right over here that bacteria can grow on.

Methods like restriction enzyme digestion and PCR are commonly used to check the plasmids. Protein production and purification. Diagram klonowajie a plasmid. Well, the first thing we dn do is we wanna cut this gene out some how. Each surviving bacterium will give rise to a small, dot-like group, or colonyof identical bacteria that all carry the same plasmid.

Thus, the protein of interest is trapped in the column, while the other molecules are washed away. If you’re cloning an animal or an organism, like a sheep, well then you are creating an animal that has dnaa exact genetic material as the fna animal. Which is all about making identical copies of a piece of DNA. The bacteria that make colonies should all contain a plasmid which provides antibiotic resistance.


Selekcja i transformacja u bakterii

Use antibiotic selection to identify the bacteria that took up the plasmid. A recombinant plasmid where the target gene is inserted after the promoter, pointing in the forward direction oriented so that it’s transcribed to make an mRNA that specified the desired protein.

And plasmids tend to be circular DNA so we will paste it into a plasmid. Transformation and selection of bacteria are key steps in DNA cloning.

Jlonowanie i transformacja u bakterii. You’re making these solutions and you’re applying the restriction enzymes.

Harvest the protein from the bacteria and purify it. I don’t want to have to take the trouble of keep drawing the multiple strands. Insulin capture from human ,lonowanie. DNA ligase, to connect the backbones right over here. These, those things right over there those are restriction enzymes. So how do we do that? And the technique that’s typically done is giving some type konowanie a shock to the system that makes the bacteria take up the plasmids.

The basic steps are:. In CK biology advanced concepts. You could just let them grow but there’s a problem here.