In recombinant DNA technology a substantial number of enzymes are required for modifying DNA for a variety purposes. To modify the DNA one should know what enzymes are required and their properties. It is sine quo non for any student of molecular Biotechnology.
E.coli DNA pol-I:
Its Mol.wt is 109KD. This is extensively used for Nick translation and Random primer mode of labeling. It is also used in the second strand synthesis during cDNA preparation. However it requires a primer or nick for its activity.
DNA Polymerase I; http://www.hindawi.com/
The enzyme from its NH3 end has 5>3 exonucleases 3>5 exonuclease and 5> 3 Polymerase activity. However the recombinant DNA pol-I is available as a truncated form called Klenow fragment (68KD), which has 3>5 exonuclease and 5>>3 Pol activity from its NH3 end. One has to be careful about this enzyme for; the concentration of dNTPs provided should be optimal otherwise instead of polymerase it acts as an exonuclease. If carefully used, one can apply this enzyme, for end filling or blunting dsDNA. Using primers one can produce ds DNA by what is called primer extension method. However this enzyme has medium processivity and fidelity characters.
T7 DNA polymerase:
It mol wt is 84+12 KD (Pol + theoredoxin). This polymerase is synthesized by the viral genome and the host bacterial cell provides the theoredoxin.
Together the enzyme is excellent in its polymerase activity. It has 5>>3 polymerase activity and 3>>5 exonucleases activity. Recombinant methods have produced T7 pol without 3>>5 exonucleases property. This enzyme is called Sequenase for this is an excellent enzyme for sequencing and primer extension protocols and even this can be used for labeling methods. This has high processivity and high fidelity properties.
T4 DNA polymerase:
It is produce by the T4 Phage viral genome. Now it is available as recombinant product. Its Mol.wt is 114KD and consists of single polypeptide chain . This is used for end filling and end labeling protocols. It has 5>>3 pol activity, 3>>5 exonucleases activity. The enzyme is quite stable and it can be substituted for DNA pol-I. If the there are 3 over hangs it remove by 3 exonucleases activity and thus it produces blunt ends. On the contrary if the ds have 3 recessive ends, the enzyme extends the ends by 5 > 3 polymerase activities. However it lacks 5> 3 exonucleases activity.
This enzyme is isolated from thermophilic microbes, such as Thermophilous aquaticus, Pyrococcus species, and Thermococcus litoralis. The enzyme Mol.wt is 85-95KD. They have apparent 5>>3 polymerase activity. And they dont exhibit 3>>5 exonucleases activity. The enzyme is stable for 60 -70m minutes at 92^o temperature. This enzyme is exclusively used for PCR amplification of DNA. However this enzyme has low processivity and low fidelity characters. But recently pFu and ULTMA from Perkin Elmer/ Stratagene have been found to show high fidelity. These enzymes are exclusively and extensively used in PCR based florescent-labeled sequencing reactions.
These enzymes can also be used in Rt-PCR methods. These are also used in pathogen detection protocols. Also used in cDNA library preparations. The amplified ds strands have one A base as extensions. With suitable vectors the CDNA prepared can be directly ligated to dephosphorylated Vector DNAs.
RNA dependent DNA polymerase:
This is also called as Reverse Transcriptase. It Mol.wt ranges from 85KD (from SDS-PAGE it shows 71KD) single polypeptide (murine melony leukemia virus) and 92 KD (two polypeptides called alpha 68KD and Beta 92KD) from Avian Myeloblastasis virus, all of them are retroviruses. These enzymes have RNA dependent DNA polymerase activity, but does not show any apparent 3>>5 exonucleases activity. It can also perform DNA dependent DNA polymerase activity. Another great feature of these enzymes is that they have RNase-H activity, where the enzyme removes by nicking or displacement of RNA when it is hybridized to DNA. It can remove nucleotides from both ends i.e. from 5 and 3 ends. The alpha subunit has contains both Polymerase and RNase -H activity.
A Handy Enzyme
This ribbon representation of the RT active domain illustrates its hand-like structure, showing fingers (blue), palm (pink) and thumb (green). The active site (red atoms), where DNA is elongated, is in the palm region. Also shown is an RT-inhibitor drug (yellow) in the pocket where it binds.
This is extensively used during second strand synthesis of cDNA. It requires RNA or DNA primers of 8 or more nucleotide long. These enzymes show low processivity and low fidelity. In most of the labs this enzyme is used for the preparation of first strand of cDNA. Its high temperature dependence of 42^o is helpful in removing ant secondary structures of the template. But Melony Murine leukemia enzyme is single stranded and it is mostly used in cDNA preparations.
This enzyme is a tetramer 33KD each. It has unique property of adding adenine nucleotides to 3 end of any RNA. Only few nucleotides are required at the 3 end of the RNA.
Some of the viral RNAs dont have poly (A) tail; in such situations one can add poly (A) tail, which is of great help in preparation of ds CDNA from them.
It is tetramer, 60-70KD each. It can add rNDPs to 3 ends of RNA and require Mn2^+ or Mn2^+. This can polymerize free nucleotides to generate polynucleotide chains. It can also act as nuclease.
Polynucleoside Phosphorelase: http://www.creativebiomart.net/
Terminal Deoxynucleotidyl Transferase:
It is a dimmer consists of 26.5 and 8KD proteins. It adds dNTPs to the 3 OH ends ss DNA or dsDNA. It is template independent. This can be used for 3 end labeling. This can also be used for generating 3end tails of required nucleotides for cloning purpose.
T4 Polynucleotide Kinase:
It is obtained from T4 phages. Its molecular mass is 33KD, it is a tetramer. It transfers gamma phosphate from the dATP to the 5 of ds DNA or dsRNA. Even in the presence of 5 P group, it exchanges the gamma labeled phosphate, at the 5 end. This is extensively used for 5end labeling of DNA or RNA probes and the 5 labeled DNA can be used for sequencing reactions.
Structure an mechanism of T4 polynucleotide Kinase; an RNA repair emzymes; http://emboj.embopress.org/
T7 RNA-pol (98KD), T3 RNA-Pol (100KD) and SP6 RNA-pol (96KD) can be used for synthesis of labeled RNA in large amounts provided if one uses their respective promoters in their constructs.
There are different types of ligases of which E.coli DNA-ligase (74-77KD) and T4 DNA ligases (43KD) are extensively used. The former is NAD dependent and the later is ATP dependent. They are responsible for ligating the DNA ends.
Alkaline Phosphotase enzymes are available from bacteria and calf intestine. They are used to remove phosphate groups from 5 ends of ssDNA or from dsDNA.
Alkaline Phosphatase; http://en.wikipedia.org/
Removal phosphate groups in vectors prevent self-ligation. However one should be careful in using this enzyme for after treatment it has be removed completely by extracting the DNA 2 to 3 time in phenol-chloroform and then in chloroform once and precipitating in 95% alcohol in the presence of .15 molar sodium acetate. Alkaline Phosphotase from calf intestine can be easily inactivated by heat.
This enzyme used for capping of mRNA, which is with out it. The enzyme transfers 7CH3-GMP* from the 7CH3-GTP to the 5 biphosphate or triphosphate by 5 to 5 phosphate bonding to generate 57CH3 G-CH2-O-P*-O-P-O-P-O-CH2- ApXpXpX.
Dnase I: RNase free:
The enzyme is available as a recombinant product. Its Mol.wt is 28KD.This enzyme has the ability remove nucleotides from 3 end of ds DNA either from blunt ends or from 3 recessive ends.
3to 5 exonuclease; http://en.wikipedia.org/
It removes nucleotides after nucleotide to generate 5P-mononucleotides. This enzyme is extensively used for deletional analysis of promoters to find out which part of the DNA segment can act as the promoter. If allowed for longer period it can generate single stranded DNA, but this enzyme does not act on single stranded DNA or RNA. This enzyme can also remove Apurinic and Apyrimidinic sites by endonuclease activity.
Lambda 5 Exonuclease:
This ahs the ability remove nucleotides one after another from the 5 end of the ds DNA either from the blunt end or 5 over hangs. This is also useful in generating single stranded DNA and also for deletional analysis of the promoter elements.
It is obtained from Aspergillus oryzae. It removes single stranded DNA or removes over hangs either from 3 or 5 end and produces a blunt ended DNA. Its Mol.wt is 38KD. It is a glycoprotein.
Aspergillus nuclease S (1); http://www.ebi.ac.uk/
Double stranded RNA and RNA: DNA hybrids are resistant to the action of this enzyme. This enzyme can be used S1 mapping of transcripts, one can remove 5 or 3 overhangs of DNA ends, and even they remove any hair pin structures.
The enzyme is obtained in large quantities from retroviral constructs.
RNase H; http://en.wikipedia.org/
The enzyme removes RNA by endonucleolytic cleavage of RNA from RNA: DNA hybrids. This enzyme used in the preparation of the second strand during ds cDNA synthesis.
The main source is bovine pancreas. Its Mol.wt is 13.7 KD. In its pure form it is used for the preparation pure DNA free from RNA contamination in plasmid DNA preparation.
Ribonuclease A; http://en.wikipedia.org/
It hydrolyses 3-5 phophodiester bonds of RNA segments with 23cyclic phosphates.
During preparation of nucleic acid from whole cells containing lot of proteins, to free from proteins this enzyme is used. This gives reasonable nucleic acid preparations
DNA ligase; http://www.biochem.umd.edu/
Bacterial RNA Polymerase; http://smallcollation.blogspot.com/
RNA Pol 1 (III);http://www.conservapedia.com/
RNA Pol II; http://www.conservapedia.com/
Fragment of DNA Pol I-3-5 exonuclease;DNA Pol I also contain 5-3 exonuclease activity http://en.wikipedia.org/