DNA ligase enzymes

an enzyme for ligation /joining of two different or same fragments of DNA/RNA

1. by
Dr K. K.Gupta

2. Introduction
•First DNA ligasewas purified and characterized in 1967 by the Gellert,
Lehman, Richardson, and Hurwitz laboratories.
•Although cutting DNA precisely by RE is useful for DNA analysis but its full
potential is only rely when the fragments produced by RE are joined
together to form recombinant DNA..
•This joining is achieved by DNA ligase.
•Ligaseis an enzyme to join any two DNA segment together and process is
called ligation despite of their different origin
For cloning and expression the genomic integrity of vector is
essential,

3. Continued…..
•DNA ligasesplay an essential role in maintaining
genomic integrity by joining breaks in the
phosphodiesterbackbone of DNA that occur during
•replication and recombination, and
•Repair of damaged DNA.
•In Biotechnology used to Integrate the DNA fragments
in to the vector
•

5. Source of ligase.
•Though ligaseis of universal occurrence in
living organism and viruses but for use in RDT
it is isolated from two sources
•E.coli. 75 Kda.
•T4 bacteriophage68 KDa-first ATP-
dependent ligaseenzyme to be discovered
and is widely used in molecular biology,
•The enzyme isolated from bacteria E.coliis a
polypeptide chain with mol.wtof

6. Types of ligase
•E.coliDNA ligase-Monomeric, MW=74 kDa
•T4 Ligase
•Ampligase
•Genetically engineered ligase
•The RNA ligasefor RNA fragments ligation .catalyzes
the formation of 3′ → 5′phophodiesterbondsetween
3′-OH and 5′-P groups of RNA molecules.
•Repairing of Anticodonloop
•

7. Substrate of ligase
varioussubstratessuch as DNA nicks, DNA
fragments with various lengths cohesive ends,
DNA fragments with blunt ends and some
DNA/RNA hybrids.

8. Ligase in Biotech
DNA Ligase
•+ In all except Viruses but only
E coli DNA ligaseis used in
biotech .
•Use NAD as cofactor
•Can not ligateblunt end DNA
fragments
•cannot join RNA to DNA
efficiently
•Narrowness activity (specifity
for chohesiveends joining
T4 Ligase
•Bacteriophageand most
commonly used
•ATP as cofactor
•ligateeither cohesive or blunt
ends of DNA fragments , as
well as RNA and RNA-DNA
hybrids, but not single-
stranded nucleic acids
•Ligateblunt ended DNA with
much greater efficiency than E
coli DNA ligase
•Can not join ssDNA
•Also join ssnick in dsDNA and
RNA-DNA Hybrud
•Broad activity

9. Genetically engineered T4 Ligase
•Some engineering has been done to improve
thein vitroactivity of T4 DNA ligase; one
successful approach, for example, tested T4
DNA ligase fused to several alternative DNA
binding proteins and found that the constructs
with either p50 orNF-KBas fusion partners
were over 160% more active in blunt-end
ligations for cloning purposes than wild type
T4 DNA ligase

10. Ligation efficiency
Depends upon types of end sticky/ blunt
Sticky –efficient
Blunt –less efficient and need more concentration of ligase

11. Activity and Mechanism of ligaseaction
•If two different DNA are treated with same restriction enzyme to give fragments
with complementary cohesive ends /sticky ends and mixed then two DNA will join
by forming phosphester bond between terminal nucleotides (5’phophoryl at the
end of one strand i.e donor )and 3’OH at other end i.e acceptor but it has nick
after
ATP is required which proceed in three steps
•1.adenylation–addition of AMP in the active centre of ENz. And PP is released
2.,transfer of the AMP to the 5”P so called donor and formation of pyrophosphate
bond
•3. Formation of phosphodiester bonds )
•T4 ligase catalyzes end to end joining.
•This could occur inter/intra molecular but inter molecular joining is correct.
•Ligation requires ATP and is carried at 4 deg celcius to lower the kinetic energy.
•This reduce the separation of paired sticky end which is later stabilized by ligation.
However, long reaction times are needed to compensate the low activity of DNA
ligase in cold.

12. Mechanisms

13. Weiss unit-
The amount of ligasethat catalyzes the
exchange of 1 nmoleof
32
P from
inorganicpyrophosphate to ATP in 20
minutes at 37
°
C.
This is the one most commonly used.

14. enhancer for DNA ligase
•The activity of E. coli DNA ligasecan be enhanced
byDNA POLat the right concentrations.
Enhancement only works when the
concentrations of the DNA polymerase 1 are
much lower than the DNA fragments to be
ligated. When the concentrations of PolI DNA
polymerases are higher, it has an adverse effect
on E. coli DNA ligase
•The T4 enzyme concis kept high and PEGis
added to reaction mixture for stimulation.

15. Blunt end ligation
•`
•Blundend fragment has no overhang which can
hold the two fragment temporarily together.
•So ligaseand DNA concentration are kept high .
•It is therefore used to ligatethe two DNA
fragments obtained by two different restriction
enzyme with non compatible sticky ends DNA.
The non complementary DNA are removed prior
to ligation using enzyme SI nuclease which digest
SS DNA

16. For this
•Blunt ended fragments are linked with the linker and adapter
before joining
•Linkers & Adaptors
•Recombinant DNA and gene cloning use RE to cut DNA at specific
site .
•If suitable sites are not available for manipulation then these
cleavage sites can be added as linker or adaptor
•Linkers are synthetic SS DNA of 8-14 bases with Res. Sites for 3-8
RE which will self reassociateto form DS DNA
•For eg5’ CCGAATTCGG 3’ CCGAATTCGG
• GGCTTAAGCC
•It contains ECOR I site . This sequence can be ligatedto blunt end
and then digested with Rest enz. Cohesive end is produced.

18. Application
•DNA ligase is important enzymatic tools without which RDT can not be achieved.
•The important function are:-
•Involves in ligation or joining of two DNA segments.
•Like –
•Two okazaki fragments in replication The fragments are formed of lagging strand and after removal of
primer the DNA segments are joined together two give continuous strand of DNA against 5’-3’ template
strand.
•It is used in Ligation of DNA in Vector for cloning & expression.
•Used in Ligation of linker and adaptor at the blunt ends of DNA fragments
•Used in Sealing of nick in DNA fragments
•2.It I also used in ELISA to form Enzyme substare conjugate . P-nitrophenyl phosphate is a substrate
for AP but cannot form conjugate to give coloured product . The Ap remove P and forms a conjugate
•Note .
•Self ligation is prevented by use of Alkaline phosphatase. De phophorylated Vector DNA cannot be
recircularised in the cloning procedure and can be remain linear for ligating with the other DNA.
•Ligase requires 3’OH and 5’PO4 for ligation

19. DNA LIGASE …….