The document summarizes a seminar on the Ti plasmid. It discusses that the Ti plasmid is found in Agrobacterium tumefaciens and is responsible for crown gall tumor formation in plants. It describes the organization and structure of the Ti plasmid, including the T-DNA region flanked by borders that is transferred to plant cells. Two common vector systems used for plant transformation, the cointegrate vector and binary vector, are explained. The cointegrate vector involves integration of an intermediate vector with the Ti plasmid, while the binary vector separates the plasmid and virulence genes. Finally, the general process of Agrobacterium-mediated plant transformation is outlined.
An overview of the Agrobacterium-mediated gene transfer process. Moreover, studied different kinds of Agrobacterium species are involved in this mechanism.
Agrobacterium is a rod-shaped, Gram-negative bacteria found mostly in the soil. It is a plant pathogen that is responsible for causing crown gall disease in them. This bacteria is also known as the natural genetic engineer because of it's the ability to integrate its plasmid Gene into the plant genome.
Agrobacterium tumefaciens transfer of their genetic material T-DNA of Ti-plasmid into the plant cell: A: Agrobacterium tumefaciens; B: Agrobacterium genome; C: Ti Plasmid : a: T-DNA , b: Vir genes , c: Replication origin , d: Opines catabolism genes; D: Plant cell
A Ti-Plasmid (tumor-inducing plasmid) is a ds, circular DNA that often, but not always. It's a piece of genetic equipment that transfers genetic material from bacterial cells means Agrobacterium tumefaciens into plant cells used to induce tumors in the plant. The Ti-plasmid is damage when Agrobacterium is grown above 28 °C. Such cured bacteria don't induce crown gall disease in the plant due to they are avirulent. The Ti-Plasmid are classified into two types on the basis of opine genes are present in T-DNA.
The Plasmid has 196 genes that code for 195 proteins. There is no one structural RNA. The plasmid is 206.479 nucleotides long. the GC content is 56% and 81% of the genetic material is coding genes.
The modification of this plasmid is a very important source in the production of transgenic plants.
The T-DNA must be cut out of the circular plasmid. A VirD1/D2 complex nicks the DNA at the left and right border sequences. The VirD2 protein is covalently attached to the 5' end. VirD2 contains a motif that leads to the nucleoprotein complex being targeted to the type IV secretion system (T4SS).
In the cytoplasm of the recipient cell, the T-DNA complex becomes coated with VirE2 proteins, which are exported through the T4SS independently from the T-DNA complex. Nuclear localization signals, or NLS, located on the VirE2 and VirD2 are recognized by the importin alpha protein, which then associates with importin beta and the nuclear pore complex to transfer the T-DNA into the nucleus. So that the T-DNA can integrate into the host genome.
We inoculate Agrobacterium containing our genes of interest, onto wounded plant tissue explants. The Agrobacterium then transfers the gene of interest into the DNA of the plant tissue.
An overview of the Agrobacterium-mediated gene transfer process. Moreover, studied different kinds of Agrobacterium species are involved in this mechanism.
Agrobacterium is a rod-shaped, Gram-negative bacteria found mostly in the soil. It is a plant pathogen that is responsible for causing crown gall disease in them. This bacteria is also known as the natural genetic engineer because of it's the ability to integrate its plasmid Gene into the plant genome.
Agrobacterium tumefaciens transfer of their genetic material T-DNA of Ti-plasmid into the plant cell: A: Agrobacterium tumefaciens; B: Agrobacterium genome; C: Ti Plasmid : a: T-DNA , b: Vir genes , c: Replication origin , d: Opines catabolism genes; D: Plant cell
A Ti-Plasmid (tumor-inducing plasmid) is a ds, circular DNA that often, but not always. It's a piece of genetic equipment that transfers genetic material from bacterial cells means Agrobacterium tumefaciens into plant cells used to induce tumors in the plant. The Ti-plasmid is damage when Agrobacterium is grown above 28 °C. Such cured bacteria don't induce crown gall disease in the plant due to they are avirulent. The Ti-Plasmid are classified into two types on the basis of opine genes are present in T-DNA.
The Plasmid has 196 genes that code for 195 proteins. There is no one structural RNA. The plasmid is 206.479 nucleotides long. the GC content is 56% and 81% of the genetic material is coding genes.
The modification of this plasmid is a very important source in the production of transgenic plants.
The T-DNA must be cut out of the circular plasmid. A VirD1/D2 complex nicks the DNA at the left and right border sequences. The VirD2 protein is covalently attached to the 5' end. VirD2 contains a motif that leads to the nucleoprotein complex being targeted to the type IV secretion system (T4SS).
In the cytoplasm of the recipient cell, the T-DNA complex becomes coated with VirE2 proteins, which are exported through the T4SS independently from the T-DNA complex. Nuclear localization signals, or NLS, located on the VirE2 and VirD2 are recognized by the importin alpha protein, which then associates with importin beta and the nuclear pore complex to transfer the T-DNA into the nucleus. So that the T-DNA can integrate into the host genome.
We inoculate Agrobacterium containing our genes of interest, onto wounded plant tissue explants. The Agrobacterium then transfers the gene of interest into the DNA of the plant tissue.
Introduction
Ti plasmid
Agrobacterium tumefaciens
Ti plasmid structure
Overview of infection process
Ti plasmid derived vector systems
Cointegrate vectors
Binary vectors
Agrobacterium mediated transformation of explants
Conclusions
References
MBB 501 PLANT BIOTECHNOLOGY
INFORMATION ABOUT DIFFERENT DNA MODIFYING ENZYMES
WHAT IS AN ENZYME?
Alkaline Phosphatase
Polynucleotide kinase
Terminal deoxyneucleotidyl transferase
Nucleases
Exonuclease
Bal31 Exonuclease III
Endonuclease
S1 endonulease
Deoxyribonuclease 1 (Dnase 1)
RNase A
RNase H
Restriction Endonuclease
PvuI
PvuII
Different types of endonuclease enzymes
The recognition sequences for some of the most frequently used restriction endonucleases.
Categorization of enzymes
Isoschizomers
Neoschizomers
Isocaudomers
BAC & YAC are artificially prepared chromosomes to clone DNA sequences.yeast artificial chromosome is capable of carrying upto 1000 kbp of inserted DNA sequence
Presented by- MD JAKIR HOSSAIN
Doctoral Research Scholar
Department of Agricultural Genetic Engineering ,
Faculty of Agricultural Sciences and Technologies,
Nigde Omer Halisdemir University, Turkey
E. Mail- mjakirbotru@gmail.com
This presentation covers a general introduction to expression vector, its components, types, and its application. Then it covers some of the expression system with examples.
Introduction
Ti plasmid
Agrobacterium tumefaciens
Ti plasmid structure
Overview of infection process
Ti plasmid derived vector systems
Cointegrate vectors
Binary vectors
Agrobacterium mediated transformation of explants
Conclusions
References
MBB 501 PLANT BIOTECHNOLOGY
INFORMATION ABOUT DIFFERENT DNA MODIFYING ENZYMES
WHAT IS AN ENZYME?
Alkaline Phosphatase
Polynucleotide kinase
Terminal deoxyneucleotidyl transferase
Nucleases
Exonuclease
Bal31 Exonuclease III
Endonuclease
S1 endonulease
Deoxyribonuclease 1 (Dnase 1)
RNase A
RNase H
Restriction Endonuclease
PvuI
PvuII
Different types of endonuclease enzymes
The recognition sequences for some of the most frequently used restriction endonucleases.
Categorization of enzymes
Isoschizomers
Neoschizomers
Isocaudomers
BAC & YAC are artificially prepared chromosomes to clone DNA sequences.yeast artificial chromosome is capable of carrying upto 1000 kbp of inserted DNA sequence
Presented by- MD JAKIR HOSSAIN
Doctoral Research Scholar
Department of Agricultural Genetic Engineering ,
Faculty of Agricultural Sciences and Technologies,
Nigde Omer Halisdemir University, Turkey
E. Mail- mjakirbotru@gmail.com
This presentation covers a general introduction to expression vector, its components, types, and its application. Then it covers some of the expression system with examples.
What are an expression vector? Detailed description of plant gene structure. Plant expression vector systems are generally consists of Ri and Ti plasmids.
The other vectors which are generally used are DNA and RNA viruses.
Agrobacterium mediated gene transfer, Ti-plasmid, cloning vectors based on Ti-plasmid, advantages disadvantages regarding cloning vectors based on Ti-plasmid are major areas covered in this Presentation.
This bacterium has a large plasmid that induces tumor, and for this reason, it was named tumor-inducing (Ti) plasmid.
This is process of altering the genetic makeup of an organism using Recombinant DNA Technology.
description of Ti plasmid derivatives as vector and explanation of T DNA and cointegrate vectors and binary vectors and its uses and advantages and disadvantages
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Ethnobotany in herbal drug evaluation,
Impact of Ethnobotany in traditional medicine,
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The people of Punjab felt alienated from main stream due to denial of their just demands during a long democratic struggle since independence. As it happen all over the word, it led to militant struggle with great loss of lives of military, police and civilian personnel. Killing of Indira Gandhi and massacre of innocent Sikhs in Delhi and other India cities was also associated with this movement.
2. INTRODUCTION
DEFINITION
ORGANIZATION OF Ti PLASMID
STRUCTURE OF Ti-PLASMID
T-DNA TRANSFER & INTEGRATION
Ti PLASMID-DERIVED VECTOR SYSTEMS
COINTEGRATE VECTOR
ADVANTAGES OF COINTEGRATE VECTOR
USES OF COINTEGRATE VECTORS
BINARY VECTOR
ADVANTAGES OF BINARY VECTOR
USES OF BINARY VECTORS
PLANT TRANSFORMATION TECHNIQUE USING AGROBACTERIUM
CONCLUSION
REFERENCE
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Ti PLASMID
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3. Almost 100 years ago (1907), Smith & Townsend postulated that a
bacterium was the causative agent of Crown gall tumors.
A tumefaciens infects wounded or damaged plant tissues, it induces the formation of a
plant tumor called crown gall.
The entry of the bacterium into the plant tissues is facilated by the release of certain
phenolic compounds (acetosyringone,hydroxyacetosyringone) by the wounded sites.
Crown gall formation occurs when the bacterium release its Ti plasmid into the plant cell
cytoplasm.
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4.
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A fragment of Ti plasmid, referred to as T-DNA, is actually transferred from the bacterium
into the host where it gets integrated into the plant cell chromosome.
Thus, crown gall disease is a naturally evolved genetic engineering process.
Crown gall formation is the consequence of the transfer integration and expression of genes
of T-DNA of A.tumefaciens in the infected plant.
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5. Ti plasmid-: The large-sized tumor inducing plasmid found in Agrobacterium
tumefaciens. It directs crown gall formation in certain plant species.
&
As A.tumefaciens infects wounded or damaged plant tissues, in induces the
formation of a plant tumor called crown gall or Ti-plasmid.
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6. The Ti plasmid (approx.size 200 kb each) exist as independent replicating circular
DNA molecules within the Agrobacterium cells.
The T-DNA is variable in length in the range of 12 to 24 kb.
The Ti plasmid has three important region:-
1. T-DNA region: This region has the genes for the biosynthesis of auxin (aux),
cytokinin (cyt) and opine (ocs), and is flanked by left and right
borders.
T-DNA borders- A set of 24 kb sequences present on either side (right & left) of T-
DNA are also transferred to the plant cells.
It is clearly established that the right border is more critical for T-DNA transfer.
2. Virulence region: The genes responsible for the transfer of T-DNA into host plant
are located outside T-DNA and the region is reffered to as vir or virulence region .
At least nine vir-gene operons have been identified. These include vir A, vir G, vir
B1, vir C1, vir D1, D2, vir D4 and vir E1,E2.
3. Opine catabolism region: This region codes for proteins involved in the uptake
and metabolisms of opines.
Besides the above three there is ori region that responsible for origin of DNA
replication which permit the Ti plasmid to be stably maintain in A. tumefaciens.
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8. The process of T-DNA transfer and it integration into the host plant genome are as
follows:-
1. Signal induction to Agro bacterium:-
The wounded plant cells release certain chemicals-phenolic compounds
and sugars which are recognized as signals by Agro bacterium. The signals induced
result in a sequence of biochemical events in Agro bacterium that ultimately helps in
the transfer of T-DNA of T-plasmid.
2. Attachment of Agro bacterium to plant cells:-
The Agro bacterium attaches to plant cells through polysaccharides,
particularly cellulose fibres produced by the Bacterium. Several chromosomal
virulence (chv) genes responsible for the attachment of bacterial cells to plant cells
have been identified.
3. Production of virulence proteins:-
As the signal induction occurs in the Agro bacterium cells attach to plant
cell, a series of events take place that result in the production of virulence proteins.
To start with, signal induction by phenolics stimulates vir A which in turn activates
(by phosphorylation) vir G. This induces expression of virulence gene of Ti-plasmid
to produce the corresponding virulence proteins (D1,D2,E2,B etc.).
Certain sugars (eg. Glucose, galactose, xylose) that induce virulence genes have been
identified.
T-
DNA
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9. 4. Production of T-DNA strand:-
The right and left borders of T-DNA are recognized by vir D1/vir D2
proteins. These proteins are involved in the production single-stranded T-DNA (ss
DNA), its protection and export to plant cells. The ss T-DNA gets attached to vir D2.
5. Transfer of T-DNA out of Agro bacterium:-
The ss T-DNA –vir D2 complex in association with vir G is exported from
the bacterial cell. Vir B products form the transport apparatus.
6. Transfer of T-DNA into plant cells and integration:-
The T-DNA –vir D2 complex crosses the plant plasma membrane.In the
plant cells, T-DNA gets covered with vir E2. This covering protects the T-DNA from
degradation by nucleases. Vir D2 and vir E2 interact with a variety of plant proteins
which influences T-DNA transport and integration.
The T-DNA – vir D2, vir E2- plant protein complex enters the nucleus through
nuclear pore complex. Within the nucleus, the T-DNA gets integrated into the plant
chromosome through a process referred to illegitimate recombination.
T-
DNA
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11. The ability of Ti plasmid of Agrobacterium to genetically transform plants has been
described. It is possible to insert a desired DNA sequence (gene) into the T-DNA
region (of Ti-plasmid),and then use A. tumefaciens to deliver this gene into the
genome of plant cell.
Some limitations of Ti-plasmid as vector:-
i. Ti-plasmid are large in size (200-800 kb) smaller vectors are preferred for
recombinant experiment.
ii. Absence of unique restriction enzyme sites on Ti plasmids.
iii. The phytohormones (auxin & cytokinin)produced by the plant cells so auxin ,
cytokinin must be removed.
iv. Opine production is transformed plant cells lowers the plant yield so opine
synthesizing genes should be removed.
Ti
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12. There are two types of Ti plasmid vectors are used for genetic transformation of plant
they are cointegrate vector and binary vector.
1. Cointegrate vector:-
In the cointegrate vector system ,the disarmed and modified Ti plasmid combines with an
intermediate cloning vector to produce a recombinant Ti plasmid.
Production of disarmed Ti plasmid:-
The T-DNA genes for hormone biosynthesis are removed. In place of the deleted DNA, a
bacterial plasmid (pBR322) DNA sequence is incorporated.This disarmed plasmid, also referred
to as receptor plasmid,has the basic structure of T-DNA (right &left borders,virulence genes etc.)
necessary to transfer the plant cell.
Construction of intermediate vector:-
The intermediate vector is constructed with the following components.
• A pBR322 sequence DNA homologous to that found in the receptor Ti plasmid.
• A plant transformation marker(PTM):-
• For e.g. a gene coding for neomycine phosphotransferase 2 (npt2).These gene confers
resistance to kanamycin in the plant cells and thus permits their isolation.
•
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A bacterial resistance marker:-
• For e.g. A gene coding for spectinomycin resistance. This gene confers spectinomycin
resistance to recipient bacterial cells and thus permits their selective isolation.
A multiple cloning site (MCS) Where foreign genes can be inserted.
• A co/E1 origin of replication which allows the replication of plasmid in E.coli but not
in agrobacterium.
• An oriT sequence with basis of mobilization (bom) site for the transfer of
intermediate vector from E.coli to Agrobacterium.
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15. The desired foreign gene (target gene) is first cloned in the multiple cloning site of
the intermediate vector. The cloning process is carried out in E.coli, the bacterium
where the cloning is most efficient. The intermediate vector is mated with
Agrobacterium so that the foreign gene is mobilised into the latter. The transformed
Agrobacterium cells will receptors Ti plasmid and intermediate vector are selectibely
isolated when grown on a minimal medium containing spectinomycin. The selection
process becomes easy since E.coli does not grow on a minimal medium in which
Agrobacterium grows. Within the Agrobacterium cells, intermediate plasmid gets
integrated into the receptor Ti plasmid to produce cointegrate plasmid. This plasmid
containing plant transformation marker (eg.npt 2) gene and cloned target gene between
T-DNA borders is transferred to plant cells. The transformed plant cells can be selected
on a medium containing kanamycin when the plant and Agrobacterium cells are
incubated together.
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16. B
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The binary vector system consist of an Agrobacterium strain along with a disarmed Ti
plasmid called vir helper plasmid (the entire T-DNA region including borders deleted
while vir gene is retained). It may be noted that both of them are not physically
linked (or integrated). A binary vector with T-DNA can replicate in E.coli and
Agrobacterium.
The binary vector has following components-:
1. Left and right borders that delimit the T-DNA region.
2. A plant transformation marker (PTM) e.g. npt2 that confers kanamycin resistance in
plant transformed cells.
3. A multiple cloning site (MCS) for introducing target/foreign genes.
4. A bacterial resistance marker e.g. tetracycline resistance gene for selecting binary
vector colonies in E.coli and Agrobacterium.
5. oriT sequence for conjugal mobilization of the binary vector from E.coli to
Agrobacterium.
6. A broad host- range origin of replication such as RK2 that allows the replication of
binary vector in Agrobacterium.
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17. The target (foreign) gene of interest is inserted into the multiple cloning site of the
binary vector.
• In this way, the target gene is placed between the right and left border repeats and
cloned in E.coli.
• By a mating process, the binary vector is mobilised from E.coli to Agrobacterium.
• Now, the virulence gene proteins of T-DNA of the vector into plant cells.
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18. 1. The binary vector system involves only the transfer of a binary plasmid to
Agrobacterium without any integration.
2. This is in contrast to cointegrate vector system wherein the intermediate vector is
transferred and integrated with disarmed Ti plasmid.
3. Due to convenience, binary vectors are more frequently used than cointegrate
vectors.
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19. Agrobacterium – mediated technique is the most widely used for the transformation
of plants and generation of transgenic plants. The important requirements for gene
transfer in higher plants through Agrobacterium mediation are listed.
The explants of the plant must produce phenolic compounds (e.g. autosyringone) for
activation of virulence genes.
Transformed cells/tissues should be capable to regenerate into whole plants.
AGROBACTERIUM-MEDIATED PLANT TRANSFORMATIONS HAVE THE
FOLLOWING BASIC PROTOCOL:-
1. Development of Agrobacterium carrying the cointegrate or binary vector with the
desired gene.
2. Identification of a suitable explant e.g. cells, protoplasts, tissues, calluses, organs.
3. Co-culture of explants with Agrobacterium.
4. Killing of Agrobacterium with a suitable antibiotic without harming the plant tissue.
5. Selection of transformed plant cells.
6. Regeneration of whole plants.
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21. The Ti plasmid is a large conjugative plasmid or megaplasmid of about 200 kb.
Virulence genes are responsible for the transfer of T DNA into the host cell and
integration of T DNA with host genome.
Octopine Ti plasmids produce an opine called octopine (C9H18N4O4).
Nopaline Ti plasmids produces an opine called as nopaline ( C9H16N4O6).
The TDNA is organised in two distinct regions called TL and TR.
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