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GENE TRANSFER IN BACTERIAby
unit 8
GENE TRANSFER IN BACTERIAby
unit 8
GENE TRANSFER IN BACTERIAby
unit 8
GENE TRANSFER IN BACTERIAby
unit 8Subject: Life sciences
Faculty: Ramesh KumarNew Life College of Nursing
Date 08/01/2016
Subject: Life sciences
Faculty: Ramesh KumarNew Life College of Nursing
Date 08/01/2016
GENE TRANSFER IN BACTERIAby
unit 8
GENE TRANSFER IN BACTERIAby
unit 8
GENE TRANSFER IN BACTERIAby
unit 8
GENE TRANSFER IN BACTERIAby
unit 8Subject: Life sciences
Faculty: Ramesh KumarNew Life College of Nursing
Date 08/01/2016
Subject: Life sciences
Faculty: Ramesh KumarNew Life College of Nursing
Date 08/01/2016
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METHODS OF GENE TRANSFERMETHODS OF GENE TRANSFER
DNA transfer by natural methods• 1. Conjugation
• 2. Bacterial transformation
• 3. Retroviral transduction
• 4. Agrobacterium mediated transfer
DNA transfer by natural methods• 1. Conjugation
• 2. Bacterial transformation
• 3. Retroviral transduction
• 4. Agrobacterium mediated transfer
METHODS OF GENE TRANSFERMETHODS OF GENE TRANSFER
DNA transfer by natural methods• 1. Conjugation
• 2. Bacterial transformation
• 3. Retroviral transduction
• 4. Agrobacterium mediated transfer
DNA transfer by natural methods• 1. Conjugation
• 2. Bacterial transformation
• 3. Retroviral transduction
• 4. Agrobacterium mediated transfer
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CONJUGATIONCONJUGATION
• Requires the presence of a special plasmid called the Fplasmid.
• Bacteria that have a F plasmid are referred to as as F+ ormale. Those that do not have an F plasmid are F- of female.
• The F plasmid consists of 25 genes that mostly code forproduction of sex pilli.
• A conjugation event occurs when the male cell extends hissex pilli and one attaches to the female.
• Requires the presence of a special plasmid called the Fplasmid.
• Bacteria that have a F plasmid are referred to as as F+ ormale. Those that do not have an F plasmid are F- of female.
• The F plasmid consists of 25 genes that mostly code forproduction of sex pilli.
• A conjugation event occurs when the male cell extends hissex pilli and one attaches to the female.
CONJUGATIONCONJUGATION
• Requires the presence of a special plasmid called the Fplasmid.
• Bacteria that have a F plasmid are referred to as as F+ ormale. Those that do not have an F plasmid are F- of female.
• The F plasmid consists of 25 genes that mostly code forproduction of sex pilli.
• A conjugation event occurs when the male cell extends hissex pilli and one attaches to the female.
• Requires the presence of a special plasmid called the Fplasmid.
• Bacteria that have a F plasmid are referred to as as F+ ormale. Those that do not have an F plasmid are F- of female.
• The F plasmid consists of 25 genes that mostly code forproduction of sex pilli.
• A conjugation event occurs when the male cell extends hissex pilli and one attaches to the female.
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• This attached pilus is a temporary cytoplasmic bridgethrough which a replicating F plasmid is transferred fromthe male to the female.
• When transfer is complete, the result is two male cells.
• When the F+ plasmid is integrated within the bacterialchromosome, the cell is called an Hfr cell (high frequencyof recombination cell).
• This attached pilus is a temporary cytoplasmic bridgethrough which a replicating F plasmid is transferred fromthe male to the female.
• When transfer is complete, the result is two male cells.
• When the F+ plasmid is integrated within the bacterialchromosome, the cell is called an Hfr cell (high frequencyof recombination cell).
• This attached pilus is a temporary cytoplasmic bridgethrough which a replicating F plasmid is transferred fromthe male to the female.
• When transfer is complete, the result is two male cells.
• When the F+ plasmid is integrated within the bacterialchromosome, the cell is called an Hfr cell (high frequencyof recombination cell).
• This attached pilus is a temporary cytoplasmic bridgethrough which a replicating F plasmid is transferred fromthe male to the female.
• When transfer is complete, the result is two male cells.
• When the F+ plasmid is integrated within the bacterialchromosome, the cell is called an Hfr cell (high frequencyof recombination cell).
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TRANSFORMATIONTRANSFORMATION
• transformation is the direct uptake of exogenous DNA from itssurroundings and taken up through the cell membrane .
• Transformation occurs naturally in some species of bacteria,but it can also be effected by artificial treatment in otherspecies.
• Cells that have undergone this treatment are said to becompetent.
• Any DNA that is not integrated into he chromosome will bedegraded.
• transformation is the direct uptake of exogenous DNA from itssurroundings and taken up through the cell membrane .
• Transformation occurs naturally in some species of bacteria,but it can also be effected by artificial treatment in otherspecies.
• Cells that have undergone this treatment are said to becompetent.
• Any DNA that is not integrated into he chromosome will bedegraded.
TRANSFORMATIONTRANSFORMATION
• transformation is the direct uptake of exogenous DNA from itssurroundings and taken up through the cell membrane .
• Transformation occurs naturally in some species of bacteria,but it can also be effected by artificial treatment in otherspecies.
• Cells that have undergone this treatment are said to becompetent.
• Any DNA that is not integrated into he chromosome will bedegraded.
• transformation is the direct uptake of exogenous DNA from itssurroundings and taken up through the cell membrane .
• Transformation occurs naturally in some species of bacteria,but it can also be effected by artificial treatment in otherspecies.
• Cells that have undergone this treatment are said to becompetent.
• Any DNA that is not integrated into he chromosome will bedegraded.
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THE Ti-PLASMIDSTHE Ti-PLASMIDS• A remarkable feature of the Ti plasmid is that, after infection, part of
the molecule is integrated into the plant chromosomal DNA .
• This segment, called the T-DNA, is between 15 and 30 kb in size,depending on the strain.
• T-DNA contains eight or so genes that are expressed in the plant celland are responsible for the cancerous properties of the transformedcells.
• These genes also direct synthesis of unusual compounds, calledopines, that the bacteria use as nutrient.
• A remarkable feature of the Ti plasmid is that, after infection, part ofthe molecule is integrated into the plant chromosomal DNA .
• This segment, called the T-DNA, is between 15 and 30 kb in size,depending on the strain.
• T-DNA contains eight or so genes that are expressed in the plant celland are responsible for the cancerous properties of the transformedcells.
• These genes also direct synthesis of unusual compounds, calledopines, that the bacteria use as nutrient.
THE Ti-PLASMIDSTHE Ti-PLASMIDS• A remarkable feature of the Ti plasmid is that, after infection, part of
the molecule is integrated into the plant chromosomal DNA .
• This segment, called the T-DNA, is between 15 and 30 kb in size,depending on the strain.
• T-DNA contains eight or so genes that are expressed in the plant celland are responsible for the cancerous properties of the transformedcells.
• These genes also direct synthesis of unusual compounds, calledopines, that the bacteria use as nutrient.
• A remarkable feature of the Ti plasmid is that, after infection, part ofthe molecule is integrated into the plant chromosomal DNA .
• This segment, called the T-DNA, is between 15 and 30 kb in size,depending on the strain.
• T-DNA contains eight or so genes that are expressed in the plant celland are responsible for the cancerous properties of the transformedcells.
• These genes also direct synthesis of unusual compounds, calledopines, that the bacteria use as nutrient.
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• The vir (virulence) region of the Ti- plasmid contains thegenes required for the T-DNA transfer process.
• The genes in this region encode the DNA processingenzymes required for excision, transfer and integration of theT-DNA segment.
• The vir (virulence) region of the Ti- plasmid contains thegenes required for the T-DNA transfer process.
• The genes in this region encode the DNA processingenzymes required for excision, transfer and integration of theT-DNA segment.
• The vir (virulence) region of the Ti- plasmid contains thegenes required for the T-DNA transfer process.
• The genes in this region encode the DNA processingenzymes required for excision, transfer and integration of theT-DNA segment.
• The vir (virulence) region of the Ti- plasmid contains thegenes required for the T-DNA transfer process.
• The genes in this region encode the DNA processingenzymes required for excision, transfer and integration of theT-DNA segment.
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Ti-Plasmid mediatedtransfer of gene into a plant
Ti-Plasmid mediatedtransfer of gene into a plant
• The Ti-Plasmid has an innate ability to transmit bacterial DNAinto plant cells.
• The gene of a donor organism can be introduced into the Tiplasmid at the T-DNA region
• This plasmid now becomes a recombinant plasmid.• By Agrobacterium infection, the donor genes can transferred
from the recombinant Ti- Plasmid and integrated into thegenotype of the host plant.
• The Ti-Plasmid has an innate ability to transmit bacterial DNAinto plant cells.
• The gene of a donor organism can be introduced into the Tiplasmid at the T-DNA region
• This plasmid now becomes a recombinant plasmid.• By Agrobacterium infection, the donor genes can transferred
from the recombinant Ti- Plasmid and integrated into thegenotype of the host plant.
Ti-Plasmid mediatedtransfer of gene into a plant
Ti-Plasmid mediatedtransfer of gene into a plant
• The Ti-Plasmid has an innate ability to transmit bacterial DNAinto plant cells.
• The gene of a donor organism can be introduced into the Tiplasmid at the T-DNA region
• This plasmid now becomes a recombinant plasmid.• By Agrobacterium infection, the donor genes can transferred
from the recombinant Ti- Plasmid and integrated into thegenotype of the host plant.
• The Ti-Plasmid has an innate ability to transmit bacterial DNAinto plant cells.
• The gene of a donor organism can be introduced into the Tiplasmid at the T-DNA region
• This plasmid now becomes a recombinant plasmid.• By Agrobacterium infection, the donor genes can transferred
from the recombinant Ti- Plasmid and integrated into thegenotype of the host plant.
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ConclusionConclusion
Transformation
Conjugation
Gene transfer in bacteria
Transformation
Conjugation
Gene transfer in bacteria
ConclusionConclusion
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REFERENCESREFERENCES• Sukharev, S.I., Klenchin, V.A., Serov, S.M., Chernomordik, L.V. & Chizmadzhev, Y.A. (1992). Electroporation• and electrophoretic DNA transfer into cells. The effect of DNA interaction with electropores. Biophys. J., 63 (5):• 1320-1327.• [2] Chu, G., Hayakawa, H. & Berg, P. (1987). Electroporation for the efficient transfection of mammalian cells with• DNA. Nucleic Acids Res., 15 (3): 1311-1326.• [3] Akamatsu, W., Okano, H.J., Osumi, N., Inoue, T., Nakamura, S., Sakakibara, S.I., Miura, M., Matsuo, N.,
Darnell,• R.B. & Okano, H. (1999). Mammalian ELAV-like neuronal RNAbinding proteins HuB and HuC promote• neuronal development in both the central and the peripheral nervous systems. Proc. Natl. Acad. Sci. USA., 96
(17):• 9885-9890.• [4] Osumi, N. & Inoue, T. (2001). Gene transfer into cultured mammalian embryos by electroporation. Methods., 24• Antoni Ivorra, Boris Rubinsky. "Gels with predetermined conductivity used in electroporation of tissue USPTO
Application #: 20080214986 - Class: 604 21 (USPTO)".• Jump upJump up^ Sugar, I.P.; Neumann, E. (1984). "Stochastic model for electric field-induced membrane pores
electroporation". Biophysical Chemistry 19 (3): 211–25. doi:10.1016/0301-4622(84)87003-9. PMID 6722274.• ^ Alberts, Bruce; et al. (2002). Molecular Biology of the Cell. New York: Garland Science. p. G:35. ISBN 978-0-81
• Sukharev, S.I., Klenchin, V.A., Serov, S.M., Chernomordik, L.V. & Chizmadzhev, Y.A. (1992). Electroporation• and electrophoretic DNA transfer into cells. The effect of DNA interaction with electropores. Biophys. J., 63 (5):• 1320-1327.• [2] Chu, G., Hayakawa, H. & Berg, P. (1987). Electroporation for the efficient transfection of mammalian cells with• DNA. Nucleic Acids Res., 15 (3): 1311-1326.• [3] Akamatsu, W., Okano, H.J., Osumi, N., Inoue, T., Nakamura, S., Sakakibara, S.I., Miura, M., Matsuo, N.,
Darnell,• R.B. & Okano, H. (1999). Mammalian ELAV-like neuronal RNAbinding proteins HuB and HuC promote• neuronal development in both the central and the peripheral nervous systems. Proc. Natl. Acad. Sci. USA., 96
(17):• 9885-9890.• [4] Osumi, N. & Inoue, T. (2001). Gene transfer into cultured mammalian embryos by electroporation. Methods., 24• Antoni Ivorra, Boris Rubinsky. "Gels with predetermined conductivity used in electroporation of tissue USPTO
Application #: 20080214986 - Class: 604 21 (USPTO)".• Jump upJump up^ Sugar, I.P.; Neumann, E. (1984). "Stochastic model for electric field-induced membrane pores
electroporation". Biophysical Chemistry 19 (3): 211–25. doi:10.1016/0301-4622(84)87003-9. PMID 6722274.• ^ Alberts, Bruce; et al. (2002). Molecular Biology of the Cell. New York: Garland Science. p. G:35. ISBN 978-0-81
REFERENCESREFERENCES• Sukharev, S.I., Klenchin, V.A., Serov, S.M., Chernomordik, L.V. & Chizmadzhev, Y.A. (1992). Electroporation• and electrophoretic DNA transfer into cells. The effect of DNA interaction with electropores. Biophys. J., 63 (5):• 1320-1327.• [2] Chu, G., Hayakawa, H. & Berg, P. (1987). Electroporation for the efficient transfection of mammalian cells with• DNA. Nucleic Acids Res., 15 (3): 1311-1326.• [3] Akamatsu, W., Okano, H.J., Osumi, N., Inoue, T., Nakamura, S., Sakakibara, S.I., Miura, M., Matsuo, N.,
Darnell,• R.B. & Okano, H. (1999). Mammalian ELAV-like neuronal RNAbinding proteins HuB and HuC promote• neuronal development in both the central and the peripheral nervous systems. Proc. Natl. Acad. Sci. USA., 96
(17):• 9885-9890.• [4] Osumi, N. & Inoue, T. (2001). Gene transfer into cultured mammalian embryos by electroporation. Methods., 24• Antoni Ivorra, Boris Rubinsky. "Gels with predetermined conductivity used in electroporation of tissue USPTO
Application #: 20080214986 - Class: 604 21 (USPTO)".• Jump upJump up^ Sugar, I.P.; Neumann, E. (1984). "Stochastic model for electric field-induced membrane pores
electroporation". Biophysical Chemistry 19 (3): 211–25. doi:10.1016/0301-4622(84)87003-9. PMID 6722274.• ^ Alberts, Bruce; et al. (2002). Molecular Biology of the Cell. New York: Garland Science. p. G:35. ISBN 978-0-81
• Sukharev, S.I., Klenchin, V.A., Serov, S.M., Chernomordik, L.V. & Chizmadzhev, Y.A. (1992). Electroporation• and electrophoretic DNA transfer into cells. The effect of DNA interaction with electropores. Biophys. J., 63 (5):• 1320-1327.• [2] Chu, G., Hayakawa, H. & Berg, P. (1987). Electroporation for the efficient transfection of mammalian cells with• DNA. Nucleic Acids Res., 15 (3): 1311-1326.• [3] Akamatsu, W., Okano, H.J., Osumi, N., Inoue, T., Nakamura, S., Sakakibara, S.I., Miura, M., Matsuo, N.,
Darnell,• R.B. & Okano, H. (1999). Mammalian ELAV-like neuronal RNAbinding proteins HuB and HuC promote• neuronal development in both the central and the peripheral nervous systems. Proc. Natl. Acad. Sci. USA., 96
(17):• 9885-9890.• [4] Osumi, N. & Inoue, T. (2001). Gene transfer into cultured mammalian embryos by electroporation. Methods., 24• Antoni Ivorra, Boris Rubinsky. "Gels with predetermined conductivity used in electroporation of tissue USPTO
Application #: 20080214986 - Class: 604 21 (USPTO)".• Jump upJump up^ Sugar, I.P.; Neumann, E. (1984). "Stochastic model for electric field-induced membrane pores
electroporation". Biophysical Chemistry 19 (3): 211–25. doi:10.1016/0301-4622(84)87003-9. PMID 6722274.• ^ Alberts, Bruce; et al. (2002). Molecular Biology of the Cell. New York: Garland Science. p. G:35. ISBN 978-0-81
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