Bacterial genetic recombination can occur through transformation, transduction, or conjugation. Transformation involves DNA uptake from dead bacteria. Transduction involves DNA transfer by bacteriophages. Conjugation involves DNA transfer through cell-to-cell contact via plasmids or sex pili. Plasmids are small extrachromosomal DNA molecules that can replicate independently and be transferred between bacteria. Episomes can exist independently or integrate into chromosomes, and include plasmids, viruses, and transposons.
On the basis of need of specific content of any topic, i prepared a slides of plasmid for needy students. I'm also a student that's why i know how useful a proper presentation for us.
In this presentation, i try to cover some basic knowledge regarding to plasmid. If you like this ppt than please let me know, it gives me a motivation. If you need other topics ppt then write a topic name on comment section. THANK YOU
On the basis of need of specific content of any topic, i prepared a slides of plasmid for needy students. I'm also a student that's why i know how useful a proper presentation for us.
In this presentation, i try to cover some basic knowledge regarding to plasmid. If you like this ppt than please let me know, it gives me a motivation. If you need other topics ppt then write a topic name on comment section. THANK YOU
It is defined simply as a technique to efficiently and stably introduce foreign genes into the genome of target cells.
The insertion of unrelated, therapeutic genetic information in the form of DNA into target cells
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
Transportable elements are DNA Sequences that move from one location in a chromosome to another within the same chromosome or into another chromosome.
These are DNA Sequences that move from one location in a chromosome to another within the same chromosome or into another chromosome.
These are DNA Sequences that move from one location in a chromosome to another within the same chromosome or into another chromosome.
These are also known as “Jumping genes”.
A bacterial plasmid is a short, usually circular, and double-stranded segment of DNA that is found in the cytoplasm separate from the main bacterial chromosome. This presentation contains plasmid features, replication, classification and its uses.
It is defined simply as a technique to efficiently and stably introduce foreign genes into the genome of target cells.
The insertion of unrelated, therapeutic genetic information in the form of DNA into target cells
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
Transportable elements are DNA Sequences that move from one location in a chromosome to another within the same chromosome or into another chromosome.
These are DNA Sequences that move from one location in a chromosome to another within the same chromosome or into another chromosome.
These are DNA Sequences that move from one location in a chromosome to another within the same chromosome or into another chromosome.
These are also known as “Jumping genes”.
A bacterial plasmid is a short, usually circular, and double-stranded segment of DNA that is found in the cytoplasm separate from the main bacterial chromosome. This presentation contains plasmid features, replication, classification and its uses.
Bacterial cells rise their level of genetic diversity and overcome their lack of sexuality by horizontal DNA transfer.
Bacterial conjugation is the transfer of genetic material between bacterial cells by direct cell-to-cell contact or by a bridge-like connection between two cells.
Deep Behavioral Phenotyping in Systems Neuroscience for Functional Atlasing a...Ana Luísa Pinho
Functional Magnetic Resonance Imaging (fMRI) provides means to characterize brain activations in response to behavior. However, cognitive neuroscience has been limited to group-level effects referring to the performance of specific tasks. To obtain the functional profile of elementary cognitive mechanisms, the combination of brain responses to many tasks is required. Yet, to date, both structural atlases and parcellation-based activations do not fully account for cognitive function and still present several limitations. Further, they do not adapt overall to individual characteristics. In this talk, I will give an account of deep-behavioral phenotyping strategies, namely data-driven methods in large task-fMRI datasets, to optimize functional brain-data collection and improve inference of effects-of-interest related to mental processes. Key to this approach is the employment of fast multi-functional paradigms rich on features that can be well parametrized and, consequently, facilitate the creation of psycho-physiological constructs to be modelled with imaging data. Particular emphasis will be given to music stimuli when studying high-order cognitive mechanisms, due to their ecological nature and quality to enable complex behavior compounded by discrete entities. I will also discuss how deep-behavioral phenotyping and individualized models applied to neuroimaging data can better account for the subject-specific organization of domain-general cognitive systems in the human brain. Finally, the accumulation of functional brain signatures brings the possibility to clarify relationships among tasks and create a univocal link between brain systems and mental functions through: (1) the development of ontologies proposing an organization of cognitive processes; and (2) brain-network taxonomies describing functional specialization. To this end, tools to improve commensurability in cognitive science are necessary, such as public repositories, ontology-based platforms and automated meta-analysis tools. I will thus discuss some brain-atlasing resources currently under development, and their applicability in cognitive as well as clinical neuroscience.
Multi-source connectivity as the driver of solar wind variability in the heli...Sérgio Sacani
The ambient solar wind that flls the heliosphere originates from multiple
sources in the solar corona and is highly structured. It is often described
as high-speed, relatively homogeneous, plasma streams from coronal
holes and slow-speed, highly variable, streams whose source regions are
under debate. A key goal of ESA/NASA’s Solar Orbiter mission is to identify
solar wind sources and understand what drives the complexity seen in the
heliosphere. By combining magnetic feld modelling and spectroscopic
techniques with high-resolution observations and measurements, we show
that the solar wind variability detected in situ by Solar Orbiter in March
2022 is driven by spatio-temporal changes in the magnetic connectivity to
multiple sources in the solar atmosphere. The magnetic feld footpoints
connected to the spacecraft moved from the boundaries of a coronal hole
to one active region (12961) and then across to another region (12957). This
is refected in the in situ measurements, which show the transition from fast
to highly Alfvénic then to slow solar wind that is disrupted by the arrival of
a coronal mass ejection. Our results describe solar wind variability at 0.5 au
but are applicable to near-Earth observatories.
(May 29th, 2024) Advancements in Intravital Microscopy- Insights for Preclini...Scintica Instrumentation
Intravital microscopy (IVM) is a powerful tool utilized to study cellular behavior over time and space in vivo. Much of our understanding of cell biology has been accomplished using various in vitro and ex vivo methods; however, these studies do not necessarily reflect the natural dynamics of biological processes. Unlike traditional cell culture or fixed tissue imaging, IVM allows for the ultra-fast high-resolution imaging of cellular processes over time and space and were studied in its natural environment. Real-time visualization of biological processes in the context of an intact organism helps maintain physiological relevance and provide insights into the progression of disease, response to treatments or developmental processes.
In this webinar we give an overview of advanced applications of the IVM system in preclinical research. IVIM technology is a provider of all-in-one intravital microscopy systems and solutions optimized for in vivo imaging of live animal models at sub-micron resolution. The system’s unique features and user-friendly software enables researchers to probe fast dynamic biological processes such as immune cell tracking, cell-cell interaction as well as vascularization and tumor metastasis with exceptional detail. This webinar will also give an overview of IVM being utilized in drug development, offering a view into the intricate interaction between drugs/nanoparticles and tissues in vivo and allows for the evaluation of therapeutic intervention in a variety of tissues and organs. This interdisciplinary collaboration continues to drive the advancements of novel therapeutic strategies.
Comparing Evolved Extractive Text Summary Scores of Bidirectional Encoder Rep...University of Maribor
Slides from:
11th International Conference on Electrical, Electronics and Computer Engineering (IcETRAN), Niš, 3-6 June 2024
Track: Artificial Intelligence
https://www.etran.rs/2024/en/home-english/
This presentation explores a brief idea about the structural and functional attributes of nucleotides, the structure and function of genetic materials along with the impact of UV rays and pH upon them.
Slide 1: Title Slide
Extrachromosomal Inheritance
Slide 2: Introduction to Extrachromosomal Inheritance
Definition: Extrachromosomal inheritance refers to the transmission of genetic material that is not found within the nucleus.
Key Components: Involves genes located in mitochondria, chloroplasts, and plasmids.
Slide 3: Mitochondrial Inheritance
Mitochondria: Organelles responsible for energy production.
Mitochondrial DNA (mtDNA): Circular DNA molecule found in mitochondria.
Inheritance Pattern: Maternally inherited, meaning it is passed from mothers to all their offspring.
Diseases: Examples include Leber’s hereditary optic neuropathy (LHON) and mitochondrial myopathy.
Slide 4: Chloroplast Inheritance
Chloroplasts: Organelles responsible for photosynthesis in plants.
Chloroplast DNA (cpDNA): Circular DNA molecule found in chloroplasts.
Inheritance Pattern: Often maternally inherited in most plants, but can vary in some species.
Examples: Variegation in plants, where leaf color patterns are determined by chloroplast DNA.
Slide 5: Plasmid Inheritance
Plasmids: Small, circular DNA molecules found in bacteria and some eukaryotes.
Features: Can carry antibiotic resistance genes and can be transferred between cells through processes like conjugation.
Significance: Important in biotechnology for gene cloning and genetic engineering.
Slide 6: Mechanisms of Extrachromosomal Inheritance
Non-Mendelian Patterns: Do not follow Mendel’s laws of inheritance.
Cytoplasmic Segregation: During cell division, organelles like mitochondria and chloroplasts are randomly distributed to daughter cells.
Heteroplasmy: Presence of more than one type of organellar genome within a cell, leading to variation in expression.
Slide 7: Examples of Extrachromosomal Inheritance
Four O’clock Plant (Mirabilis jalapa): Shows variegated leaves due to different cpDNA in leaf cells.
Petite Mutants in Yeast: Result from mutations in mitochondrial DNA affecting respiration.
Slide 8: Importance of Extrachromosomal Inheritance
Evolution: Provides insight into the evolution of eukaryotic cells.
Medicine: Understanding mitochondrial inheritance helps in diagnosing and treating mitochondrial diseases.
Agriculture: Chloroplast inheritance can be used in plant breeding and genetic modification.
Slide 9: Recent Research and Advances
Gene Editing: Techniques like CRISPR-Cas9 are being used to edit mitochondrial and chloroplast DNA.
Therapies: Development of mitochondrial replacement therapy (MRT) for preventing mitochondrial diseases.
Slide 10: Conclusion
Summary: Extrachromosomal inheritance involves the transmission of genetic material outside the nucleus and plays a crucial role in genetics, medicine, and biotechnology.
Future Directions: Continued research and technological advancements hold promise for new treatments and applications.
Slide 11: Questions and Discussion
Invite Audience: Open the floor for any questions or further discussion on the topic.
Seminar of U.V. Spectroscopy by SAMIR PANDASAMIR PANDA
Spectroscopy is a branch of science dealing the study of interaction of electromagnetic radiation with matter.
Ultraviolet-visible spectroscopy refers to absorption spectroscopy or reflect spectroscopy in the UV-VIS spectral region.
Ultraviolet-visible spectroscopy is an analytical method that can measure the amount of light received by the analyte.
Richard's aventures in two entangled wonderlandsRichard Gill
Since the loophole-free Bell experiments of 2020 and the Nobel prizes in physics of 2022, critics of Bell's work have retreated to the fortress of super-determinism. Now, super-determinism is a derogatory word - it just means "determinism". Palmer, Hance and Hossenfelder argue that quantum mechanics and determinism are not incompatible, using a sophisticated mathematical construction based on a subtle thinning of allowed states and measurements in quantum mechanics, such that what is left appears to make Bell's argument fail, without altering the empirical predictions of quantum mechanics. I think however that it is a smoke screen, and the slogan "lost in math" comes to my mind. I will discuss some other recent disproofs of Bell's theorem using the language of causality based on causal graphs. Causal thinking is also central to law and justice. I will mention surprising connections to my work on serial killer nurse cases, in particular the Dutch case of Lucia de Berk and the current UK case of Lucy Letby.
THE IMPORTANCE OF MARTIAN ATMOSPHERE SAMPLE RETURN.Sérgio Sacani
The return of a sample of near-surface atmosphere from Mars would facilitate answers to several first-order science questions surrounding the formation and evolution of the planet. One of the important aspects of terrestrial planet formation in general is the role that primary atmospheres played in influencing the chemistry and structure of the planets and their antecedents. Studies of the martian atmosphere can be used to investigate the role of a primary atmosphere in its history. Atmosphere samples would also inform our understanding of the near-surface chemistry of the planet, and ultimately the prospects for life. High-precision isotopic analyses of constituent gases are needed to address these questions, requiring that the analyses are made on returned samples rather than in situ.
2. INTRODUCTION
• Genetic recombination - transfer of DNA from one
organism (donor) to another organism (recipient).
The transferred donor DNA may then be integrated
into the recipient's genetic material by various
mechanisms
• Like mutation, genetic recombination contributes to
genetic diversity of a population, which is the source
of variation in evolution
4. TRANSFORMATION
• Genetic recombination in which a DNA
fragment from a dead, degraded bacterium
enters a competent recipient bacterium and it
is exchanged for a piece of the recipient's
DNA.
• Involves 4 steps
5. 1. A donor bacterium dies and is degraded
The 4 steps in
Transformation
6. 2. A fragment of DNA from the dead donor
bacterium binds to DNA binding proteins on the
cell wall of a competent, living recipient bacterium
7. 3. The Rec A protein promotes genetic exchange
between a fragment of the donor's DNA and the
recipient's DNA
10. Transduction
• Another method by which genetic recombination
takes place in bacteria is Transduction.
• Genetic recombination in which a DNA fragment
is transferred from one bacterium to another by a
bacteriophage.
11. What are Bacteriophages?
• Bacteriophage (phage) are obligate intracellular
parasites that multiply inside bacteria by making use of
some or all of the host biosynthetic machinery (i.e.,
viruses that infect bacteria).
12. Transduction (cont’d)
• There are two types of transduction:
– Generalized transduction: A DNA fragment is
transferred from one bacterium to another by a lytic
bacteriophage that is now carrying donor bacterial
DNA due to an error in maturation during the lytic life
cycle.
– Specialized transduction: A DNA fragment is
transferred from one bacterium to another by a
temperate bacteriophage that is now carrying donor
bacterial DNA due to an error in spontaneous
induction during the lysogenic life cycle
13. Seven steps in Generalised
Transduction
1. A lytic bacteriophage adsorbs to a
susceptible bacterium.
14. 2. The bacteriophage genome enters the
bacterium. The genome directs the
bacterium's metabolic machinery to
manufacture bacteriophage components
and enzymes
15. 3. Occasionally, a bacteriophage head or capsid
assembles around a fragment of donor
bacterium's nucleoid or around a plasmid
instead of a phage genome by mistake.
17. 5. The bacteriophage carrying the donor
bacterium's DNA adsorbs to a recipient
bacterium
18. 6. The bacteriophage inserts the donor
bacterium's DNA it is carrying into the recipient
bacterium .
19. 7. The donor bacterium's DNA is exchanged
for some of the recipient's DNA.
20. Six steps in Specialised
Transduction
1. A temperate bacteriophage adsorbs to a
susceptible bacterium and injects its genome .
21. 2. The bacteriophage inserts its genome into the
bacterium's nucleoid to become a prophage.
22. 3. Occasionally during spontaneous induction, a small piece of
the donor bacterium's DNA is picked up as part of the phage's
genome in place of some of the phage DNA which remains in
the bacterium's nucleoid.
23. 4. As the bacteriophage replicates, the segment of bacterial
DNA replicates as part of the phage's genome. Every phage
now carries that segment of bacterial DNA.
25. 6. The bacteriophage genome carrying the
donor bacterial DNA inserts into the recipient
bacterium's nucleoid.
26. Bacterial Conjugation
• Bacterial Conjugation is genetic recombination in
which there is a transfer of DNA from a living donor
bacterium to a recipient bacterium. Often involves a
sex pilus.
• The 3 conjugative processes
I. F
+
conjugation
II. Hfr conjugation
III. Resistance plasmid conjugation
27. • F+ Conjugation- Genetic recombination in which
there is a transfer of an F+ plasmid (coding only for a
sex pilus) from a male donor bacterium to a female
recipient bacterium.
• Doesn’t include chromosomal DNA.
• Involves a sex (conjugation) pilus.
• Other plasmids present in the cytoplasm of the
bacterium, such as those coding for antibiotic
resistance, may also be transferred during this
process.
I. F+ Conjugation
Process
28. The 4 stepped F+ Conjugation
1. The F+ male has an F+ plasmid coding for a sex
pilus and can serve as a genetic donor
29. 2. The sex pilus adheres to an F- female (recipient).
One strand of the F+ plasmid breaks
30. 3. The sex pilus retracts and a bridge is created
between the two bacteria. One strand of the F+
plasmid enters the recipient bacterium
31. 4. Both bacteria make a complementary strand of the F+ plasmid and
both are now F+ males capable of producing a sex pilus. There was
no transfer of donor chromosomal DNA although other plasmids the
donor bacterium carries may also be transferred during F+
conjugation.
32. II. Hfr Conjugation
• Genetic recombination in which fragments of
chromosomal DNA from a male donor
bacterium are transferred to a female recipient
bacterium following insertion of an F+ plasmid
into the nucleoid of the donor bacterium.
• Involves a sex (conjugation)pilus.
33. 5 stepped Hfr Conjugation
1. An F+ plasmid inserts into the donor bacterium's nucleoid
to form an Hfr male.
34. 2. The sex pilus adheres to an F- female (recipient).
One donor DNA strand breaks in the middle of the
inserted F+ plasmid.
35. 3. The sex pilus retracts and a bridge forms between the
two bacteria. One donor DNA strand begins to enter the
recipient bacterium. The two cells break apart easily so
the only a portion of the donor's DNA strand is usually
transferred to the recipient bacterium.
36. 4. The donor bacterium makes a complementary copy
of the remaining DNA strand and remains an Hfr male.
The recipient bacterium makes a complementary
strand of the transferred donor DNA.
37. 5. The donor DNA fragment undergoes genetic
exchange with the recipient bacterium's DNA. Since
there was transfer of some donor chromosomal DNA
but usually not a complete F+ plasmid, the recipient
bacterium usually remains F-
38. III. RESISTANT PLASMID CONJUGATION
• Genetic recombination in which there is a
transfer of an R plasmid (a plasmid coding for
multiple antibiotic resistance and often a sex
pilus) from a male donor bacterium to a
female recipient bacterium.
• Involves a sex (conjugation) pilus
39. 4 Stepped Resistant Plasmid
Conjugation
1. The bacterium with an R-plasmid is multiple
antibiotic resistant and can produce a sex pilus (serve
as a genetic donor).
40. 2. The sex pilus adheres to an F- female
(recipient). One strand of the R-plasmid breaks.
41. 3. The sex pilus retracts and a bridge is created
between the two bacteria. One strand of the R-
plasmid enters the recipient bacterium.
42. 4. Both bacteria make a complementary strand of
the R-plasmid and both are now multiple
antibiotic resistant and capable of producing a sex
pilus.
43. PLASMIDS
• A plasmid is a small DNA molecule within a cell that
is physically separated from a chromosomal DNA and
can replicate independently.
44. • Plasmids carry genes that may benefit survival of the
organism (e.g. antibiotic resistance), and can
frequently be transmitted from one bacterium to
another (even of another species) via horizontal gene
transfer.
• Plasmids usually are very small and contain additional
information.
45. TYPES OF PLASMIDS
Plasmids are classified :
By their ability to be transferred to other bacteria:
1 . Conjugative plasmids
• The sexual transfer of plasmids to another bacterium
through a pilus.
46. 3 . Mobilisable
• Intermediate class of plasmids
• Mobilizable, and carry only a subset of the genes
required for transfer.
•Can 'parasitise' another plasmid, transferring at high
frequencyin the presence of a conjugative plasmid.
2 . Non-conjugative :
• Non-conjugative plasmids don’t initiate conjugation
• Only be transferred with the help of conjugative
plasmids
47. 2. By function
1. Fertility-(F) plasmids,
They are capable of conjugation (they contains the genes for
the pili).
2. Resistance-(R) plasmids,
Contain gene (s) that can build resistance against one or
several antibiotics or poisons.
3. Col-plasmids,
Contain genes coding for colicines, proteins that can kill
other bacteria.
4. Degradative plasmids,
Able to digest unusual substances, e.g., toluene or salicylic
acid.
5. Virulence plasmids,
Turn a bacterium into a pathogen.
48. EPISOMES
• An episome is a portion of genetic material that can
exist independent of the chromosome at some
times, while at other times is able to integrate into
the chromosome.
• Examples of episomes include :
Insertion sequences and transposons.
Viruses
F factor
49. 1. Tranposons and insertion sequence
• Transposons and insertion sequences are
episomes.
• Also known as mobile genetic elements.
• Capable of existing outside of the chromosome.
• Also designed to integrate into the chromosome
and then move from one cell to another.
• Transposons can carry other genetic material
with them.
50. 2. Viruses
• Viruses are another example of an episome.
• Viruses will integrate their genetic material into the
host chromosome.
3. F factor
• F factor that has integrated into the host
chromosome is known as Hfr.
• Hfr stands for high frequency of recombination.
51. IN SUMMURY
BACTERIAL RECOMBINATION occurs in 3 ways
• Transformation
• Transduction
• Recombination
PLASMIDS :
Autonomously replicating extra chromosomal DNA
EPISOMES:
Piece of genetic material capable of existing independent
of chromosome as well as in integrated form.