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Lecture 3: Bacterial Genetics and Gene Transfer

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Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

Are prokaryotes haploid or diploid? Why?

Back (Answer)

Haploid. Because they (generally) have 1 circular chromosome (0.5-14Mbps)

#2
Front (Question)

What are the two forms of genetic material in prokaryotes

Back (Answer)

Plasmids (extrachromosomal DNA) and chromosome

#3
Front (Question)

What are plasmids?

Back (Answer)

Usually non-essential, small and self replicating, confer a level of adaptive advantage

#4
Front (Question)

What is the nucleoid?

Back (Answer)

Region of cytoplasm containing genetic material

#5
Front (Question)

How are genes packaged in prokaryotic genetic material?

Back (Answer)

More condensed and close together. Grouped into units called OPERONS - which are under control of a single regulatory sequence

#6
Front (Question)

What is an operon and how is it transcribed

Back (Answer)

An operon is a collection of genes all controlled by the same regulatory sequence. An operon is transcribed into a single mRNA molecule encoding several proteins - “POLYCISTRONIC”.

#7
Front (Question)

What does polycistronic mean?

Back (Answer)

A single (mRNA) molecules encoding several proteins

#8
Front (Question)

does prokaryotic mRNA undergo posttranscriptional modification or have introns?

Back (Answer)

No and no

#9
Front (Question)

How is it that transcription and translation are able to act almost simultaneously (coupled) in prokaryotes?

Back (Answer)

Due to the lack of nuclear barrier alongside no posttranslational modifications

#10
Front (Question)

Prokaryotes VS Eukaryotes

Back (Answer)

Polycistronic monocistronic no introns introns no post-trans. mods mods req. for translat. coupled uncoupled

#11
Front (Question)

Why is the prokaryotic genome highly adaptable and quick evolving? Explain what it is.

Back (Answer)

horizontal gene transfer (HGT). The movement of genetic material between two related/unrelated cells. (combined with spontaneous mutations) Opposite of vertical gene transfer

#12
Front (Question)

Outside of direct cell to cell transfer, how else can HGT occur?

Back (Answer)

Transformation Conjugation Transduction

#13
Front (Question)

Give examples of adaptations that are the result of HGT, contributing to bacteria’s rapid ability to evolve

Back (Answer)

• ability to use new substrates as food • antibiotic resistance • detoxifying harmful chemicals (heavy metals, salts…) • virulence

#14
Front (Question)

What is transformation?

Back (Answer)

Direct uptake of extracellular ‘naked’ DNA by bacterial cells. DNA usually comes from nearby degraded cells. Can be in the form of chromosomal fragments or plasmids This DNA can then be degraded for materials for own metabolism or maintain by ingestion in the chromosome or independent replication (plasmids).

#15
Front (Question)

What is “competence”? What are the two types?

Back (Answer)

The physiological state allowing acquisition of exogenous DNA. • Natural • Induced

#16
Front (Question)

What is Natural competence?

Back (Answer)

Genetically encoded capability to uptake and incorporate exogenous DNA. Possess genes encoding machinery for capture, transport, and incorporate into their chromosome.

#17
Front (Question)

How many species are natural competent? Gram + or - bacteria?

Back (Answer)

> 80 species. Including both gram + and - bacteria

#18
Front (Question)

When and by who was natural competence first seen and with what bacteria?

Back (Answer)

1928, Frederick Griffith, Streptococcus pneumoniae strains

#19
Front (Question)

Briefly explain Frederick Griffiths experiment

Back (Answer)

S. pneumoniae has two strains; rough (R) which is non-virulent and smooth (S) which is virulent. Both was injected into mice. R = no death, S = death of mice. Next… Injecting mice with flame killed S lead to NO death, however, injecting mice with both healthy R alongside flame killed S did lead to mice death as the R was transformed to virulence.

#20
Front (Question)

What is induced competence? How is it done?

Back (Answer)

Artificial permeabilization of bacterial cell envelope. • Heat shock (treating with chemicals like CaCl2 before hand) • Electroporation

#21
Front (Question)

What is conjugation?

Back (Answer)

Mechanism of DNA transfer involving direct cell to cell contract via formation of specific structures called CONJUGAL PILI Main transfer mechanism for plasmids

#22
Front (Question)

By who, when, and how was conjugation described?

Back (Answer)

Joshua Lederberg and Edward Tatum in 1946. Noticed E.coli mutant cells with impaired ability to produce some nutrients (autotrophs) were able to produce them after being in contact with other E.coli cells possessing the ability to do so (phototrophs).

#23
Front (Question)

What is the process/mechanism of conjugation?

Back (Answer)

• DONOR (F+) cell produces a pilus attaching to RECEPTORS in RECIPIENT (F-) cell • Pilus then retracts bring the cells closer, establishing a RELAXOME BRIDGE • Plasmid is nicked at specific location called “ORIGIN OF TRANSFERENCE” (oriT). One of its strands transfers through the relaxosome. • After reconsititution of the plasmid, RECIPIENT CELL BECOMES A POTENTIAL DONOR

#24
Front (Question)

What is an “episome”

Back (Answer)

When a plasmid integrates into a chromosome