Foundations in Microbiology

Seventh Edition

Chapter 9

Microbial Genetics

Lecture PowerPoint to accompany

Talaro

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9.1 Genetics and Genes

Genetics – the study of heredity

The science of genetics explores:

1. Transmission of biological traits from parent to offspring

2. Expression and variation of those traits

3. Structure and function of genetic material

4. How this material changes

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Levels of Structure and Function of the Genome

• Genome – sum total of genetic material of a cell (chromosomes + mitochondria/chloroplasts and/or plasmids)– Genome of cells – DNA– Genome of viruses – DNA or RNA

• DNA complexed with protein constitutes the genetic material as chromosomes

• Bacterial chromosomes are a single circular loop• Eukaryotic chromosomes are multiple and linear

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Figure 9.2

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Chromosome is subdivided into genes, the fundamental unit of heredity responsible for a given trait

– Site on the chromosome that provides information for a certain cell function

– Segment of DNA that contains the necessary code to make a protein or RNA molecule

Three basic categories of genes:1. Genes that code for proteins – structural genes 2. Genes that code for RNA3. Genes that control gene expression – regulatory

genes

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• All types of genes constitute the genetic makeup – genotype

• The expression of the genotype creates observable traits – phenotype

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Genomes Vary in Size

• Smallest virus – 4-5 genes

• E. coli – single chromosome containing 4,288 genes; 1 mm; 1,000X longer than cell

• Human cell – 46 chromosomes containing 31,000 genes; 6 feet; 180,000X longer than cell

Figure 9.3 E. coli cell has spewed out its DNA

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DNA• Two strands twisted into a double helix• Basic unit of DNA structure is a nucleotide• Each nucleotide consists of 3 parts:

– A 5 carbon sugar – deoxyribose– A phosphate group– A nitrogenous base – adenine, guanine, thymine,

cytosine

• Nucleotides covalently bond to form a sugar-phosphate linkage – the backbone– Each sugar attaches to two phosphates –

• 5′ carbon and 3′ carbon

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DNA • Nitrogenous bases covalently bond to the 1′

carbon of each sugar and span the center of the molecule to pair with an appropriate complementary base on the other strand– Adenine binds to thymine with 2 hydrogen bonds– Guanine binds to cytosine with 3 hydrogen bonds

• Antiparallel strands 3′ to 5′ and 5′ to 3′• Each strand provides a template for the exact

copying of a new strand• Order of bases constitutes the DNA code

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Figure 9.4

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Significance of DNA Structure

1. Maintenance of code during reproduction Constancy of base pairing guarantees that the code will be retained

2. Providing variety order of bases responsible for unique qualities of each organism

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DNA Replication• Making an exact duplicate of the DNA involves

30 different enzymes• Begins at an origin of replication• Helicase unwinds and unzips the DNA double

helix• An RNA primer is synthesized at the origin of

replication• DNA polymerase III adds nucleotides in a 5′ to 3′

direction– Leading strand – synthesized continuously in 5′ to 3′

direction– Lagging strand – synthesized 5′ to 3′ in short

segments; overall direction is 3′ to 5′

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• DNA polymerase I removes the RNA primers and replaces them with DNA

• When replication forks meet, ligases link the DNA fragments along the lagging strand to complete the synthesis

• Separation of the daughter molecules is complete

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Figure 9.5

DNA replication is semiconservative because each chromosome ends up with one new strand of DNA and one old strand.

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Figure 9.7 Completion of chromosome replication

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9.2 Applications of the DNA code

• Information stored on the DNA molecule is conveyed to RNA molecules through the process of transcription

• The information contained in the RNA molecule is then used to produce proteins in the process of translation

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Gene-Protein Connection

1. Each triplet of nucleotides on the RNA specifies a particular amino acid

2. A protein’s primary structure determines its shape and function

3. Proteins determine phenotype. Living things are what their proteins make them.

4. DNA is mainly a blueprint that tells the cell which kinds of proteins to make and how to make them

Figure 9.9 DNA-protein relationship

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RNAs

• Single-stranded molecule made of nucleotides– 5 carbon sugar is ribose– 4 nitrogen bases – adenine, uracil, guanine, cytosine– Phosphate

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RNA• 3 types of RNA:

– Messenger RNA (mRNA) – carries DNA message through complementary copy; message is in triplets called codons

– Transfer RNA (tRNA) – made from DNA; secondary structure creates loops; bottom loop exposes a triplet of nucleotides called anticodon which designates specificity and complements mRNA; carries specific amino acids to ribosomes

– Ribosomal RNA (rRNA) – component of ribosomes where protein synthesis occurs

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Figure 9.10

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Transcription: The First Stage of Gene Expression

1. RNA polymerase binds to promoter region upstream of the gene

2. RNA polymerase adds nucleotides complementary to the template strand of a segment of DNA in the 5′ to 3′ direction

3. Uracil is placed as adenine’s complement

4. At termination, RNA polymerase recognizes signals and releases the transcript

100-1,200 bases long

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Figure 9.11

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• All the elements needed to synthesize protein are brought together on the ribosomes

• The process occurs in five stages: initiation, elongation, termination, and protein folding and processing

Translation: The Second Stage of Gene Expression

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Figure 9.12

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The Master Genetic Code

• Represented by the mRNA codons and the amino acids they specify

• Code is universal

• Code is redundant

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Figure 9.13

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Figure 9.14

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• Ribosomes assemble on the 5′ end of an mRNA transcript

• Ribosome scans the mRNA until it reaches the start codon, usually AUG

• A tRNA molecule with the complementary anticodon and methionine amino acid enters the P site of the ribosome and binds to the mRNA

Translation

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Translation

• A second tRNA with the complementary anticodon fills the A site

• A peptide bond is formed• The first tRNA is released and the ribosome

slides down to the next codon• Another tRNA fills the A site and a peptide

bond is formed• This process continues until a stop codon is

encountered

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Translation Termination

• Termination codons – UAA, UAG, and UGA – are codons for which there is no corresponding tRNA

• When this codon is reached, the ribosome falls off and the last tRNA is removed from the polypeptide

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Figure 9.15

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Polyribosomal complex allows for the synthesis of many protein molecules simultaneously from the same mRNA molecule.

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Eukaryotic Transcription and Translation

1. Do not occur simultaneously – transcription occurs in the nucleus and translation occurs in the cytoplasm

2. Eukaryotic start codon is AUG, but it does not use formyl-methionine

3. Eukaryotic mRNA encodes a single protein, unlike bacterial mRNA which encodes many

4. Eukaryotic DNA contains introns – intervening sequences of noncoding DNA – which have to be spliced out of the final mRNA transcript

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Figure 9.17

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Genetics of Animal Viruses

• Viral genome - one or more pieces of DNA or RNA; contains only genes needed for production of new viruses

• Requires access to host cell’s genetics and metabolic machinery to instruct the host cell to synthesize new viral particles

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9.3 Regulation of Protein Synthesis and Metabolism

• Genes are regulated to be active only when their products are required

• In prokaryotes this regulation is coordinated by operons, a set of genes, all of which are regulated as a single unit

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Operons

• 2 types of operons:– Inducible – operon is turned ON by substrate:

catabolic operons - enzymes needed to metabolize a nutrient are produced when needed

– Repressible – genes in a series are turned OFF by the product synthesized; anabolic operon –enzymes used to synthesize an amino acid stop being produced when they are not needed

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Lactose Operon: Inducible Operon

Made of 3 segments:

1. Regulator – gene that codes for repressor

2. Control locus – composed of promoter and operator

3. Structural locus – made of 3 genes each coding for an enzyme needed to catabolize lactose –

-galactosidase – hydrolyzes lactose

permease – brings lactose across cell membrane

-galactosidase transacetylase – uncertain function

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Lac Operon

• Normally off– In the absence of lactose, the repressor binds

with the operator locus and blocks transcription of downstream structural genes

• Lactose turns the operon on– Binding of lactose to the repressor protein

changes its shape and causes it to fall off the operator. RNA polymerase can bind to the promoter. Structural genes are transcribed.

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Figure 9.18

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Arginine Operon: Repressible

• Normally on and will be turned off when the product of the pathway is no longer required

• When excess arginine is present, it binds to the repressor and changes it. Then the repressor binds to the operator and blocks arginine synthesis.

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Figure 9.19

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9.4 Mutations: Changes in the Genetic Code

• A change in phenotype due to a change in genotype (nitrogen base sequence of DNA) is called a mutation

• A natural, nonmutated characteristic is known as a wild type (wild strain)

• An organism that has a mutation is a mutant strain, showing variance in morphology, nutritional characteristics, genetic control mechanisms, resistance to chemicals, etc.

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Figure 9.20

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Causes of Mutations

• Spontaneous mutations – random change in the DNA due to errors in replication that occur without known cause

• Induced mutations – result from exposure to known mutagens, physical (primarily radiation) or chemical agents that interact with DNA in a disruptive manner

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Categories of Mutations

• Point mutation – addition, deletion, or substitution of a few bases

• Missense mutation – causes change in a single amino acid

• Nonsense mutation – changes a normal codon into a stop codon

• Silent mutation – alters a base but does not change the amino acid

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Categories of Mutations

• Back-mutation – when a mutated gene reverses to its original base composition

• Frameshift mutation – when the reading frame of the mRNA is altered

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Repair of Mutations• Since mutations can be potentially fatal, the cell

has several enzymatic repair mechanisms in place to find and repair damaged DNA– DNA polymerase – proofreads nucleotides during

DNA replication– Mismatch repair – locates and repairs mismatched

nitrogen bases that were not repaired by DNA polymerase

– Light repair – for UV light damage– Excision repair – locates and repairs incorrect

sequence by removing a segment of the DNA and then adding the correct nucleotides

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Figure 9.21

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The Ames Test

• Any chemical capable of mutating bacterial DNA can similarly mutate mammalian DNA

• Agricultural, industrial, and medicinal compounds are screened using the Ames test

• Indicator organism is a mutant strain of Salmonella typhimurium that has lost the ability to synthesize histidine

• This mutation is highly susceptible to back-mutation

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Figure 9.22

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Positive and Negative Effects of Mutations

• Mutations leading to nonfunctional proteins are harmful, possibly fatal

• Organisms with mutations that are beneficial in their environment can readily adapt, survive, and reproduce – these mutations are the basis of change in populations

• Any change that confers an advantage during selection pressure will be retained by the population

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9.5 DNA Recombination Events

Genetic recombination – occurs when an organism acquires and expresses genes that originated in another organism

3 means for genetic recombination in bacteria:1. Conjugation

2. Transformation

3. Transduction

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Conjugation

• Conjugation – transfer of a plasmid or chromosomal fragment from a donor cell to a recipient cell via a direct connection– Gram-negative cell donor has a fertility

plasmid (F plasmid, F′ factor) that allows the synthesis of a conjugative pilus

– Recipient cell is a related species or genus without a fertility plasmid

– Donor transfers fertility plasmid to recipient through pilus

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Figure 9.23 (1)

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Figure 9.23 (2)

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Conjugation

• High-frequency recombination – donor’s fertility plasmid has been integrated into the bacterial chromosome

• When conjugation occurs, a portion of the chromosome and a portion of the fertility plasmid are transferred to the recipient

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Figure 9.23 (3)

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Transformation• Transformation – chromosome fragments

from a lysed cell are accepted by a recipient cell; the genetic code of the DNA fragment is acquired by the recipient

• Donor and recipient cells can be unrelated

• Useful tool in recombinant DNA technology

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Insert figure 9.23transformation

Figure 9.24

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Transduction• Transduction – bacteriophage serves as a

carrier of DNA from a donor cell to a recipient cell

• Two types: – Generalized transduction – random fragments of

disintegrating host DNA are picked up by the phage during assembly; any gene can be transmitted this way

– Specialized transduction – a highly specific part of the host genome is regularly incorporated into the virus

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Figure 9.25Generalized transduction

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Figure 9.26Specialized transduction

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Transposons• Special DNA segments that have the

capability of moving from one location in the genome to another – “jumping genes”

• Cause rearrangement of the genetic material• Can move from one chromosome site to

another, from a chromosome to a plasmid, or from a plasmid to a chromosome

• May be beneficial or harmful

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Figure 9.27 Transposons