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Biol 3400Tortora et al – Chap 4

Functional Anatomy of Prokaryotic and Eukaryotic Cells

I. Introduction

Prokaryotic and eukaryotic cells are similar in a number of ways including Chemically similar – contain macromolecules: Nucleic acids, proteins, lipids and polysaccharides’ Similar metabolic reactions to metabolize food, synthesis proteins and nucleic acids and store energy Contain a membrane, cytoplasm, DNA and ribosomes

Prokaryotic and eukaryotic cells differ in a number of ways (Table 4.2) including

Prokaryotic cells DNA is usually in the form of a single circular dsDNA chromosome and not enclosed in a

membrane DNA is not associated with histones; other proteins are associated with DNA They lack membrane bound organelles Usually divide by binary fission

Eukaryotic cells DNA is usually in the form of multiple linear dsDNA chromosomes found in a membrane

bound nucleus The DNA is consistently associated with chromosomal proteins called histones and with

nonhistone proteins They may have a number of membrane bound organelles, including endoplasmic reticulum,

Golgi complex, lysosomes, vacuoles, mitochondria and chloroplasts Cell division usually involves mitosis

Prokaryotic cells: Archaea (member of Archaeal domain = archaeon) and Bacteria (member of Bacterial domain = bacterium)

Prokaryotic cell structures include the following (Fig. 4.6; Note: Underlined structures are found in all prokaryotic cells): Plasma membrane Cytoplasm Nucleoid region Ribosomes Cell wall (and periplasmic space) Flagellum Pili and Fimbriae Inclusions Gas vacuole Capsule and slime layers Endospores

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Biol 3400Tortora et al – Chap 4

Eukaryotic cells: Protozoa, Fungi and Algae

Eukaryotic cell structures include the following (Fig. 4.22; Note: not all cells possess all of these structures at all times): Plasma membrane Cell wall True nucleus - membrane bound nucleus Ribosomes Membrane bound organelles

chloroplast mitochondrion endoplasmic reticulum vacuoles golgi apparatus lysosomes peroxisomes

Cytoskeleton Flagellum/Cilium

II. Cell Morphology

A. Prokaryotic CellsTwo most common cell shapes coccus (pl. cocci) e.g., bacillus (pl. bacilli) e.g.,

Other shapes include: spirillum (pl. spirilli) e.g., Mycelial – e.g., Actinomycetes Stalked – e.g., Caulobacter, Hypomicrobium Plates Star shape

Some prokaryotes are variable in shape and lack a single characteristic form = pleomorphice.g.,

B. Eukaryotic Cells Highly variable: cell shapes vary in shape from sphere and cylinders to very irregular nerve cells.

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Biol 3400Tortora et al – Chap 4

C. Cell Size Cells come in a variety of sizes & shapes Size limit is set by the logistics required to carry out metabolism

The smallest cells are nanobacteria (diameter of 0.05 to 0.2 µm). Mycoplasmas = 0.2 µm in diameter

What factors constrain the lower size limit of cells? Most bacterial cells are 10 times larger than mycoplasmas (1 to 10 µm in diameter) Eukaryotic cells are typically 10 times larger than bacteria (10 - 100 µm in diameter).

What factors constrain the upper size limit of cells?

Generally prokaryotic cells are smaller than eukaryotic cells. But there are exceptions.

e.g., Epulopiscium fishelsoni size up to 80 x 600 µmThiomargarita namibiensis size up to 750 µm in diameter

Nanochlorum eukaryotum 1 to 2 µm in diameter

Generally cells are microscopic. But there are exceptionsLoligo - Atlantic squid has neurons with axon diameters as large as 1.0 mm. Ostrich egg

III Cell Components

A. Plasma membrane Every cell is surrounded by a plasma membrane (also known as a cytoplasmic or cell membrane) Encloses the cytoplasm This is an important feature distinguishing archaea from bacteria and eukaryotes Membranes are selectively permeable barriers - Why?

What is the function of the plasma membrane?

Fluid mosaic model (Fig 4.14) S.J. Singer and G. Nicolson (1972) Dynamic structure bifacial quality – sidedness 5 – 10 nm thick

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Biol 3400Tortora et al – Chap 4

1. Membrane components

i. Lipids backbone or basic fabric often as a lipid bilayer (amphipathic)

hydrophobic corehydrophilic exterior surfaces

ii. Proteins integral (70 to 80 % of the membrane proteins) peripheral (20 to 30% of the membrane proteins)

Functionso Transport – import and exporto Enzymeso Receptorso Intracellular junctionso Cell to cell recognitiono Metabolic processes

iii. Carbohydrates Usually associated with the outer surface of the membrane

2. Differences between bacterial, eukaryotic and archaeal membranes

i. Bacterial membranes Like eukaryotes, most of the membrane lipids are phospholipids unlike eukaryotes bacteria lack sterols such cholesterol but contain sterol like compounds called

hopanoids. The role of hopanoids is likely similar to steroids – stabilized membranes. Some bacteria may have extensive in folding of the plasma membrane to increase membrane surface

area for the purpose of greater metabolic activity

Glycerol diesters (phospholipids)

o Glycerol bonded to phosphate (negatively charged) and two fatty acids o Linkage between fatty acids and glycerol is an ester linkage

O ||

Ester linkage R-O-C-(CH2)n CH3

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Biol 3400Tortora et al – Chap 4

Environmental conditions affect fatty acid composition of membranes

o Fatty acids are generally unbranched and 16 to 18 carbons longe.g., palmitic acid CH3(CH2)14 COOH

stearic acid - 18 carbons

o Fatty acids may be saturated or unsaturated

Membrane composition also varies with species and these differences can be used to identify bacteria (Fatty acid methyl ester analysis - FAME).

ii. Eukaryotic membraneso generally the same structure as bacterial membranes including phospholipids but differs in the

major lipids: phospholipids, sphingolipids and cholesterol. o Microdomains that differ in protein and lipid composition may be found – lipid rafts – span

membrane and appear to be involved in a variety of cellular processes (e.g., signal transduction and cell movement)

Sterols o compounds consisting of carbon skeleton of 4 interconnected rings o targets for polyene antibiotics - damage cell membraneso Mycoplasmas acquire sterols from eukaryotic cells

iii. Archaeal membranes Many are thought to be “Extremophiles” Membranes are distinctive Phospholipids are not the main structural components Have branched chain hydrocarbons attached to glycerol by ether linkages

Glycerol diethers

Ether linkage R-C-O-C-R

Bilayers o glycerol bound to branched hydrocarbons (e.g., phytanyl) by ether linkageo glycerol diethers

Monolayers o diglycerol tetraether o often found in extreme thermophiles

Phosphate, sulfur and sugar containing groups are attached to the third carbon of glycerol resulting in a polar lipids that are the predominant lipids (70 – 93%) in the membrane

Nonpolar lipids (squalene derivatives) make up the rest of the membranes

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Biol 3400Tortora et al – Chap 4

3. The movement of materials across membranes

Review this material on your own – it is largely review from Biol 1010. You should be familiar with the following

Passive Transport Simple diffusion Facilitated diffusion

o Transporter proteins Osmosis

o Aquaporino Osmotic pressure

Active Transporto Group translocation

B. Cell walls

1. Bacterial cell walls

Functions Define cell shape Protection from osmotic shock (turgor pressure) and toxic substances Point of anchorage for flagella May contribute to pathogenicity Most bacteria have cell walls but there are exceptions – e.g., mycoplasmas Forms a strong, protective layer that is relatively porous, elastic and somewhat stretchable

Gram positive and Gram negative (Fig. 4.13)

Can be differentiated through the Gram stain - an important diagnostic tool. Gram negative Gram positive Gram variable

i. Peptidoglycan (murein) Components a. Polysaccharide 1,4 linkages between N-acetylglucosamine (NAG) and N-acetylmuramic acid (NAM) monomers

(Fig 4.12). Note : N-acetylmuramic acid is found only in Bacteria Polymers 10 to 65 monomers long

...NAM – NAG - NAM - NAG - NAM - NAG...

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Biol 3400Tortora et al – Chap 4

b. Peptide chains

Tetrapeptide chains linked to M residues - composed of unusual amino acids (D- amino acids) – Why? L-alanine D-glutamic acid L-lysine (Gram positive) or diaminopimelic acid (DAP; Gram negative) D-alanine

There are either peptide interbridges (G-G-G-G-G: Gram positive) or direct peptide linkages (Gram negative) between tetrapeptides Results in a strong multilayer sheet or sacculus

Autolysins - enzymes used by the bacteria to recycle, reshape or restructure cell wall

Lysozyme Hydrolyes the 1,4 linkages between M and G monomers

Sources of lysozyme predators tears saliva chicken egg white

spheroplast - partial removal of cell wall

protoplast - complete removal of cell wall

Penicillin Prevents formation of peptides cross linkages between tetrapeptides Penicillin binds to transpeptidase Not effective against bacteria lacking cell walls such as mycoplasmas

ii. Gram positive cell wall Up to 20% of the organism peptidoglycan represents 50-90% of this structure relatively thick (ca. 40 nm – ranges from 20 to 80 nm) a thick peptidoglycan layer is more resistant to desiccation Polysaccharides such as teichoic acids (e.g., glycerophosphate or ribitol phosphate residues –

negatively charged) or teichuronic acids are bonded to the peptidoglycan or plasma membrane lipids

Putative function - bind to cations and regulate movement into and out of the cell- Prevent extensive cell wall lysis

Responsible for cell wall’s antigenicity

e.g., Bacilli, Staphylococci, Streptococci

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Biol 3400Tortora et al – Chap 4

iii. Gram negative cell envelope more complex than Gram positive cell wall

Cell wall thin layer of peptidoglycan (ca. 2 to 7 nm) 1 - 10 % of the cell wall lipoproteins instead of teichoic acids

Outer membrane - lipid bilayer phospholipids proteins - e.g., porins lipoproteins – anchored to peptidoglycan The outer membrane may be linked to the plasma membrane in a number of places lipopolysaccharides (LPS)

composed of i) lipid A, ii) the core polysaccharide and iii) the O polysaccharide side chain. main structural component of outer half of outer membrane believed to aid in creating a

permeability barrier as well as contributes to negative charge of the cell surface. Protects pathogenic bacteria from host defenses The LPS (Lipid A componenet in particular) is frequently toxic to animals and known as

endotoxin (i.e., because it is still attached to cell). O polysaccharide is an antigen that is used to distinguish species of bacteria

The outer membrane is more permeable than the plasma membrane to most small molecules due to the presence of porin proteins

Less permeable than the plasma membrane to hydrophobic and amphipathic molecules - makes cells less susceptible to certain antibiotics.

Keeps periplasmic enzymes from diffusing away.

Periplasmic space (30 - 70 nm wide) Gel-like in consistency due to abundance of proteins

Import region where number of chemical reactions occur: oxidation-reduction reactions osmotic regulation solute transport hydrolysis protein secretion

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Biol 3400Tortora et al – Chap 4

2. Archaeal cell wall No peptidoglycan, in particular lacking in N-acetylmuramic acid May be composed of

Pseudopeptidoglycan – N-acetylglucosamine and N-acetyltalosaminuronic acid linked by 1,3 linkages

Protein or glycoproteins - most common form of cell wall Polysaccharide

NOTE: Some Bacteria and Archaea do not have cell wallse.g., mycoplasma

Thermoplasma

3. Eukaryotic cell wall Like Bacteria and Archaea, not all eukaryotes have cell walls

Algal cell wall Polysaccharides are the major components

e.g., cellulose May contain high concentrations of calcium or silicon - diatoms

Fungi Many contain chitin - polysaccharide consisting of N-acetylglucosamine monomers. Composition is used in classification schemes

e.g., primitive Chytridiomycetes fungal cell walls lack chitin but contain cellulose

Protists Many protists have a pellicle for support – rigid layer of components beneath the plasma membrane. Pellicle is composed of protein

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Biol 3400Tortora et al – Chap 4

C. Layers External to the Cell Wall

Prokaryotes Prokaryotes have a variety of layers outside the cell wall

Functions protection

ingestion dehydration loss of nutrients

attachment pathogenicity

Form thick or thin, rigid or flexible layers depending upon composition Variable composition – glycoproteins and polysaccharides

1. Capsule Rigid – tight matrix that excludes particles protein or polysaccharide

2. Slime layer loosely bound layer – easily deformed

3. Extracellular Polymeric Substance (EPS) glycocalyx that helps cells bind to surfaces and other cells – formation of biofilm

Glycocalyx – term that collectively refers to both capsule and slime layer

3. Surface layer (S-layer) nearly all bacteria and Archaea crystalline protein layer unknown function – may function as permeability or protective barrier

D. Genetic InformationDeoxyribonucleic acid (DNA) - macromolecule consisting of nucleotide monomers Backbone = 5'...-Phosphate-Sugar-Phosphate-Sugar -Phosphate-Sugar-…3'

Nucleotide = nucleoside plus phosphate

Nucleoside = deoxyribose + nitogenous base

Purines – adenine & guanine

Pyrimidines - cytosine & thymine

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Biol 3400Tortora et al – Chap 4

Review structure of DNA – Chapter 2

1. Bacterial and Archaeal DNA These organisms do not have a nucleus – the bulk of the genetic material is found in the nucleoid

region

Chromosome single double stranded DNA molecule in the form of a covalently closed circular chromosome –

also known at the genophore Exceptions : Borrelia burgdorferi and some Streptomyces spp. have a linear chromosome;

Rhodobacter sphaeroides has two circular chromosomes

usually only one chromosome and it may be present as multiple copies in rapidly growing cells

DNA arranged into supercoiled domains that are stabilized with structural proteins

In some Archaea – DNA is extensively complexed with proteins that closely resemble histone proteins of eukaryotic organisms

Plasmids autonomously replicating units that usually contain only a few genes (< 30; 1 – 5% of the size of the

chromosome). Most the bacterial and archaeal genomes sequenced contain plasmids Usually covalently closed circles (CCC) but may be linear May contain one to many plasmids Range in size from several kbp to Mbp

Examples of plasmid coded factors (Table 3.3)1. R-plasmids - antibiotic resistance genes2. Bacteriocins3. Conjugal factors 4. Metabolic factors - substrate utilization or fixation5. Virulence factors - toxin production

2. Eukaryotic DNA Most possess a nucleus that contains the bulk of the genetic material Nucleus contains a number of linear chromosomes Chromosomes composed of DNA complexed with protein chromatin DNA associated with Histones in structural subunits called nucleosomes

Chloroplasts and mitochondria also contain small circular genomes

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Biol 3400Tortora et al – Chap 4

E. Ribosomes Sites of protein synthesis Approximately 20 - 25 nm in diameter Large numbers may be present in cells (>10,000 in bacterial cells and more in eukaryotic cells) Number varies depending on the level of protein synthesis going on in the cell.

Bacteria and EukaryaArchaea

Ribosome 70 S* 80S

Large subunit 50 S 60S23S rRNA and 5S rRNA 25 - 28S rRNA and 5.8S rRNA Large number of proteins Large number of proteins

e.g., 34 proteins in E. coli

Small subunit 30S 40S16S rRNA 18S rRNALarge number of proteins Large number of proteins

e.g., 21 proteins in E. coli* Svedberg units (S)

Eukaryotic organisms have 70S ribosomes in their mitochondria and chloroplasts Implications in the endosymbiotic theory

Practical implications of ribosome structural differences

Antibiotic treatment

chloramphenicol all bind 70S bacterial tetracycline ribosomes and disrupt protein kanamycin synthesiserythromycinstreptomycin

diptheria toxin bind 70S archaeal and 80S eukaryotic ribosomes and anisomycin disrupts protein synthesis

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Biol 3400Tortora et al – Chap 4

F. Cytoskeleton

Prokaryotic Cells For many years it was thought that prokaryotic cells lacked cytoskeletal elements. Recently homologues

have been discovered for all three elements of the eukaryotic cytoskeletone.g., FtsZ – tubulin homologue; widely observed in Bacteria and Archaea

MreB – actin homologue; Many rod shaped cellsCrescentin – intermediate filament proteins; Caulobacter

Eukaryotic Cells Have a well developed three dimensional network of fibrous proteins (microtubules, microfilaments and

intermediate filaments Microtubules and microfilaments are very dynamic structures – can be quickly disassembled and

assembled elsewhere

Functions Support Maintenance of cell shape Cell movement - e.g., muscle cell contraction, amoeboid movement, cilia Cell division (mitosis, cytokinesis and meiosis) Cell wall deposition Provides spatial organization and movement of organelles and cytosolic enzymes Regulation of biochemical activities in the cell – mechanical signaling

Cytoskeleton components

a) Microtubules thickest cytoskeletal elements - hollow rods - 25 nm found in the cytoplasm of all eukaryotes composed to and tubulin dimers readily assembled and disassembled grow by addition of subunits to ends centrosome - microtubule organizing centre (MOC) important in cell division a pair of centioles (9 sets of microtubule triplets) often found in the centrosome region of animal

cells. Replicate during cell division. May function in cell division but not necessary as they are generally not found in plant cells.

Functions compression resisting function cell motility (flagella and cilia) chromosome movement organelles movement cell shape

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Biol 3400Tortora et al – Chap 4

b) Microfilaments thinnest cytoskeletal element - 7 nm in diameter composed of protein called actin readily assembled and disassembled

Functions tension bearing function muscle contraction (myosin motors molecules-burn ATP) cytoplasmic streaming (myosin motors molecules-burn ATP) cell motility (pseudopodia) cell division cell shape – three dimensional network just inside the plasma membrane

c) Intermediate filaments 8 to 12 nm in diameter diverse class composed of different protein subunits including keratins more permanent structures not readily assembled and disassembled like microtubules and

microfilaments

Functions tension bearing function maintenance of cell and organelle shape e.g. nuclear lamina fixing positions of certain organelles

G. Motility

Bacterial and Archaeal Movement

1. Flagellum (pl. flagella) one to many flagella up to 60 cell lengths/s

Atrichous – no flagellaMonotrichous - single polar flagellumAmphitrichous - single flagellum at each poleLophotrichous - polar tuft of flagellaPeritrichous - multiple flagella disgributed over the entire cell

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Biol 3400Tortora et al – Chap 4

Parts of a prokaryotic flagellum (Fig 4.8)i. filament - whiplike extension that rotates - helical in shape – 15 to 20 µm long

composed of flagellin – highly conserved in bacteria

ii. curved hook - single protein - connects filament to motor

iii. Basal apparatus or motor composed of many proteins (~30) central rod a series of rings embedded in the cell wall, plasma membrane and outer membrane (Gram negative cells). This structure is around 20 nm in diameter

Mot proteins drive the flagellar motor - energy comes from proton motive force (about 1000 H+/rotation)

Fli proteins act as a switch

> 40 genes (fla, fli, flg) required for synthesis and motility (structural, export of components and timing of synthesis)

2. Gliding cells glide along a surface. Mechanism is unknown but there are several models

a) excreted slime adheres to surface pulls cells along - cyanobacteriab) movement of surface proteins - Flavobacterium

3. Gas Vesicles confer buoyancy on cells and allow to move up and down in a water column composed of two types of protein (97% of the gas vacuole is composed of GvpA (-sheets). The

remainder is made of GvpC (-helix) that acts like a cross linker between the GvpA molecules

4. Behavioural Responses to Stimuli In a heterogenous environment prokaryotes are capable of movement (taxis; pl. taxes) towards or

away from stimuli (light, heat, chemicals and electricity)

Chemotaxis movement towards or away from a chemical stimulus (chemoattractant or chemorepellent). Respond to temporal gradient Respond to very low levels of some materials – 10-8 M for some sugars

Types of Taxesphototaxis - light stimulus

scotophobotaxis - entering darkness has a negative effect on a cell

geotaxis - gravitational stimulimagnetotaxis - magnetic stimuliaerotaxis – oxygen stimulus

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Biol 3400Tortora et al – Chap 4

osmotaxis – high osmotic strength stimulus

Bacteria lack spatial sensing capabilities- they are too small to sense a gradient along the cell length. Consequently they respond in a temporal fashion.1. Periodically sample environment e.g., chemoreceptors – sensory proteins2. Process information through a signal transduction pathway3. Control of direction of flagella rotation

Movement is through a series of a) alternating runs (straight line movement- counterclockwise rotation of flagella) and tumbles (reversal of

direction of flagella rotation) b) The direction of the next run is random; however, if there is a gradient of a chemical attractant or

repellent present, the random movements become biased If the organisms sense an increase in attractant concentration then this results in longer runs and

tumbles are less frequent. This is also the case if the cell senses a decrease in repellant concentration

Eukaryote Movement Cilia and flagella are the most prominent structures for movement

Cilia (sing. - cilium) and Flagella (singl. - flagellum) are composed of microtubules

Cilia and flagella are 0.25 µm in diameter A plasma membrane encases a core of microtubules arranged in the 9 + 2 pattern (Fig 4.23): and

outer ring of 9 evenly spaced doublets around 2 two single microtubules radial spokes and cross-linking proteins connect the microtubules; dynein arms (named after the protein composing these structures) connect microtubules anchored to cell by a basal body - identical in structure to centrioles chemical energy required for movement

Comparison of Flagella and CiliaLength Number Movement

Cilia 2 - 20 µm large number back and forth - rowing(100-1000’s)

Flagella 10 - 200 µm 1 to several undulating or snakelike(sperm cell)

The eukaryotic flagellum is much different in structure than prokaryotic flagella (Another difference between Prokaryotes and Eukaryotes!)

H. Attachment Structures of Prokaryotes

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Biol 3400Tortora et al – Chap 4

Glycocalyx – discussed already

Pili and/or Fimbriae hair like proteinaceous projections used as attachment structures

fimbriae Slender tubes (3 – 10 nm in diameter) composed of helically arranged protein subunits function in attachment and twitching movement more numerous than pili

pili generally longer and thicker than fimbriae but fewer in number attachment between mating bacterial cells consist of phosphate-carbohydrate-protein (single type of pilin) F pilus - important structure involved in bacterial mating (conjugation) which is carried exclusively

by the donor cell

I. Inclusion bodies of Prokaryotes

Storage of energy or structural compounds Often form in response to excess or imbalance in nutrients that are available Usually bounded by a thin non-unit membrane

examples phosphate – polyphosphate – metachromacit granules sulfur glycogen or starch poly--hydroxyalkanoates (e.g., poly--hydroxybutyric acid - PHB) are common carbon reserves

produced by Bacteria and Archaeae.g., B. thuringienisis

YPD mediium – very rich medium – PHBNA medium – spore formation

J. Spores

Functions• reproduction• dispersal - fungi and some actinomycetes produces spores that are readily dispersed• survival under adverse conditions

1. Bacterial endospore

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Biol 3400Tortora et al – Chap 4

Differentiated cells Formed within the cell – refractile body Dormant structures that are highly resistant to heat, desiccation, UV irradiation, chemical

disinfectant – Not a reproductive structure Found commonly in soil Contains little water Complex multilayer spore coat contains peptidoglycan and calcium dipicolinate (required for heat

reistance) in its core

Endospore producing bacteria - at least 16 genera, including Bacillus Clostridium Sporosarcina Oscillospira Desulfotomaculum

i) Endospore Structure

Exosporium thin delicate proteinaceous covering

Spore coat several protein layers Impermeable and responsible for spores resistance to chemicals

Cortex up to half the spore volume peptidoglycan (less cross linked than vegetative cell)

Core or spore wall c) usual cell wall

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Biol 3400Tortora et al – Chap 4

Spore core plasma membrane, cytoplasm, nucleoid energy supply phosphoglycerate contains Ca2+ complexed with dipicolinic acid 10 – 30 % water content of vegetative cells – water moves freely in and out of endospores heat resistance of endospore is determined by state and amount of water in core pH is one unit lower than vegetative cells contains small acid-soluble spore proteins (SASP) which bind DNA and protect it from damage due

to UV, heat and desiccation. May also serve as a carbon and energy source during germination Ca2+ dipicolinic acid complexes and SASP form a gel in cytoplasm – gel like material excludes water

from the endospore protoplasm Low metabolic activity, no macromolecule synthesis and few or no mRNA molecules The core also contains DNA repair enzymes that repair the the DNA once the spore germinates

ii Sporulation (sporogenesis) a very complex inducible process and is controlled by > 200 sporulation specific genes. triggered by environmental conditions which are unfavourable for vegetative growth. In Bacillus

species C, N or P limitation. a multistage process (seven stages have been described for Bacilli) that can last up to 8 hours or

more. Vegetative cell or mother cell becomes compartmentalized forming a spore compartment through invagination of the plasma membrane (sporangium).

Endospores dormant for many years

If conditions become favourable for vegetative growth then the endospore can rapidly convert back to a vegetative cell.

Three stagesi) Activation prepares endospore for germination reversible process treatments like heating conditions endospore to germinate when placed in a nutrient solution

ii) Germination breaking of an endospore’s dormant state, germinants - such as glucose and certain amino acids may

induce gemination characterized by

loss of refractility loss of resistance to heat and chemicals loss of Ca dipicolinate and cortex components, and degradation of SASPs and increased ability to be stained by dyes

iii) Outgrowth develops into a vegetative cell uptake of water swelling macromolecule synthesis vegetative growth until encounters environmental triggers again

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Biol 3400Tortora et al – Chap 4

K. Additional Features of Eukaryotic Cells

Review cell structures and concepts including Endomembrane system and all of its components Mitochondria Chloroplast Endosymbiotic theory – eukaryotic cells arose from larger cells engulfing smaller cells

Mitochondria and chloroplasts contain DNA – closed covalently circular form contain their own ribosomes – 70 S protein synthesis in these organelles is affected by antibiotics such as streptomycin that also kill

or inhibit bacteria rRNA sequences of mtDNA and cpDNA are more closely related to bacteria rRNA

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