华中农业大学微生物英文版课件2.ppt

1、Chapter 2 Cell Biology,2.1 Overview of the structure of microbial cells 2.2 Procaryotic cell wall 2.3 Cytoplasmic membrane 2.4 Cellular genetic information 2.5 Cytoplasmic matrix Ribosome and Inclusions 2.6 Components external to the cell wall 2.7 Bacterial endospores 2.8 Comparison of the prokaryot

2、ic and eukaryotic cell,Chapter outline,A procaryotic cell,A eucaryotic cell,Overview of cell structure,3. Their cell wall almost always contain the complex polysaccharide peptidoglycan,The prokaryotic cell,1. Their genetic material (DNA) is not enclosed within a membrane and they lack other membrane

3、 bounded organelles,2. Their DNA is not associated with histidine,4. They are very small!,Size: Most bacteria fall within a range from 0.2 to 2.0 um in diameter and from 2 to 8 um in length,A rod-shaped prokaryote is typically about 1-5 micrometers (m) long and about 1 m wide,Microorganisms in gener

4、al are very small and are completely invisible to the naked eye.,A cyanobacterium 8 x 50 um,size comparison of microorganisms,Visibility scale,Meters,Relative size of Microbes,Prokaryotes,Eukaryotes,Viruses,Naked eye,Light microscope,Electron microscope,a cell increases in size, its surface area to

5、volume ratio decreases,Surface area and volume relationships in cells,spirallum,Shape: Bacteria have a few basic shapes,spherical coccus,Rod-shaped bacillus,The cell wall of the bacterial cell is a complex, semi-rigid structure that is responsible for the characteristic shape of the cell. The cell w

6、all surrounds the underlying, fragile plasma (cytoplasmic) membrane and protects it and internal parts of the cell from adverse changes in the surrounding environment. Almost all prokaryotes have cell walls.,Prokaryotic cell wall,Gram+,Gram-,Schematic diagram of bacterial cell walls,Bacteria can be

7、divided into two major groups, called gram-positive and gram-negative. The original distinction between gram-positive and gram-negative was based on a special staining procedure, the Gram stain,The Gram-positive cell wall has a peptidoglycan layer that is relatively thick (ca. 40 nm) and comprises a

8、pproximately 90% of the cell wall. The cell walls of most Gram-positive eubacteria also have teichoic acids.,Gram-positive cell wall,Structure of the Repeating Unit in Peptidoglycan,These constituents are connected to form a repeating structure, the glycan tetrapeptide.,Peptidoglycan is composed of

9、two sugar derivatives, N-acetylglucosamine (NAG) and N-acetylmuramic acid (NAM), and a small group of amino acids consisting of L-alanine, D-alanine, D-glutamic acid, and either lysine or diaminopimelic acid (DAP).,Peptide and glycan units are connected in formation of the peptidoglycan sheet,Gram-p

10、ositive Bacteria frequently have acidic polysaccharides called teichoic acids attached to their cell wall. The term teichoic acids includes all wall, membrane, or capsular polymers containing glycerophosphate or ribitol phosphate residues. These polyalcohols are connected by phosphate esters and usu

11、ally have other sugars and D-alanine attached.,Teichoic acids,Teichoic acids and lipoteichoic acids are arranged in the overall wall structure of gram-positive Bacteria .,Teichoic acid,Lipoteichoic acid,The Gram-negative cell wall is a thin layer attached to an outer membrane via lipoproteins. The o

12、uter membrane contains phospholipid on its inner surface and lipopolysaccharide (LPS) on its outer surface. The space between the outer membrane and the cytoplasmic membrane is called the periplasmic space.Teichoic acids do not occur in Gram-negative bacterial cell walls.,O side chain,Core polysacch

13、aride,Lipid A,Chemical structure of Lipopolysaccharide,Molecular model of E.coli lipopolysaccharide,The bonds between the carbohydrates in pseudopeptidoglycan are 1-3 instead of1-4 as in peptidoglycan.,CELL WALLS OF ARCHAEBACTERIA,The archaebacteria do not contain peptidoglycan in their cell walls a

14、s occurs in eubacteria.,N-acetylmuramic acid and D-amino acids are not found in the cell walls of archaebacteria.,( Differences from eubacteria ),Some archaebacteria have walls composed of pseudopeptidoglycan, which resembles the peptidoglycan of eubacteria but contains N-acetyltalosaminuronic acid

15、instead of N-acetylmuramic acid and L.-amino acids instead of the D-amino acids in eubacterial cell walls.,Protoplast Formation,Peptidoglycancan be destroyed by certain agents for instance lysozyme, that breaks the 1,4-glycosidic bonds between N-acetylglucosamine and N-acetylmuramic acid in the mole

16、cule.,The difference between gram-positive and gram-negative bacteria is due to the physical nature of their cell walls. If the cell wall is removed from gram-positive bacteria, they become gram negative.,The peptidoglycan seems to act as a permeability barrier preventing loss of crystal violet. Gra

17、m-negative peptidoglycan is very thin, not as highly cross-linked, and has larger pores. Alcohol treatment also may extract enough lipid from the gram negative wall to further increase its porosity. For these reasons, alcohol more readily removes the purple crystal violet-iodine complex from gram-ne

18、gative bacteria.,The Mechanism of Gram Staining,Procedures of Gram Staining,Gram positive or Gram negative?,Morphology of a gram-positive bacterial cell,Structure of cytoplasmic membrane Function of cytoplasmic membrane,2.3 Cytoplasmic membrane,A. The typical cytoplasmic membrane of prokaryotic and

19、eukaryotic cells is a lipid bilayer, as illustrated here showing the orientations of the hydrophilic (tan spheres) and hydrophobic (black) ends of phospholipids that make up this structure. B. Colorized electron micrograph ofthe cytoplasmic membrane (CM) of the bacterium Bacillus subtilis reveals th

20、e characteristic railroad track appearance of this lipid bilayer.,Structure of cytoplasmic membrane,It is a typical UNIT MEMBRANE !,The cytoplasmic membrane, a highly selective barrier, is constructed principally of lipid, within which certain proteins are embedded.,Membranes contain both lipids and

21、 proteins, although the exact proportions of lipid and protein vary widely.,1. Permeability barrier -prevents leakage and function as gate way for transport of nutrients into and out of the cell. 2. Protein anchor- site of many proteins involved in transport, bioenergetics, and chemotaxis. 3. Energy

22、 conservation- site of generation and use of the proton motive force.,Function of membrane,Intracellular membrane system,Bacteria cells dont contain membrane-enclosed organelles. However, bacteria may have specialized invaginations of the cytoplasmic membrane. Their function may be to provide a larg

23、er membrane surface for greater metabolic activity.,Structure of Mesosome,Mesosome may be involved in wall formation during division or play a role in chromosome replication and distribution to daughter cells. It may also be involved in secretory processes,2.4 Cellular genetic information,Bacterial

24、Chromosome Supercoiling and chromosome structure Chromosomal copy number Plasmids,Micrograph of a bacterium showing the nucleoid region (green) within the cytoplasm where the bacterial chromosome occurs,The bacterial chromosome is a circular DNA macromolecule except in Streptomyces where it is linea

25、r and Rhodobacter sphaffoides, which has two separate chromosomes.,Bacterial chromosome,The bacterial chromosome is usually a single covalently closed circular molecule.,The term nucleoid is used to describe aggregated DNA in the prokaryotic cell.,Range of genome sizes in virous groups of organisms

26、and the organellesof eukarya,The bacterial chromosome and supercoiling:,Example of E. coli cell,There are over 50 supercoiled domain in the E.coli chromosome. The total amount of DNA is about 4600 kb. If the total DNA is opened and linearized, it would be 1 mm in length. The the cell is only about 2

27、-3 um long. So to package this much DNA into the cell requires that the DNA be highly supercoiled.,Electron micrograph of an isolated nucleoid released from E.coli.,Chromosome copy number,Bacteria that reproduce asexually are typically haploid in genetic complement. Rapidly growing cells contain mor

28、e than 1 copy of the chromosome, and only when cell growth has ceased does the chromosome number approach one per cell.,Reproduction of a bacterial cell requires the replication of the bacterial chromosome. The micrograph shows the sequence of synthesis of new circular loops of double helical DNA.,B

29、acteria normally reproduce by binary fission. The inward growth of the septum divides the parent cell to produce two equal-sized progeny cells.,Plasmids dont contain the genetic information for the essential metabolic activities of the cell, but they generally do contain genetic information for spec

30、ial features.,Plasmid,Prokaryotic cells have small extra-chromosomal genetic elements called plasmids.,Resistant plasmids Col plasmids Conjugative plasmids Metabolic plasmids,Major types of plasmids,2.5 Cytoplasmic matrix Ribosome and Inclusions,All eucaryotic and procaryotic cells contain ribosomes

31、, which function as the sites of protein synthesis. Ribosomes are composed of two subunits Procaryotic ribosomes are called 70S ribosomes, and those of eucaryotic cells are known as 80S ribosomes,Ribosomes,The letter S refers to Svedberg units, which indicate the relative rate of sedimentation durin

32、g ultra-high-speed centrifugation,Within the cytoplasm of procaryotic (and eucaryotic) cells are several kinds of reserve deposits, known as inclusions. Some inclusions are common to a wide variety of bacteria, whereas others are limited to a small number of species and therefore serve as a basis fo

33、r identification. Among the more prominent bacterial inclusions are the following:,Carbon storage polymers PHB and glycogen Phosphate polymers Sulfur Granules Gas Vacuoles,INCLUSIONS,Polyhydroxybutyric acid (PHB),PHB is a lipidlike compound - one of the most common inclusion bodies in prokaryotic or

34、ganisms. PHB is commonly found as a storage material and unique to bacteria Glycogen is a starchlike polymer of glucose subunits. Glycogen granules are usually smaller than PHB granules.,A Vibrio species,Many microorganisms accumulate granules of polyphosphate, which are large reserves of inorganic

35、phosphates that can be used in the synthesis of ATP,Polyphosphate granule in a bacterial cell,A Pseudomonas species,The sulfur globules inside the cells of purple sulfur bacterium,Chromatium buderi,Some bacteria, including many photosynthetic bacteria, accumulate elemental sulfur granules as a resul

36、t of their metabolism.,Gas vacuoles (blue) and storage granules (red) in the cyanobacterium Microcystis,The formation of gas vacuoles by aquatic bacteria provides a mechanism for adjusting the buoyancy of the cell.Many aquatic cyanobacteria use their gas vacuoles to move up and down in the water col

37、umn.,2.6 Components external to the cell wall,Flagella Fimbriae and pili Capsules and slime layers,Motility allows the cell to reach different regions of its environment. In the struggle for survival, movement to a new location may mean the difference between survival and death of the cell. But, as

38、in any physical process, cell movement is closely tied to an energy expenditure, and the movement of flagella is no exception.,Many prokaryotes are motile, and this ability to move independently is usually due to a special structure, the flagellum (plural, flagella).,Four basic types of flagellar ar

39、rangements,a, monotrichous,b, amphitrichous,c, lophotrichous,d, peritrichous,Flagella are arranged differently on different bacteria. In polar flagellation the flagella are attached at one or both ends of the cell. Occasionally a tuft (group) of flagella may arise at one end of the cell, an arrangem

40、ent called lophotrichous. In peritrichous flagellation the flagella are inserted at many places around the cell surface (peri means around). The type of flagellation, polar or peritrichous, is often used as a characteristic in the classification of bacteria.,The flagellum of a Gram-negative bacteriu

41、m,The filament of bacterial flagella is composed of subunits of a protein called flagellin.,The base of the flagellum is different in structure from that of the filament. There is a wider region at the base of the flagellum called the hook. The hook consists of a single type of protein and functions

42、 to connect the filament to the motor portion of the flagellum.,The basal body is anchored in the cytoplasmic membrane and cell wall. The basal body consists of a small central rod that passes through a system of rings.,In gram-negative Bacteria, an outer ring is anchored in the lipopolysaccharide l

43、ayer and another in the peptidoglycan layer of the cell wall, and an inner ring is located within the cytoplasmic membrane. In gram-positive Bacteria, which lack the outer lipopolysaccharide layer, only the inner pair of rings is present. Surrounding the inner ring and anchored in the cytoplasmic me

44、mbrane are a pair of proteins called Mot . These proteins actually drive the flagellar motor causing a torque that rotates the filament. A final set of proteins, called the Fli proteins function as the motor switch, reversing rotation of the flagella in response to intracellular signals.,The movemen

45、t of a procaryotic flagellum results from rotation of its basal body and is similar to the movement of the shaft of an electric motor. Bacterial cells can alter the speed and direction of rotation of flagella and thus are capable of various patterns of motility.,Fimbriae can be evenly distributed ov

46、er the entire surface of the cell. They can number anywhere from a few to several hundred per cell. Fimbriae allow a cell to adhere to surfaces including the surfaces of other cells.,Pili are usually longer than fimbriae and number only one or two per cell. Pili function to join bacterial cells prio

47、r to the transfer of DNA from one cell to another.,F pilus,Many prokaryotic organisms secrete on their surfaces slimy or gummy materials. A variety of these structures consist of polysaccharide, and a few consist of protein. The terms capsule and slime layer are frequently used to describe polysacch

48、aride layers.,Demonstration of the presence of a capsule is usually by means of negative staining,Capsules and Slime Layers,Many prokaryotes contain a cell surface layer composed of a two-dimensional array of protein. These layers are called S-layers. S-layers have been detected in representatives o

49、f virtually every phylogenetic grouping of Bacteria and are nearly universal among Archaea. In some species of Archaea the S-layer is also the cell wall. The major function of S-layers is unknown. However, as the interface between the cell and its environment it is likely that in cells that produce

50、them the S-layer at least functions as an external permeability barrier, allowing the passage of low-molecular-weight substances while excluding large molecules.,Paracrystalline Surface Layers (S-Layers),2.7 Bacterial endospores,Certain species of bacteria produce special structure called endospores

51、. They are very resistant to heat and can not be destroyed easily, even by harsh chemicals. Endospores are also resistant to other harmful agents such as drying, radiation, acids and chemical disinfectants.,Sporulating cell,Central core,Cortex,Spore coat / membrane,exosporium,Micrograph of a endospo

52、re,Vegetative cell,Containing abundant DPA (dipicolinic acid) which is combined with calcium ions. Lower water content only 10-30% of the water content of the vegetative cell. Low pH value, and contains small acid-soluble spore proteins (SASPs),Structure of DPA,Properties of endospore and its resist

53、ance,Sporulation involves a very complex series of events in cellular differentiation. Bacterial sporulation does not occur when cells are dividing exponentially but only when growth ceases owing to the exhaustion of an essential nutrient. Thus, cells of Bacillus cease vegetative growth and begin sp

54、orulation when a key nutrient such as the carbon or nitrogen source becomes limiting.,Endospore formatiom,1, Axial filament formation 2, Septum formatiom 3, Engulfment of forespore 4, Cortex formation 5, Coat synthesis 6, Completion of coat synthesis, Increase in refractility and heat resistance 7,

55、Lysis of sporangium, spore liberation,Stages in endospore formation,Spore germination 1. Activation Usually results from treatments like heating. 2. Germination Breaks spores dormant state. This process is characterized by spore swelling, loss of resistance to heat and other stresses, loss of refractility and increase in metabolic activity. 3. Outgrowth The spore protoplast makes new components and develops once more into an active bacterium.,Parasporal Crystal (Spore-companioned crystal),Several Bacillus species, most notably B.popilliae and B. thuringiensis, pr