Microbiology: A Systems Approach PowerPoint to accompany Microbiology: A Systems Approach Cowan/Talaro Chapter 7 Elements of Microbial Nutrition, Ecology, and Growth Copyright The McGraw-Hill Companies, Inc. Permission required for reproduction or display.
Chapter 7 Topics Microbial Nutrition Transport Across the Membrane Environmental Factors Microbial Growth
Table 7.1
Microbial Nutrition Definitions Nutrition Essential nutrient Macronutrient Micronutrient Inorganic nutrient Organic nutrient
Bacteria are composed of different elements and molecules, with water (70%) and proteins (15%) being the most abundant. Table 7.2 Analysis of the chemical composition of an E. coli cell.
Sources of essential nutrients Required for metabolism and growth Carbon source Energy source
Carbon source Heterotroph (depends on other life forms) Organic molecules Ex. Sugars, proteins, lipids Autotroph (self-feeders) Inorganic molecules Ex. CO2
Sources of Essential Nutrients Nitrogen Oxygen Hydrogen Phosphorous Sulfur
Miscellaneous Nutrients Mineral Ions K, Na, Ca, Mg, Z Trace Elements Cu, Co, Ni, Mb, Mn, Si, B, I Growth Factors
Growth factors Essential organic nutrients Not synthesized by the microbe, and must be supplemented Ex. Amino acids, vitamins
Nutritional Types Carbon Source Energy Source Organic – “Hetero” Inorganic – “Auto” Energy Source Light – “Photo” Chemical – “Chemo”
Energy source Photoautotrophs Chemoautotrophs Photoheterotrophs Chemoheterotrophs
Photoautotroph Derive their energy from sunlight Transform light rays into chemical energy Primary producers of organic matter for heterotrophs Primary producers of oxygen Ex. Algae, plants, cyanobacteria
Fig. 4.27b
Chemoautotrophs Carbon Source is Inorganic ( CO2) Two types Chemical Energy can be organic or inorganic Ex. Methanogens, Lithoautotrophs
Methanogens are an example of a chemoautotroph. Fig. 7.1 Methane-producing archaea
Photoheterotrophs Light energy Organic Carbon Source Purple & Green Photosyntheic Bacteria
Fig. 4.28
Chemoheterotrophs Derive both carbon and energy from organic compounds Saprobic decomposers of plant litter, animal matter, and dead microbes Parasitic Live in or on the body of a host
Representation of a saprobe and its mode of action. Fig. 7.2 Extracellular digestion in a saprobe with a cell wall.
Summary of the different nutritional categories based on carbon and energy source. Table 7.3 Nutritional categories of microbes by energy and carbon source.
Transport mechanisms Osmosis Passive Transport Active transport Simple Diffusion Facilitated Diffusion Active transport Endocytosis
Osmosis Diffusion of water through a permeable but selective membrane Water moves toward the higher solute concentrated areas Isotonic Hypotonic Hypertonic
Representation of the osmosis process. Fig. 7.3 Osmosis, the diffusion of water through a selectively permeable membrane
Cells with- and without cell walls, and their responses to different osmotic conditions (isotonic, hypotonic, hypertonic). Fig. 7.4 Cell responses to solutions of differing osmotic content.
Fig. 7.4
Fig. i7.p211a
Diffusion Net movement of molecules from a high concentrated area to a low concentrated area No energy is expended (passive) Concentration gradient and permeability affect movement
A cube of sugar will diffuse from a concentrated area into a more dilute region, until an equilibrium is reached. Fig. 7.5 Diffusion of molecules in aqueous solutions
Facilitated diffusion Transport of polar molecules and ions across the membrane No energy is expended (passive) Carrier protein facilitates the binding and transport Specificity Saturation Competition
Representation of the facilitated diffusion process. Fig. 7.6 Facilitated diffusion
Active transport Transport of molecules against a gradient Requires energy (active) Requires a transport protein sugars, amino acids, organic acids, phosphates and metal ions.
Fig. 7.7a
Fig. 7.7b
Endocytosis Substances are taken in, but are not transported through the membrane. Requires energy (active) Common for eucaryotes Phagocytosis – solid particles Pinocytosis - liquids
Fig. 7.7c
Example of the permease, group translocation, and endocytosis processes. Fig. 7.7 Active transport
Summary of the transport processes in cells. Table 7.4 Summary of transport processes in cells
Environmental Factors Temperature Gas pH Osmotic pressure Other environmental factors Microbial associations
Temperature For optimal growth and metabolism Psychrophile – 0 to 15 °C Psychrotrophs – 20-30°C Mesophile- 20 to 40 °C Thermophile- 45 to 80 °C Hyperthermophiles - > 80° C
Growth and metabolism of different ecological groups based on ideal temperatures. Fig. 7.8 Ecological groups by temperature
Example of a psychrophilic photosynthetic Red snow organism. Fig. 7.9 Red snow
Gas Two gases that most influence microbial growth Oxygen Respiration Oxidizing agent Carbon dioxide
Oxidizing agent Oxygen metabolites are toxic Singlet Oxygen Superoxide Free Radicals Hydrogen Peroxide Hydroxyl Radicals These toxic metabolites must be neutralized for growth
Five categories of bacteria Obligate aerobe Facultative anaerobe Obligate anaerobe Aerotolerant Anaerobes Microaerophiles
Obligate aerobe Requires oxygen for metabolism Possess enzymes that can neutralize the toxic oxygen metabolites Superoxide dismutase and catalase Ex. Most fungi, protozoa, and bacteria
Facultative anaerobe Does not require oxygen for metabolism, but can grow in its presence During minus oxygen states, anaerobic respiration or fermentation occurs Possess superoxide dismutase and catalase Ex. Gram negative pathogens
Obligate anaerobes Cannot use oxygen for metabolism Do not possess superoxide dismutase and catalase The presence of oxygen is toxic to the cell
Aerotolerant Anaerobes Can tolerate oxygen but don’t use it for growth
Microaerophiles Require Oxygen, but only in small amounts Don’t make enough enzymes to detoxify toxic forms of oxygen if they are exposed to normal atmosphere
Anaerobes must grow in an oxygen minus environment, because toxic oxygen metabolites cannot be neutralized. Fig. 7.10 Culturing technique for anaerobes
Thioglycollate broth enables the identification of aerobes, facultative anaerobes, and obligate anaerobes. Reducing Media Fig. 7.11 Use of thioglycollate broth to demonstrate oxygen requirements.
Fig. 7.10b
pH Cells grow best between pH 6-8 Exceptions would be acidophiles (pH 0), and alkalinophiles (pH 10).
Osmotic pressure Halophiles Withstand hypertonic conditions Some requires high salt concentrations Ex. Halobacterium Some can survive high salt conditions but is not required Ex. Staphylococcus aureus
Other factors Radiation- Spores or pigments help withstand UV, infrared Barophiles – withstand high pressures Spores and cysts- can survive dry habitats
Ecological association Influence microorganisms have on other microbes Symbiotic relationship Non-symbiotic relationship
Symbiotic Organisms that live in close nutritional relationship Types Mutualism – both organism benefit Commensalism – one organisms benefits Parasitism – host/microbe relationship
An example of commensalism, where Staphylococcus aureus provides vitamins and amino acids to Haemophilus influenzae. Fig. 7.12 Satellitism, a type of commensalism
Non-symbiotic Organisms are free-living, and do not rely on each other for survival Types Synergism – shared metabolism, not required Antagonism- competition between microorganisms
Interrelationships between microbes and humans Can be commensal, parasitic, and synergistic Normal Microbial Flora are beneficial Mutualistic Ex. E. coli produce vitamin K for the host
Microbial Growth Binary fission Generation time Growth curve Enumeration of bacteria
Binary fission The division of a bacterial cell Parental cell enlarges and duplicates its DNA Septum formation divides the cell into two separate chambers Complete division results in two identical cells
Representation of the steps in binary fission of a rod-shaped bacterium. Fig. 7.13 Steps in binary fission of a rod-shaped bacterium.
Generation time The time required for a complete division cycle (doubling) Length of the generation time is a measure of the growth rate Exponentials are used to define the numbers of bacteria after growth
Representation of how a single bacterium doubles after a complete division, and how this can be plotted using exponentials. Fig. 7.14 The mathematics of population growth
Fig. 7.14b
Growth curve Lag phase Log phase Stationary phase Death phase
Lag phase Cells are adjusting, enlarging, and synthesizing critical proteins and metabolites Not doubling at their maximum growth rate
Log phase Maximum exponential growth rate of cell division Adequate nutrients Favorable environment
Stationary phase Survival mode – depletion in nutrients, released waste can inhibit growth When the number of cells that stop dividing equal the number of cells that continue to divide
Death phase A majority of cells begin to die exponentially due to lack of nutrients A chemostat will provide a continuous supply of nutrients, thereby the death phase is never achieved.
The four main phases of growth in a bacterial culture. Fig. 7.15 The growth curve in a bacterial culture.
Measuring Microbial Growth Direct Methods Plate Counts Direct cell count Automated devices Coulter counter Flow cytometer Indirect Methods Turbidity Spectrophotometer Measure Metabolic Activity
Fig. i7.6
The direct cell method counts the total dead and live cells in a special microscopic slide containing a premeasured grid. Fig. 7.17 Direct microscopic count of bacteria.
A Coulter counter uses an electronic sensor to detect and count the number of cells. Fig. 7.18 Coulter counter
The greater the turbidity, the larger the population size. Fig. 7.16 Turbidity measurements as indicators of growth