Microbial Population Growth Flashcards
Why are prokaryotes so dominant?
They have a very fast growth rate (13 min doubling time) = evolve/adapt fast (eg. antimicrobial resistance)
Describe the process of binary fission (going from one cell to two)
- Chromosome replication begins
- One copy of the origin (of replication) is now at each end of the cell
- Replication finishes
- Two daughter cells result
- Prokaryotes reproduce asexually by cell division through the process of binary fission
- Binary fission results in the formation of two cells that are genetically identical
Describe the classic way of growing microbes: “closed” batch culture system
- Refers to a form of cell culturing
- Defined [limited amount] supply of nutrients is provided
- Once used [become limited] cells cannot proliferate
- Standard method of studying microorganisms in a culture
- Dictated by method not shape of flask
Describe the phases of microbial growth (“feast and famine”)
- Lag Phase: length depends on history of inoculum, time required to get biosynthetic reactions running
- Exponential Phase (log phase): cells are active dividing and nothing is limiting for growth. Population is doubling in a constant time interval (under ideal conditions)
- Stationary Phase: cells stop growing and cryptic growth is observed.
Cryptic growth is when organisms survive by consuming lysed cell constituents of other dead cells within the culture. This is not a static population but a dynamic population. There is an equilibrium between growing and dying cells. - Death Phase: cell death. Equilibrium between growing cells and dying cells is skewed towards death.
Are all cells created equal?
No growth actually means death rate and growth rate is in balance
What do prokaryotes need to multiply?
- Carbon source = building bocks for macromolecular synthesis
- Energy source = energy (electrons) to drive anabolic and catabolic reactions in the cell
- Reducing Power = carriers of energy/electrons (NAD+/NADP+)
- Nicotinamide adenine dinucleotide (NAD)H = reduced form
How do prokaryotic cells harvest energy?
Molecules = natural batteries
- Chemical energy stored in bonds
- Broken chemical bonds release energy that can be captured in new bonds (ATP)
- ATP = most common energy currency
- ATP bonds can be broken again later to release that energy
- This reduction (-red) and oxidation (-ox) of couples compounds can be applied to many compounds and forms the basis for ‘redox reactions’
Describe how simple transformations lead to big repercussions in prokaryotic cells
Breakdown:
- The cells take substrates and turns them into products (called catabolism: energy generation)
ATP is used for…
Buildup:
- The monomers (building blocks) are then used to create macromolecules and other cellular constituents (called anabolism: energy consumption)
What are the limitations to pure cultures when studying communities?
Wild-type strain:
- Has all the essential genes
- Can grow by itself
- Can be isolated into pure culture
Auxotroph - an organism that is unable to synthesis one or more essential growth factors, and it will not grow unless factor is provided
- This means that autotrophs cannot be cultured unless we provide limiting factors
- 98% of all the microorganisms sequenced so far lack essential pathways or key genes for the synthesis of amino acids
How do auxotrophs survive in nature?
Cross feeding: also called syntrophy, is when one species gains metabolic products of another species
- Cross feeding allows for survival of auxotrophs by harvesting resources generated by other organisms
- The interactions can benefit one, or both species
- Auxotrophy is common in nature and partially explains our inability to culture most microbes
- Cross feeding can be: Uni-directional or Bidirectional. The ‘food’ the auxotroph gains can be a byproduct of another organism or cooperative with the organism
What is a microbiome and a microbiota?
Microbiome: The complete collection of microorganisms, and their genes, within a particular environment
Microbiota: Individual microbial species in a biome - bacteria, fungi, archaea and viruses
Describe Culture dependent methods and their pros and cons
Culture dependent methods:
- Relies on culturing of microbes in the lab
- Uses pure cultures, or simple (reduced diversity) enrichments
Pros:
- Allows access to pheontype
- Can study one organism at a time
- Can manipulate conditions to see response of organism
Cons:
- Not all organisms can be cultured
- Too many species to grow them all
- Culturing required precise conditions to match microbial needs
- Does not match real world conditions
Describe Culture independent methods and their pros and cons
Culture independent methods:
- Relies predominantly on nucleic acid-based methods. No culturing required.
- Uses sequencing or metabolic profiling to study all microbes in a sample
Pros:
- Allows access to genotype
- Can study many organisms at a time
- Shows communities as they are in nature
- Can target non-culturable organisms
- Provides access to unknown information/species
Cons:
- No pure culture, so no ability to manipulate
- Expensive and complex methods