Bacterial Systematics Flashcards
What is included in taxonomy?
- Grouping (classification)
- Naming (nomenclature)
- Description
The classification of organisms into similar groups.
What are the main differences between bacteria and archaea?
- Bacterial cell walls have peptidoglycan archaeal cell walls do not.
- Bacteria have one (rRNA); archaea have three. In this respect archaea are similar to eukaryotes.
- Bacteria cannot live above 100 degrees Celsius; archaea can thrive in extreme temperatures.
- Bacterial growth is inhibited by antibiotics; archaeal growth is not inhibited by antibiotics.
What is an evolutionary chronometer? Which properties must such a molecule have?
An evolutionary chronometer is a nucleotide sequence (usually) that
can be used to measure the evolutionary separation of two organisms
• Universally distributed across the group chosen for study
• Functionally homologous in each organism studied
• Conserved regions for alignments of adequate length
• Must change (mutate) at ”sufficient” rate
What is sequence alignment?
a way of arranging the sequences of DNA, RNA, or protein to identify regions of similarity that may be a consequence of functional, structural, or evolutionary relationships between the sequences.
List the order of the hierarchy system, from domain to species.
Domain Kingdom Phylum Class Order Family Genus Species
How is “species” defined in microbiology?
A group of strains that among others have same biochemical properties and also essentially
differentiate from other species
a taxonomic category that defines a population of individuals that (1) is monophyletic (descended from a common ancestor), (2) is genomically coherent, (3) is phenotypically coherent, and (4) can be clearly differentiated from other species.
What is the binomial system?
is a formal system of naming species of living things by giving each a name composed of two parts, both of which use Latin or Greek grammatical forms
What is Bergey’s manual?
is the main resource for determining the identity of prokaryotic organisms
Describe PFGE (Pulsed-field gel electrophoresis)
The scientist takes bacterial cells from an agar plate.
The scientist mixes bacterial cells with melted agarose and pours into a plug mold.
The bacterial cells are broken open with biochemicals, or lysed, so that the DNA is free in the agarose plugs.
The scientist loads the DNA gelatin plug into a gel, and places it in an electric field that separates DNA fragments according to their size.
The gel is stained, so that DNA can be seen under ultraviolet (UV) light. A digital camera takes a photograph of the gel and stores the picture in the computer.