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The bacterial DNA is not packaged using histones to form chromatin as in eukaryotes but instead exists as a highly compact supercoiled structure, the precise nature of which remains unclear. [6] Most bacterial chromosomes are circular, although some examples of linear chromosomes exist (e.g. Borrelia burgdorferi). Usually, a single bacterial ...
L-form bacteria, also known as L-phase bacteria, L-phase variants or cell wall-deficient bacteria (CWDB), are growth forms derived from different bacteria. They lack cell walls . [ 1 ] Two types of L-forms are distinguished: unstable L-forms , spheroplasts that are capable of dividing, but can revert to the original morphology, and stable L ...
The bacterial cell wall differs from that of all other organisms by the presence of peptidoglycan (poly-N-acetylglucosamine and N-acetylmuramic acid), which is located immediately outside of the cytoplasmic membrane. Peptidoglycan is responsible for the rigidity of the bacterial cell wall and for the determination of cell shape. It is ...
Like all other organisms, bacteria contain ribosomes for the production of proteins, but the structure of the bacterial ribosome is different from that of eukaryotes and archaea. [69] Some bacteria produce intracellular nutrient storage granules, such as glycogen, [70] polyphosphate, [71] sulfur [72] or polyhydroxyalkanoates. [73]
Klebsiella bacteria tend to be rounder and thicker than other members of the family Enterobacteriaceae. They typically occur as straight rods with rounded or slightly pointed ends. They can be found singly, in pairs, or in short chains. Diplobacillary forms are commonly found in vivo. [6]
structure summary A colicin is a type of bacteriocin produced by and toxic to some strains of Escherichia coli . [ 1 ] Colicins are released into the environment to reduce competition from other bacterial strains .
These structures are invaginations of the plasma membrane observed in gram-positive bacteria that have been chemically fixed to prepare them for electron microscopy. [2] They were first observed in 1953 by George B. Chapman and James Hillier, [3] who referred to them as "peripheral bodies." They were termed "mesosomes" by Fitz-James in 1960. [4]
The bacteria may also enter a symbiotic relationship with certain plants. In such a relationship, the bacteria do not respond to the availability of nitrogen, but to signals produced by the plant for heterocyst differentiation. Up to 60% of the cells can become heterocyst, providing fixed nitrogen to the plant in return for fixed carbon. [6]