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It is described using terms like brittle, creamy, sticky and dry. Staphylococci are considered to have a creamy consistency, [1]: 173 while some Neisseria species are sticky, and colonies of diphtheroid bacteria and beta-hemolytic streptococci are typically dry. [1]: 167–8 Bacteria that produce capsules often have a slimy (mucoid) consistency.
Negative selection through replica plating to screen for ampicillin sensitive colonies. Replica plating is a microbiological technique in which one or more secondary Petri plates containing different solid (agar-based) selective growth media (lacking nutrients or containing chemical growth inhibitors such as antibiotics) are inoculated with the same colonies of microorganisms from a primary ...
The process of colony hybridization: growth of cell colonies, replication on filter, hybridization, and identification of desired colonies. Colony hybridization is a method of selecting bacterial colonies with desired genes through a straightforward cloning and transfer process. [1]
The formation of patterns in the growth of bacterial colonies has extensively been studied experimentally. Resulting morphologies appear to depend on the growth conditions. They include well known morphologies such as dense branched morphology (DBM) or diffusion-limited aggregation (DLA), but much complex patterns and temporal behaviour can be fou
The growth rate is the length of time required to form mature colonies visible without magnification on solid media. Mycobacteria forming colonies visible to the naked eye within seven days on subculture are known as rapid growers, while those requiring longer periods are termed slow growers. [3] Iron uptake
For instance, the bacterial colony is a cluster of identical cells (clones). These colonies often form and grow on the surface of (or within) a solid medium, usually derived from a single parent cell. [2] Colonies, in the context of development, may be composed of two or more unitary (or solitary) organisms or be modular organisms.
Organisms that ferment lactose appear dark/black or green often with "nucleated colonies"—colonies with dark centers. [3] Organisms that do not ferment lactose will appear pink and often mucoid. This culture media is important in medical laboratories by allowing the identification of enteric bacteria microbes in a short period of time. [4]
Therefore, a method for the detection of the insert would be useful for making this procedure less time- and labor-intensive. One of the early methods developed for the detection of insert is blue–white screening which allows for identification of successful products of cloning reactions through the colour of the bacterial colony.