To color the bacterial organism by utilization of single stain is referred as simple staining. All colors function admirably on bacteria because of the chromatophores (Bisen, 2014).
History of Bacteria Staining
The recoloring of microscopic organisms or bacteria is actually of the later source than the utilization of colors in histological work, as the methodical investigation of microbes did not start until after 1870 (Conn, 2009).
We frequently utilize fundamental stains to look at microscopic organisms. Fundamental stains, because of their positive charge will tie electrostatically to contrarily charged atoms, for example, numerous polysaccharides, proteins, and nucleic acids. Marginally extraordinary methods must be utilized for getting ready microscopic organisms or bacteria for recoloring relying upon whether the microbes are developing on agar or in soup. In broth, the bacteria are moderately scattered so we need to guarantee that we get an adequate number onto the magnifying lens slide so they’re not very elusive.
Purpose of Staining
Each bacterial (be it shade delivering, shade non-creating on agar plates or in the fluid stock medium) cell is exclusively lackluster and consequently not visible under a light magnifying lens. Along these lines, to empower the individual to imagine its physical components shape, estimate, plan, and so forth the bacterial cells are recolored with particular colors (or stains). In bacteriology (or Microbiology), we make utilization of different recoloring strategies each having a particular arrangement of stains (or colors). Some of them are gram staining, capsule staining, spore staining, PHB staining and etc (Nain, 2016).
History of Gram Staining
Gram staining was originated by Christian Gram in 1884 by utilizing this system, microscopic organisms or bacteria are subdivided by their response to this stain into those which hold it, named Gram-positive, and those which are decolorized, named Gram-negative. The strategy is named after the name of its creator, the Danish researcher Hans Christian Gram (1853–1938), who built up the procedure while working with Carl Friedländer in 1884 in the morgue of the city hospital in Berlin. Gram formulated his procedure, not with the end goal of recognizing one sort of bacterium from another, however, to make microorganisms more unmistakable in recolored areas of lung tissue. He declares his strategy in 1884 and incorporated into his short report the perception that the typhus bacillus did not hold the stain.
Purpose of Gram Staining
Gram stain is presumably a standout amongst the most usually utilized recoloring techniques in the field of microbiology. It is considered the most generally used and most important technique of its field. The purpose of gram staining is to find out the bacterial specimen by verifying gram stain. It is one of the differential stains that are utilized to describe microbes in one of two gatherings: either gram positive microscopic organisms or gram-negative microorganisms.
Gram positive microbes will ordinarily have a more grounded liking for precious stone violet on applying gram’s iodine than the gram-negative cell divider. Being severe, gram’s iodine shapes a complex with gem violet in the stain that has appended all the more firmly to the cell mass of gram positive microbes than that of the gram-negative microorganisms. Though the gram-positive microscopic organisms recolor violet thus of the nearness of a thick peptidoglycan layer in the dividers of their cell, the gram negative microbes recolor red, because of the more slender peptidoglycan layer in their cell divider (a thicker peptidoglycan layer takes into consideration the maintenance of the stain, yet a more slender layer does not) (Anderson, Beveridge and Clark, 1983).