The following sections of this BookRags Literature Study Guide is offprint from Gale's For Students Series: Presenting Analysis, Context, and Criticism on Commonly Studied Works: Introduction, Author Biography, Plot Summary, Characters, Themes, Style, Historical Context, Critical Overview, Criticism and Critical Essays, Media Adaptations, Topics for Further Study, Compare & Contrast, What Do I Read Next?, For Further Study, and Sources.
(c)1998-2002; (c)2002 by Gale. Gale is an imprint of The Gale Group, Inc., a division of Thomson Learning, Inc. Gale and Design and Thomson Learning are trademarks used herein under license.
The following sections, if they exist, are offprint from Beacham's Encyclopedia of Popular Fiction: "Social Concerns", "Thematic Overview", "Techniques", "Literary Precedents", "Key Questions", "Related Titles", "Adaptations", "Related Web Sites". (c)1994-2005, by Walton Beacham.
The following sections, if they exist, are offprint from Beacham's Guide to Literature for Young Adults: "About the Author", "Overview", "Setting", "Literary Qualities", "Social Sensitivity", "Topics for Discussion", "Ideas for Reports and Papers". (c)1994-2005, by Walton Beacham.
All other sections in this Literature Study Guide are owned and copyrighted by BookRags, Inc.
Acridine orange is a fluorescent dye. The compound binds to genetic material and can differentiate between deoxyribonucleic acid (DNA) and ribonucleic acid (RNA).
A fluorescent dye such as acridine orange absorbs the energy of incoming light. The energy of the light passes into the dye molecules. This energy cannot be accommodated by the dye forever, and so is released. The released energy is at a different wavelength than was the incoming light, and so is detected as a different color.
Acridine orange absorbs the incoming radiation because of its ring structure. The excess energy effectively passes around the ring, being distributed between the various bonds that exist within the ring. However, the energy must be dissipated to preserve the stability of the dye structure.
The ring structure also confers a hydrophobic (water-hating) nature to the compound. When applied to a sample in solution, the acridine orange will tend to diffuse spontaneously into the membrane surrounding the microorganisms. Once in the interior of the cell, acridine orange can form a complex with DNA and with RNA. The chemistries of these complexes affect the wavelength of the emitted radiation. In the case of the acridine orange-DNA complex, the emitted radiation is green. In the case of the complex formed with RNA, the emitted light is orange. The different colors allow DNA to be distinguished from RNA.
Binding of acridine orange to the nucleic acid occurs in living and dead bacteria and other microorganisms. Thus, the dye is not a means of distinguishing living from dead microbes. Nor does acridine orange discriminate between one species of microbe versus a different species. However, acridine orange has proved very useful as a means of enumerating the total number of microbes in a sample. Knowledge of the total number of bacteria versus the number of living bacteria can be very useful in, for example, evaluating the effect of an antibacterial agent on the survival of bacteria.
Acridine orange is utilized in the specialized type of light microscopic technique called fluorescence microscopy. In addition, fluorescence of DNA or RNA can allow cells in a sample to be differentiated using the technique of flow cytometry. This sort of information allows detailed analysis of the DNA replication cycle in microorganisms such as yeast.