By Michael J. Leboffe, Burton E. Pierce
This full-color atlas is meant to behave as a complement to introductory microbiology laboratory manuals. it's not designed to exchange them, neither is it meant to interchange real functionality of the options. really, the pictures are provided to aid with the translation of results.
The 3rd version of the Photographic Atlas for the Microbiology Laboratory is among the most sensible promoting microbiology books within the larger schooling industry. The authors have equipped at the good fortune of this publication through making major advancements for the recent version. a few of the alterations for the fourth variation include:
a brand new paintings software designed to extend scholar knowing of vital concepts
a brand new "Introduction" bankruptcy offers context and historical past info for the hot microbiology student
Re-organized content material to mirror the "process" a operating microbiologist might stick with to spot an unknown organism
3 new chapters protecting the 3 domain names: micro organism, Archaea, and Eukarya
New pictures, re-scanned and or re-imaged images and new photomicrographs that fit extra heavily what scholars are inclined to detect within the laboratory
a whole remodel that are supposed to permit the scholar to higher entry the material
This atlas can accompany and increase any Microbiology textbook. it really is designed to be of specific worth to scholars in a laboratory state of affairs and will both accompany a laboratory handbook or, in sure classes, it can be utilized in conjunction with workouts for the Microbiology Laboratory, Fourth variation. to supply scholars with a full-color, cost effectively priced lab guide. 3-hole drilled.
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Additional info for A photographic atlas for the 4th edition microbiology laboratory
Within 30 minutes, the atmosphere inside the jar is less than 1% O2 and between 9 and 13% CO2. A methylene blue (or some other) indicator strip is also placed inside the jar. It will turn blue if exposed to air, thus acting as a control to ensure anaerobic conditions have been produced. Figure 3-41 shows two plates inoculated with the same organisms, but one was incubated anaerobically while the other was incubated aerobically. 3-41 PLATES INCUBATED INSIDE AND OUTSIDE THE ANAEROBIC JAR Both Nutrient Agar plates were inoculated with Staphylococcus aureus (top), The Oxoid CampygenTM sachet works in a simiPseudomonas aeruginosa (right), and Clostridium sporogenes (left).
Mycolic acid is a waxy substance that gives acid-fast cells a higher affinity for the primary stain and resistance to decolorization by an acid alcohol solution. A variety of acid-fast staining procedures are employed, two of which are the Ziehl-Neelsen (ZN) method and the Kinyoun (K) method. These differ primarily in that the ZN method uses heat as part of the staining process, whereas the K method is a “cold” stain. In both protocols, the bacterial smear may be prepared in a drop of serum to help the “slippery” acidfast cells adhere to the slide.
3-29 DIFFUSIBLE PIGMENT OF PSEUDOMONAS AERUGINOSA The blue-green pigment pyocyanin often makes P. aeruginosa easy to identify. 26 ⅷ A Photographic Atlas for the Microbiology Laboratory A 3-30 TWO MIXED SOIL CULTURES ON NUTRIENT AGAR A B These plates show the morphological diversity present in two soil samples. B C 3-31 THREE THROAT CULTURES ON SHEEP BLOOD AGAR A There are probably five different species on this plate. B Note the ␣-hemolysis (darkening of the agar; see page 61 for more information) shown by much of the growth.
A photographic atlas for the 4th edition microbiology laboratory by Michael J. Leboffe, Burton E. Pierce