Growing Cultures of Aerobic and Anaerobic Bacteria

Under controlled laboratory conditions, it is possible to adjust oxygen concentrations to maximize the growth rate of a particular bacterial species. Because oxy­gen diffuses only slowly into liquid, the concentration of oxygen frequently limits the growth rate of aerobic and facultatively anaerobic bacteria in liquid culture. To supply oxygen for the growth of aerobic micro­organisms and overcome the growth rate limitations caused by low oxygen concentrations, liquid cultures can be agitated at high speed on a shaker table or by an impeller within the culture vessel, or oxygen can be supplied to the culture vessel through forced aeration (FIG. A). Interrupting the supply of oxygen to an actively growing culture for even a brief period of time can lead to anaerobic conditions, in some cases causing a rapid die-off of the bacteria. Some microbial populations can lose viability if a rotary shaker is turned off for only a few minutes, such as may occur when changing flasks on the shaker table.

Whereas aeration enhances the rates of aerobic growth, oxygen must be excluded from the growth medium to permit the growth of obligate and strict anaerobes. This can be accomplished by adding chemicals that react with and remove molecular oxygen from the growth medium. For example, sodium thioglycollate is frequently added to liquid culture media for the growth of anaerobes because it reacts with molecular oxygen, removing free oxygen from solution.

Similarly, the amino acid cysteine and other compounds containing sulfhydryl groups can also be used to scavenge molecular oxygen from a growth medium. For liquid cultures, nitrogen may be bubbled through the medium to remove air and traces of oxygen, and then the culture vessel is sealed tightly to prevent oxygen from reentering.

There are many types of anaerobic culture chambers that can be employed to exclude oxygen from the atmo­sphere (FIG. B). Common forms of anaerobic chambers, such as the Gas Рак system, generate hydrogen, which reacts with the oxygen as a catalyst within the chamber to produce water. Carbon dioxide is also generated in this system to replace the volume of gas depleted by the conversion of oxygen to water. It is also possible to combine several approaches to ensure absolute anaer­obic conditions. In the Hungate roll tube method, after sterilization of a prereduced medium (a medium from which oxygen is excluded by the incorporation of a chemical that scavenges the free oxygen) within a sealed test tube, the medium is rolled during cooling so that the medium covers the inside of the test tube; the medium is then inoculated with a microorganism un­der a stream of carbon dioxide or nitrogen and tightly sealed with butyl rubber stoppers to keep oxygen out; the development of microbial colonies can be seen on the tube surface, and individual cultures can be ob­served without disturbing other cultures.

A rotary shaker is used to maintain aerobic conditions in liquid cultures.

An anaerobic glove box like this may be used to culture anaer­obes.

Дата добавления: 2015-08-05