Biotechnology Unzipped: Promises and Realities (1997)
Joseph Henry Press (JHP)
The views expressed in this book are solely those of the author(s) and do not necessarily reflect the views of the National Academies.
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see how microbial activity changes over time as conditions change, and as cultured bacteria become incorporated into a microbial consortium. Finally, the lux genes signal scientists when the cleanup job is done. Where there are no more toxic molecules to find and degrade, the lights go out.

Finding the right microbes for the job

A great deal of research in environmental biotechnology is devoted simply to finding better ways of measuring and sampling the activities of microbes that might be potentially useful. It can take a lot of time and a lot of highly trained microbiologists to find the right microbes needed, for example, to degrade a particular pollutant. Only after the microbes are found can the task of genetic improvement proceed. To speed things up, many biotech companies are racing to develop more cost-effective and less labor-intensive ways of screening large numbers of bacteria. It's potentially a very lucrative field for those that succeed, as screening is the first step in developing most bioremediation programs.

A simple method recently tested quickly sorts out bacteria able to break down volatile organic compounds, such as carbon tetrachloride (used as cleaning fluid), toluene (an anti-knock agent added to gasoline), or xylene. The method consists of growing cultures of different bacteria on plates containing a dye. Eight dozen different cultures are grown on each plate, and the plates are exposed to chemical vapors in a sealed container. Bacteria that can degrade the contaminating fumes carry out oxidative reactions which, in turn, cause the dye to


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