He took a fluid containing a mixture of bacteria, diluted it with sterile medium, and delivered it into a container of sterile milk by a specially constructed syringe. After incubation, he found that there were single kind of bacteria growing in container identical to their parent cell. In practice, serial dilution method proved to be tedious, difficult and uncertain for routine use. It also proved to be disadvantageous because one could only isolate in pure form the microbes that predominated in the original mixture. Therefore, another promising device needed to be investigated.
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