The micro-Petri dish, a million-well growth chip for the culture and high-troughput screening of microorganisms

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Ingham, C.J. and Sprenkels, A.J. and Bomer, J.G. and Molenaar, D. and Berg, A. van den and Hylckama Vlieg, J.E.T. van and Vos, W.M. de (2007) The micro-Petri dish, a million-well growth chip for the culture and high-troughput screening of microorganisms. Proceedings of the National Academy of Sciences of the United States of America, PNAS, 104 (46). pp. 18217-18222. ISSN 0027-8424

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Abstract:A miniaturized, disposable microbial culture chip has been fabricated by microengineering a highly porous ceramic sheet with up to one million growth compartments. This versatile culture format, with discrete compartments as small as 7 x 7 mu m, allowed the growth of segregated microbial samples at an unprecedented density. The chip has been used for four complementary applications in microbiology. (i) As a fast viable counting system that showed a dynamic range of over 10,000, a low degree of bias, and a high culturing efficiency. (ii) In high-throughput screening, with the recovery of 1 fluorescent microcolonly in 10,000. (iii) In screening for an enzyme-based, non-dominant phenotype by the targeted recovery of Escherichia coli transformed with the plasmid pUC18, based on expression of the lacZ reporter gene without anti biotic-resistance selection. The ease of rapid, successive changes in the environment of the organisms on the chip, needed for detection of beta-galactosidase activity, highlights an advantageous feature that was also used to screen a metagenomic library for the same activity. (iv) In high-throughput screening of >200,000 isolates from Rhine water based on metabolism of a fluorogenic organophosphate compound, resulting in the recovery of 22 microcolonies with the desired phenotype. These isolates were predicted, on the basis of rRNA sequence, to include six new species. These four applications suggest that the potential for such simple readily manufactured chips to impact microbial culture is extensive and may facilitate the full automation and multiplexing of microbial culturing, screening, counting, and selection.
Item Type:Article
Copyright:© 2007 National Academy of Sciences of the United States of America
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Electrical Engineering, Mathematics and Computer Science (EEMCS)
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Link to this item:http://purl.utwente.nl/publications/62102
Official URL:http://dx.doi.org/10.1073/pnas.0701693104
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