Ingham Colin J, Sprenkels Ad, Bomer Johan, Molenaar Douwe, van den Berg Albert, van Hylckama Vlieg Johan E T, de Vos Willem M
Top Institute Food and Nutrition, 6703 CT, Wageningen, The Netherlands.
Proc Natl Acad Sci U S A. 2007 Nov 13;104(46):18217-22. doi: 10.1073/pnas.0701693104. Epub 2007 Nov 7.
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 mum, 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 microcolony in 10,000. (iii) In screening for an enzyme-based, nondominant phenotype by the targeted recovery of Escherichia coli transformed with the plasmid pUC18, based on expression of the lacZ reporter gene without antibiotic-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.
通过微工程技术制造了一种小型化、一次性使用的微生物培养芯片,该芯片由具有多达一百万个生长小室的高度多孔陶瓷片制成。这种通用的培养形式,其离散小室小至7×7微米,能够以前所未有的密度培养分离的微生物样本。该芯片已用于微生物学的四种互补应用。(i)作为一种快速活菌计数系统,其动态范围超过10000,偏差程度低,培养效率高。(ii)用于高通量筛选,每10000个中可回收1个荧光微菌落。(iii)通过靶向回收用质粒pUC18转化的大肠杆菌,基于lacZ报告基因的表达而不进行抗生素抗性选择,筛选基于酶的非显性表型。检测β-半乳糖苷酶活性所需的芯片上生物体环境的快速、连续变化的简便性,突出了一个有利特征,该特征也用于筛选宏基因组文库中的相同活性。(iv)基于一种荧光有机磷酸化合物的代谢,对莱茵河水中超过200000个分离株进行高通量筛选,结果回收了22个具有所需表型的微菌落。根据rRNA序列预测,这些分离株包括六个新物种。这四种应用表明,这种简单、易于制造的芯片对微生物培养产生影响的潜力巨大,可能有助于微生物培养、筛选、计数和选择的完全自动化和多重化。