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Biology subjects

Nchinda, N.

Publications and source records attributed to Nchinda, N..

2 recordsLinked to original sources

Surface Patterned Omniphobic Tiles (SPOTs): a versatile platform for scalable liquid handling

Manipulating liquids is a ubiquitous need for experiments across numerous scientific disciplines. To overcome limitations of current methods, we introduce Surface Patterned Omniphobic Tiles (SPOTs). This platform combines geometry and surface engineering, building on discontinuous wetting approaches to leverage capillarity for metering liquids. The SPOTs platform allows manipulation of hundreds to thousands of independent experiments without expensive equipment or large consumable costs. These devices can handle a wide range of liquid types and volumes (<10 nanoliters to >10 microliters) with better precision than pipetting. The platform is inexpensive and easy to fabricate, fast and intuitive to use, and cross-compatible with existing microwell plate layouts. We demonstrate how these capabilities facilitate diverse experiments including testing antibiotic combinations for synergy and antagonism, material screening of perovskites, and genotyping microbial isolates. We anticipate SPOTs will enable users from disparate domains to quickly and easily run a wide range of high-throughput experiments.

bioengineering↗

Scalable Genotyping of Microbial Colonies

The sequence of the 16S region is taxonomically informative and widely used for genotyping microbes. While it is easy and inexpensive to genotype several isolates by Sanger sequencing the 16S region, this method becomes quite costly if scaled to many isolates. High throughput sequencing provides one potential avenue for obtaining 16S sequences at scale, but presents additional challenges. First, DNA purification workflows for high-throughput sample preparation are labor intensive and expensive. Second, cost-effective multiplexing and library preparation schemes are difficult to implement for many libraries on a single sequencing run. Therefore, we implemented a scalable protocol for isolate genotyping involving colony polymerase chain reaction (PCR) with simple cell lysis as well as a four barcode indexing scheme that enables scalable multiplexing and streamlined library preparation by amplifying with four primers simultaneously in a single reaction. We tested this protocol on 93 colonies cultured from environmental samples, and we were able to ascertain the identity of [~]90% of microbial isolates.

microbiology↗