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Biology subjects

Seder, I.

Publications and source records attributed to Seder, I..

2 recordsLinked to original sources

Fast and sensitive multiplexed diagnostic system enabled by real-time solid-phase PCR assay

Simultaneous identification of multiple nucleic acid targets is pivotal for high-throughput analysis in clinical diagnostics. Unfortunately, conventional PCR offers limited multiplexing capability due to issues like primer interference, fluorescence spectral overlaps and instrumentation complexity. Solid-phase PCR (SP-PCR), in which primers are physically separated on a solid support, has emerged as an alternative strategy for detection of multiple targets in parallel. However, SP-PCR has been suffering from low efficiency, long reaction time, inability for real-time signal monitoring and accurate quantification, which greatly restricts their applications in multiplexed assays. In this study, we presented for the first time a compact and portable flow-through SP-PCR platform to permit rapid, highly efficient and quantitative solid-phase amplification. We designed an integrated platform comprising a novel mechanically actuated valving system and a dual-chamber SP-PCR system to enable automated sample purification and amplification. Active oscillating the PCR solution between the chambers significantly enhanced the mass diffusion over the solid-phase array. Moreover, after each amplification cycle, the PCR solution was separated from the solid-phase-bound probes, thereby eliminating background signal interference and allowing for real-time monitoring of SP-PCR signals without the need for complex optical systems. The flow-through SP-PCR system demonstrated quantitative detection of five viral pathogens in a single reaction, with a limit of detection of 10 copies per reaction within 20 minutes. This platform provides a promising high-throughput, low-cost and simple-instrumentation multiplexed diagnostic system.

molecular biology↗

Metabolic Engineering on a 3D-Printed Microfluidic Platform: A New Approach for Modular Co-Metabolic pathways

Metabolic engineering of cell factories often requires extensive modification of host cellular machinery, leading to numerous challenges such as metabolic burden, intermediate metabolite toxicity, and inadequate endogenous fluxes. To overcome the limitations, we presented an innovative approach for metabolic engineering, by constructing modular biosynthetic pathways on a 3D-printed microfluidic platform. Several new techniques have been developed, including novel designs of chip configurations, effective methods for enzyme immobilization on printed resins, and proper ways to regenerate cofactors in redox reactions. As a proof of concept, we built xylose consumption and CO2 fixation pathways in the microfluidic chips and successfully demonstrated that the platform was able to convert xylose and enable the rapid growth of Saccharomyces cerevisiae, which otherwise will not grow with xylose as the only carbon source. Overall, the 3D-printed microfluidic platform presents a much simpler and more efficient cell-free strategy for developing modular, optimized biosynthetic pathways.

bioengineering↗