Low Co2 Screening

Low CO2 screening is a biological testing approach used to identify cells, organisms, or strains that maintain growth or function when carbon dioxide availability is reduced. The method exposes samples to controlled low-CO2 conditions and compares responses such as growth rate, viability, metabolism, photosynthetic performance, or gene expression with those observed under standard conditions. Reduced CO2 can alter dissolved inorganic carbon, intracellular carbon supply, and environmental pH, revealing adaptations that support cellular activity under carbon limitation. In biology and biotechnology, this screening helps characterize stress tolerance, select robust organisms for research or production, and clarify how carbon availability shapes physiology and ecosystem performance.

Low Co2 Screening - Related Videos

Research

JoVE Journal - Biology

High-throughput Screening for Chemical Modulators of Post-transcriptionally Regulated Genes

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2015

Here we describe a cell-based reporter gene assay as a valuable tool to screen chemical libraries for compounds modulating post-transcriptional control mechanisms exerted through 3’ UTR.

Education

JoVE Science Education - Advanced Biology

Genetic Screens

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2023

Genetic screens are critical tools for defining gene function and understanding gene interactions. Screens typically involve mutating genes and then assessing the affected organisms for phenotypes of interest. The process can be “forward”, where mutations are generated randomly to identify unknown genes responsible for the phenotypes, or it can be “reverse”, where specific genes are targeted for mutation to observe what phenotypes are produced.Here, JoVE reviews various types of genetic...

Microscopy-based Assays for High-throughput Screening of Host Factors Involved in Brucella Infection of Hela Cells

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Cited by 6 •

2016

Two assays for microscopy-based high-throughput screening of host factors involved in Brucella infection are described. The entry assay detects host factors required for Brucella entry and the endpoint assay those required for intracellular replication. While applicable for alternative approaches, siRNA screening in HeLa cells is used to illustrate the protocols.

Multi-enzyme Screening Using a High-throughput Genetic Enzyme Screening System

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Cited by 7 •

2016

This work presents a method of high-throughput screening using a universal genetic enzyme screening system that can be theoretically applied to over 200 enzymes. Here, the single screening system identifies three different enzymes (lipase, cellulase, and alkaline phosphatase) by simply changing the substrate used (p-nitrophenyl acetate, p-nitrophenyl-β-D-cellobioside, and phenyl phosphate).

A Robust Method for the Large-Scale Production of Spheroids for High-Content Screening and Analysis Applications

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Cited by 4 •

2021

This protocol details a method for the production of three different types of spheroids in a manner that makes them suitable for large-scale high-content screening and analysis. In addition, examples are presented showing how they can be analyzed at spheroid and individual cell levels.

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