A Study of the Effects of Variable Gravitational Environments on Genetic Transformation in E. coli
Overview
Objectives/Goals This scientific experiment sought to measure the effects of microgravity (zero gravity) on bacterial genetic transformation in comparison with those of normal gravity through the use of the pGLO plasmid, which provides for both the increased resistance to antibiotics and the ability to luminesce under ultraviolet light. Methods/Materials Of the plates prepared, one-third were used in a control situation; as such, they were exposed to a constant gravitational environment and hindered from the uptake of the pGLO gene. The remaining two-thirds were introduced to the pGLO gene under variable conditions: one-third was kept in normal gravity (as in the control situation) and the final four plates were placed in the clinostat. Results In addition to a general increase to the amount of colonies present, those in the clinostat exhibited the greatest percentage of transformed colonies. They also expressed the pGLO gene earlier than the plates that were growing at normal gravity. Conclusions/Discussion It can be clearly stated that E. coli grown in a microgravity environment exhibits the greatest adeptness at genetic transformation in that it is able to express the gene at a greater rate efficiency.Combining bacterial replication, genetic recombination, and the use of microgravity conditions may be the key to processing medicines more effectively. The first would ensure quantity (production), the second, efficiency, and the third, speed.
Summary statement
This experiment examined bacterial genetic transformation in simulated microgravity environments in order to find a way to produce organic medicines, such as insulin and interferon, more efficiently.
Help received
School provided lab and most equipment; science teacher provided
Competition history
- CSEF 2007
Resources
Related projects
CSEF · 2007
The Effect of Tc-99 on the Genetic Transformation of E. coli and L. lactis
CSEF · 2006
The Effect of Radiation on the Genetic Transformation of the pGLO Gene in Monera: Phase 2
CSEF · 2009
Optimizing Bacterial Transformation Efficiency: A Study of Heat and Cold Shock Parameters and DNA Plasmid Concentration
CSEF · 2003
The Feasibility of Transforming E. coli Utilizing High Voltage Electroporation
CSEF · 2005
Bacterial Transformations Using the Beta-Galactosidase Gene
CSEF · 2008
War of the Worlds
CSEF · 2017
The Effect of 28 kHz Ultrasound Exposure on the Transformation Efficiency of pGLO Plasmids into E. coli
CSEF · 2010
Modeling Transformed E. coli Growth at Different Ampicillin Concentrations
Closest projects by meaning, across every fair and year in the corpus.
Browse more like this
Source: California Science & Engineering Fair public projects