Cycloheximide
Cycloheximide is a fungicide and antibiotic that inhibits protein synthesis in eukaryotic cells. It is produced by the bacterium Streptomyces griseus. Cycloheximide exerts its effect by interfering with the translocation step in protein synthesis, thus blocking the elongation of the protein chain on ribosomes. Due to its mode of action, cycloheximide is widely used in molecular biology and biochemistry for research purposes, particularly in studies involving the control of protein synthesis and cell death mechanisms.
Mechanism of Action[edit | edit source]
Cycloheximide binds to the Eukaryotic 80S ribosome, specifically to the 60S subunit, and inhibits the translocation step of protein synthesis. This inhibition prevents the movement of mRNA and tRNA from the A site to the P site within the ribosome, effectively halting the elongation of the nascent protein chain. This action is highly specific to eukaryotic cells, making cycloheximide a useful tool for distinguishing between eukaryotic and prokaryotic protein synthesis in experimental settings.
Applications in Research[edit | edit source]
Cycloheximide is extensively used in the field of molecular biology and genetics for its ability to inhibit protein synthesis in eukaryotic cells. It is particularly valuable in studies of gene expression, apoptosis (programmed cell death), and the effects of protein synthesis inhibition on cell growth and survival. Additionally, cycloheximide is used in selective media for the isolation of certain bacteria that are resistant to its effects, thereby serving as a tool for bacterial identification and study.
Toxicity and Safety[edit | edit source]
While cycloheximide is a powerful tool for research, it is also highly toxic to humans and animals if ingested, inhaled, or absorbed through the skin. It can cause a range of adverse health effects, including allergic reactions, skin irritation, and potentially severe damage to internal organs. Due to its high toxicity, the use of cycloheximide in the laboratory requires strict safety precautions, including the use of personal protective equipment (PPE) and proper ventilation.
Regulatory Status[edit | edit source]
Due to its toxicity, the use of cycloheximide is regulated in many countries. It is primarily used for research purposes and is not approved for use in agriculture or as a therapeutic agent in humans or animals. Regulatory agencies may require special permits for the purchase, storage, and disposal of cycloheximide to ensure it is used safely and responsibly.
Conclusion[edit | edit source]
Cycloheximide remains an important tool in molecular biology and biochemistry for the study of protein synthesis and cell biology. Despite its utility, the compound's toxicity necessitates careful handling and adherence to safety protocols. Ongoing research into the mechanisms of action and applications of cycloheximide continues to contribute to our understanding of cellular processes and the development of new scientific methodologies.
Cycloheximide Resources | |
---|---|
|
Search WikiMD
Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD
WikiMD's Wellness Encyclopedia |
Let Food Be Thy Medicine Medicine Thy Food - Hippocrates |
Translate this page: - East Asian
中文,
日本,
한국어,
South Asian
हिन्दी,
தமிழ்,
తెలుగు,
Urdu,
ಕನ್ನಡ,
Southeast Asian
Indonesian,
Vietnamese,
Thai,
မြန်မာဘာသာ,
বাংলা
European
español,
Deutsch,
français,
Greek,
português do Brasil,
polski,
română,
русский,
Nederlands,
norsk,
svenska,
suomi,
Italian
Middle Eastern & African
عربى,
Turkish,
Persian,
Hebrew,
Afrikaans,
isiZulu,
Kiswahili,
Other
Bulgarian,
Hungarian,
Czech,
Swedish,
മലയാളം,
मराठी,
ਪੰਜਾਬੀ,
ગુજરાતી,
Portuguese,
Ukrainian
WikiMD is not a substitute for professional medical advice. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.
Contributors: Prab R. Tumpati, MD