Difference between revisions of "Team:TCU Taiwan/Project/Overview"
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− | 2. From <I>Streptomyces lividans</I> to trasport chitinase C to secretion system, which has been proven to work in E.<I>coli</I> | + | 2. From <I>Streptomyces lividans</I> to trasport chitinase C to secretion system, which has been proven to work in E.<I>coli</I> |
by reference. | by reference. | ||
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Revision as of 18:28, 31 August 2015
AMP. coli |
To achieve our goal we incorporated antimicrobial peptides (AMPs) into our medical dressing. AMPs, are stable peptide that have extensive ability in bactericidal effects. Unlike antibiotics, AMPs can puncture the cell membrane to kill the bacteria therefore bypassing bacterial antibiotic drug resistance mechanisms. [1] Besides, the peptides also have ability to help skin recovered. [2]After reading numerous of research articles, we selected two kinds of AMPs: Signiferin and Epinecidin-1 as our reagents. |
• Epinecidin-1: 1. From the skin mucus of Epinephelus coioides a kind of fish. 2. Has function of killing bacteria. 3. In addition, it has the ability to help wounds healing and has been proven by animal studies. • Signiferin: 1. From the skin mucus of Crinia signifera a kind of tree frog. 2. Have function of killing bacteria. 3. Have great ability in disinfect Methicillin-Resistant Staphylococcus aureus (MRSA). 4. Had already been kindly proved by the 2013 TU-Delft iGEM team. 1. Helps AMPs to secret out of E. coli. 2. From Streptomyces lividans to trasport chitinase C to secretion system, which has been proven to work in E.coli by reference. Based on AMPs to develop into a potential material of wound dressing. |
Contact us tcutaiwan@gmail.com No.701, Sec. 3, Zhongyang Rd. Hualien 97004, Taiwan |