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--- home:protocol:mp_antibiotics [02.18.2011] – paulalbert
+++ home:protocol:mp_antibiotics [02.23.2011] – paulalbert
@@ Line 36: / Line 36: @@
 |Clindamycin   |interferes with bacterial protein synthesis by binding to the 50S subunit of the bacterial ribosome     |
 |Demeclocycline (Declomycin)  |interferes with bacterial protein synthesis by binding to the 30S and 50S subunit of the bacterial ribosome     |
-|<html>Bactrim DS</html>    |inhibits dihydropteroate synthase, an enzyme that allows bacteria to use folic acid      |
+|Bactrim DS   |inhibits dihydropteroate synthase, an enzyme that allows bacteria to use folic acid      |
 \\
 ==== Inhibition of bacterial ribosome activity (minocycline, azithromycin, clindamycin, demeclocycline) ====
-All the MP antibiotics except Bactrim are bacteriostatic. Bacteriostatic antibiotics are a class of antibiotics that work by disabling bacterial ribosomes – small, dense, structures that allow the pathogens to replicate and survive. When an antibiotics binds to a bacterial ribosome, it limits the growth of bacteria by interfering with bacterial protein production, DNA replication, or other aspects of bacterial cellular metabolism.
+All the MP antibiotics except Bactrim are bacteriostatic. Bacteriostatic antibiotics are a class of antibiotics that work by disabling bacterial ribosomes – small, dense, structures that allow the pathogens to replicate and survive. When an antibiotic binds to a bacterial ribosome, it limits the growth of bacteria by interfering with bacterial protein production, DNA replication, or other aspects of bacterial cellular metabolism.

home/protocol/mp_antibiotics.txt · Last modified: 09.14.2022 by 127.0.0.1