Tetracycline
Presented by :- Khushbu Kumari
Roll no. :- 201631
Department of Biotechnology
Central University of Haryana
General introduction
What is Tetracycline ?
Tetracycline is an antibiotic that fights against infection caused by
bacteria.
Belongs to a family of broad spectrum antibiotics effective against
remarkably wide variety of organisms.
Tetracycline is used to treat many different bacterial infections of the
skin, intestines, respiratory tract, urinary tract, genitals, lymph nodes,
and other body systems. It is often used in treating severe acne, or
sexually transmitted diseases such as syphilis, gonorrhea.
Isolated directly from several species of Streptomyces bacteria or
produced semi-synthetically from those isolated compounds.
History
Chlortetracycline (trade name Aureomycin, Lederle Laboratories) is a tetracycline
antibiotic, the first tetracycline to be identified. It was discovered in 1945 at Lederle
Laboratories under the supervision of scientist Yellapragada Subbarow and
Benjamin Minge Duggar. Duggar identified the antibiotic as the product of an
actinomycete he cultured from a soil sample collected from Sanborn Field at the
University of Missouri.The organism was named Streptomyces aureofaciens and the
isolated drug, Aureomycin, because of their golden color.
Chlortetracycline
Classification of tetracycline
● On the basis of sources:
● On the basis of duration of action:
(i) Short acting tetracyclines(half life 6-8 hrs): Chlortetracycline,
oxytetracycline and tetracycline.
(ii) Intermediate acting tetracyclines (half life 12 hrs):
Demeclocycline and methacycline.
(iii) Long acting tetracyclines(half life 16 hrs): Doxycycline and
minocycline.
Naturally occuring
● Tetracycline
● Chlortetracycline
● Oxytetracycline
● Demeclocycline
Semi synthetic
● Doxycycline
● Meclocycline
● Methacycline
● Minocycline
Structure Activity Relationship
Mechanism of action
● They are short-acting and passively
diffuse through porin channels in the
bacterial membrane.
● They inhibit protein synthesis by
binding reversibly to the bacterial 30S
ribosomal subunit and preventing the
aminoacyl tRNA from binding to the A
site of the ribosome.
● They also bind to some extent the
bacterial 50S ribosomal subunit and
may alter the cytoplasmic membrane
causing intracellular components to
leak from bacterial cells.
Mechanism of Resistance
Pharmacokinetics
Tetracyclines can be divided into three main groups based on
Pharmacokinetics
Synthesis
Applications
Adverse effects
● Teeth and bones damage
● Cause skin reaction
● Nail fluorescence
References
https://www.slideshare.net/DrMitalThamke/tetracycline-and-its-mo
difications-pptx-seminar-5
https://biomedres.us/fulltexts/BJSTR.MS.ID.001475.php
https://patents.google.com/patent/US3429781A/en

PPT on Tetracycline antibiotic (2).pdf