Sir Edward Penley Abraham, (10 June 1913 – 8 May 1999) was an English biochemist instrumental in the development of the first antibiotics penicillin and cephalosporin.
Abraham was born on 10 June 1913 at 47 South View Road, Shirley, Southampton. From 1924 Abraham attended King Edward VI School, Southampton, before achieving a First in Chemistry at The Queen's College, Oxford.
Abraham completed his DPhil at the University of Oxford under the supervision of Sir Robert Robinson, during which he was the first to crystallise lysozyme, an enzyme discovered by Sir Alexander Fleming and shown to have antibacterial properties, and was later the first enzyme to have its structure solved using X-ray crystallography, by Lord David Philips.
Discovery and development of cephalosporins and Penicillin
He then won a Rockefeller Foundation scholarship and spent a year in Stockholm at the Biokemiska Institut.
He then moved back to Oxford and became part of a research team led by Sir Howard Florey at the Sir William Dunn School of Pathology, responsible for the development of penicillin and its medical applications. Sir Edward was specifically involved in the purification process and determination of its chemical structure. In 1940 Edward discovered penicillinase as the cause of bacterial resistance to antibiotics such as penicillin. In October 1943 Abraham and Sir Ernst Boris Chain proposed a novel beta-lactam structure with a fused two ring system. This proposal was confirmed in 1945 by Dorothy Hodgkin using X-ray crystallography. Florey formally recognised Abraham's work in 1948 by nominating him to be one of the first three "penicillin" research Fellows at Lincoln College, Oxford.
Later that year samples of a Cephalosporium acremonium fungus with antibacterial properties were received from Giuseppe Brotzu. Abraham and Guy Newton purified the antibiotics from this fungus and found one, cephalosporin C, was not degraded by penicillinase and hence able to cure infections from penicillin-resistant bacteria.
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Bacteria (bækˈtɪəriə; : bacterium) are ubiquitous, mostly free-living organisms often consisting of one biological cell. They constitute a large domain of prokaryotic microorganisms. Typically a few micrometres in length, bacteria were among the first life forms to appear on Earth, and are present in most of its habitats. Bacteria inhabit soil, water, acidic hot springs, radioactive waste, and the deep biosphere of Earth's crust. Bacteria play a vital role in many stages of the nutrient cycle by recycling nutrients and the fixation of nitrogen from the atmosphere.
An antimicrobial is an agent that kills microorganisms (microbicide) or stops their growth (bacteriostatic agent). Antimicrobial medicines can be grouped according to the microorganisms they act primarily against. For example, antibiotics are used against bacteria, and antifungals are used against fungi. They can also be classified according to their function. The use of antimicrobial medicines to treat infection is known as antimicrobial chemotherapy, while the use of antimicrobial medicines to prevent infection is known as antimicrobial prophylaxis.
The cephalosporins (sg. ˌsɛfələˈspɔːrᵻn,ˌkɛ-,-loʊ-) are a class of β-lactam antibiotics originally derived from the fungus Acremonium, which was previously known as Cephalosporium. Together with cephamycins, they constitute a subgroup of β-lactam antibiotics called cephems. Cephalosporins were discovered in 1945, and first sold in 1964. The aerobic mold which yielded cephalosporin C was found in the sea near a sewage outfall in Su Siccu, by Cagliari harbour in Sardinia, by the Italian pharmacologist Giuseppe Brotzu in July 1945.
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