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INCREASED PRODUCTION
Scientists were also determined to find another strain of Penicillium that might grow better in the huge deep fermentation tanks. Army pilots sent back soil samples from all over the world to be tested for molds. Residents of Peoria, Illinois, were encouraged to bring moldy household objects to the local U.S. Department of Agriculture laboratory, where penicillin research was being conducted. Laboratory staff members also kept an eye out for promising molds while grocery shopping or cleaning out their refrigerators.
In 1943, laboratory worker Mary Hunt brought in an ordinary supermarket cantaloupe infected with a mold that had "a pretty, golden look." This Penicillium species, Penicillium chrysogenum grew so well in a tank that it more than doubled the amount of penicillin produced. The deep fermentation method, the use of corn steep liquor and the discovery of P. chrysogenumby Mary Hunt made the commercial production of penicillin possible. Researchers continued to find higher-yielding Penicillium molds, and also produced higher yielding strains by exposing molds to x-rays or ultraviolet light.
INTRODUCTION
Penicillin is one of the earliest discovered and widely used antibiotic agents, derived from the Penicillium mold. Antibiotics are natural substances that are released by bacteria and fungi into their environment, as a means of inhibiting other organisms - it is chemical warfare on a microscopic scale.
What is Penicillium?
Penicillium is a member of the deuteromycetes, fungi with no known sexual state. Some species of Penicillium have an additional sexual state in the Ascomycota in the Eurotiales.
Species
Penicillium, commonly known as "bread mold", is a genus of fungus that includes:
Penicillium notatum (chrysogenum), which produces the penicillin antibiotic.
Penicillium glaucum, which is used in making Gorgonzola cheese.
Penicillium candida, which is used in making Brie and Camembert cheese, also see Candida.
Penicillium roqueforti, which is used in making Roquefort and Danish Blue cheese.
Penicillium marneffei, a thermally dimorphic species endemic in Southeast Asia, which presents a threat of systemic infection to AIDS patients.
Penicillium bilaiae, which is an agricultural inoculant.
Penicillium camemberti, is used in the production of Camembert and Brie cheeses.
Penicillium spp.
Penicillium marneffei yeast phase 35°C, GMS showing the intracellular yeast-like organism
Penicillium marneffei at 25°C
Species of Penicillium are recognized by their dense brush-like spore-bearing structures. The conidiophores are simple or branched and are terminated by clusters of flask-shaped phialides. The spores (conidia) are produced in dry chains from the tips of the phialides, with the youngest spore at the base of the chain, and are nearly always green. Branching is an important feature for identifying Penicillium species. Some are unbranched and simply bear a cluster of phialides at the top of the stipe. Others may have a cluster of branches, each bearing a cluster of phialides. A third type has branches bearing a second order of branches, bearing in turn a cluster of phialides. These three types of spore bearing systems (penicilli) are called monoverticillate, biverticillate and terverticillate respectively.
CREDITS
http://www.doctorfungus.org/thefungi/Penicillium.htmhttp://en.wikipedia.org/wiki/Penicillium
PRODUCTION IN THE PAST
It took over 5 years to turn the Penicillium notatum mould into the penicillin we know today. It was a long, tedious often frustrating task requiring the brilliant minds of many scientists led by Howard Florey.
The production of penicillin by Florey's team was undertaken in stages:
Stage 1. Growing the Mould
Howard Florey and Ernest Chain began to investigate Alexander Fleming’s Penicillium notatum mould. They knew the mould produced an antibacterial substance and wanted to find out more about it. The mould grew slowly and had very special needs. The scientists began to grow it in different media containing marmite, malt extract, meat and yeast extracts. They studied the rate of growth of the mould and thought about what effect it would have on different bacteria. This work on the rate of growth continued while all the other experiments were taking place, so they could continue to increase the production of penicillin.
Stage 2. Testing
Florey, Chain and the team began to take the juice from under the mould and test it on bacteria. Norman Heatley designed and made a special dish so they could easily test how mould affected different bacteria. They became convinced that penicillin could kill harmful bacteria. How to extract and purify the penicillin from the brown juice was their next challenge.
Stage 3 Extraction
The penicillin was very unstable and short-lived. The scientists worked hard to find a better way of extracting it. At first, the mould juice was simply filtered through parachute silk. Chain found a way to extract the penicillin from the mould juice by passing it through different solvents. He worked out a way to put the mould juice through a series of chemical steps. Each step isolated, purified and concentrated the penicillin in the liquid. This worked, however not as well as they would have liked. At this stage Heatley devised a clever trick called the solvent transfer process.
" Heatley’s method of reversing the chemical path which Chain had followed and of extracting the penicillin from the mould juice into ether and then passing it back through a chemically neutral buffer material produced a superior extract..." [ Source: Bickel ]
This meant that they were able to obtain more penicillin from the mould. They managed to obtain 100 grams of brown powder containing penicillin which could be used to conduct further experiments.
The first extraction plant consisted of inverted bottles with separating funnels and to minimise destruction of the penicillin during water to solvent extractions they needed to do it in cool conditions. They used a cramped store room or the roof of the laboratory. This was very uncomfortable work especially in the middle of winter. The second extraction plant was developed a year later.
Stage 4 Experimentation
Florey's team began to experiment with this brown powder containing penicillin, to see what effect it had on other organisms . Chain dissolved it in water and injected it into two mice. The mice showed no ill effects from the injected powder. That was amazing as the powder was almost 99% impure. At this time, Chain thought it was all penicillin, however any one of the impurities could have killed the mice. The outcome was one of the many strokes of good luck to go the team’s way. The team now began to experiment with the powder to see if it was toxic. They increased the strength and tested it on blood, hormones, cells, etc.
Stage 5 The Mice Experiment
One morning Florey injected a lethal dose of bacteria Streptococcus pyogenes into 8 mice. Four infected mice were given injections of penicillin. Florey and his laboratory assistant James Kent watched the mice carefully. Later that night Heatley arrived and continued to keep watch over the mice. By 3.30 am the 4 mice that did not receive any penicillin were all dead. The bacteria had killed them. All the mice that had received the penicillin were healthy. This proved that penicillin killed deadly bacteria without harming animals. Florey said 'It looks like a miracle".
Stage 6 Increased Production
Now the race was on to make enough penicillin to begin testing it on humans. They needed to grow a lot of mould so they used any container they could find. A flat container was ideal so the mould could grow over a large surface and they could drain the mould juice from under it. They tried biscuit tins, trays, dishes, pans and lids, however bed pans were the best. Thus they designed and made special pottery flasks shaped like bed pans. Heatley made a trolley that held six flasks that could be tipped so the mould juice could be drained off without killing the mould.
During this time the scientists had problems with contamination and at times the penicillin yield from batches of mould was virtually nothing. They continued to work to solve these problems.
The second extraction plant was made almost entirely from junk. It included a bath, milk cans, a milk cooler, a letter box, aquarium pumps and various taps and valves. The mould was grown in culture vessels, filtered then cooled and passed through the solvents to extract the penicillin and purify it. The solvents were separated and the penicillin freeze dried.
Stage 7 Human Testing
The testing to see if penicillin was toxic to humans continued for a long time. It was not until February 1941 that they were ready to inject penicillin into a person who had an infection. Albert Alexander was chosen to receive the first dose of penicillin. He was a police officer whose body was so badly infected he was near death. He was given penicillin by intravenous drip and within 24 hours he was showing remarkable signs of recovery. In 4 days he appeared to be a lot better, however it was at this time the penicillin ran out. They even filtered his urine to retrieve any penicillin so they could continue the treatment, however Albert Alexander died. Florey was determined not to test penicillin on another adult until they had enough to completely cure the patient.
Stage 8 The American Connection
Britain was at war with Germany, therefore money for research was difficult to obtain. Florey and Heatley traveled to the United States of America to get assistance with increasing the production of penicillin, so they could test it properly on humans. They received assistance and it was in America they found corn steep liquor , that proved to be a better food source for growing the mould. It was still very difficult to grow and manufacture and a search went out for people to bring in any Penicillium notatum they found to see if they could find a better strain of mould. A woman they nicknamed ‘Mouldy Mary’ found a mouldy melon that had a mould on it called Penicillium chrysogenum. This turned out to be a better mould strain as it produced higher yields of penicillin.
Heatley stayed in America and with other scientists, worked on growing the mould deep inside tanks filled with nutrient. This increased the production of penicillin but they still did not make enough to begin human trials.
Stage 9 Back in England
In England, Florey’s team continued to use their extraction plant to produce penicillin. Ernest Chain continued to refine the extraction and purification of the penicillin. In 1943, the British Government gave Florey and the team all the resources they needed. The Sir William Dunn School was turned into a penicillin production factory. A team of women were trained as mould farmers. They cared for hundreds of jars of mould. Increased means of extraction and purification meant there was enough penicillin to treat wounded soldiers. It was an outstanding success and 95% of war wounds treated with penicillin healed.
Work continued on refining the production process and by 1945 enough penicillin was being produced world wide to treat patients with bacterial infections.