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A miracle antidote in a test tube cannot cure the world if it is too
expensive to produce. Too often the cost of producing sufficient quantities
of a protein for commercial testing is one of the major sticking points
for researchers trying to secure venture capital.
Thats why Dr Michael Cooney from Murdochs School of Engineering
has developed a new pilot scale fed-batch fermenter for researching
DNA protein production.
When moving to production scale fermentation, the pharmaceutical industry
currently sticks with the batch production technique used
in clinical testing. This requires researchers to invest in new and larger
reactors, such as expanding production from a 100L to 500L.
However, according to Dr Cooney, fed-batch processing can
use the smaller reactors without losing the production rate of larger
volumes.
The difference with fed-batch processing is that main
nutrients are fed at a rate that controls the cell growth rate, and hence
the tendency to produce inhibitory by-products. This way, we can obtain
a biomass concentration of a much higher density than in batch
processing, in which all the nutrients are chucked in at the start,
said Dr Cooney.
Working with Dr David Berryman from the State Agricultural Biotechnology
Centre, Dr Cooney has been testing the fed-batch processing reactors
ability to express a particular DNA protein from E. coli since the beginning
of this year.
Dr Cooney, who designed the custom-made reactor, believes that it is
unique in its versatility. The modular based design enables the
reactor to be adapted for other production techniques, he said.
According to Dr Cooney, the most attractive feature of the fermenter
is the computer automation.
Everything from sensors to the rate of inlet gas is carefully
controlled and data logged by the computer. My student, Wayne Johnson,
has also developed a really useful and versatile program to run the reactor.
Its great, added Dr Cooney, because Ive
spent my research career using these terribly limited control systems
provided by fermenter manufacturers. Now we have the flexibility of measurement
and control in a virtual world.
It is Dr Cooneys desire to work with other researchers at Murdoch
who are hoping to eventually market their own proteins.
I hope this system becomes a conduit for Murdochs biomedical
researchers to capitalise on promising results, helping them scale up
the test production of new proteins and collect the type of data necessary
to approach industrial producers.
Murdoch researchers hope to use this technology to optimise production
of a variety of useful proteins, including vaccines and antigens that
can detect particular antibodies.
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Editor Pepi Smyth Writers Lachlan McCrudden, Michael Peeters, Chris Smyth, Pepi Smyth, Marissa Williams Design Peter Roots Photography Grace Banks, Geoff Griffiths, Brian Richards All material may be used without permission but correct reference to persons quoted and the University is requested. Enquiries to The Editor, Synergy (editorcr@central.murdoch.edu.au) Document creation date: 08/02/1999 Expiry date: N/A HTML last modified: 19/12/2001 Modified by: Mark Busani, IT Support Officer Authorised by: Dr Paul D'Sylva, Director, Division of Research & Development Copyright © Murdoch University 2001: Disclaimer and Copyright Notice CRICOS Provider Code: 00125J |
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