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BioMed Central Page 1 of 1 (page number not for citation purposes) Microbial Cell Factories Open Access Poster Presentation Native and heterologous protein oxidation and subsequent degradation in a recombinant filamentous fungus Aspergillus niger B1-D Qiang Li*, Linda M Harvey and Brian McNeil Address: Strathclyde Fermentation Centre, Department of Bioscience, University of Strathclyde, 204 George Street, Glasgow G1 1XW, UK * Corresponding author Filamentous fungi have attracted extensive research inter- est due to their abilities to secrete large amounts of high- valued recombinant proteins. Despite the fact that pro- teases have been recognized as one of the main problems in protein production, little is known about the regulation of them. In the present study, we hypothesized that reac- tive oxygen species (ROS), unavoidable by-products in all aerobic cultures, may cause protein oxidation and induce proteolysis in filamentous fungi. To test this hypothesis, we used a variety of oxidative stressors, oxygenation, menadione, hydrogen peroxide, hydrogen peroxide with copper ion, to study the induction of intracellular proteo- lytic activities in A. niger B1-D, a recombinant filamentous fungus secreting hen egg white lysozyme. Protein carbo- nyl content was monitored as a bio-marker for protein oxidation. Our results show that oxygenation and metal- catalyzed oxidation significantly induce carbonyl groups to bovine serum albumin (BSA). We also found that pro- teolytic activities and carbonyl content increase on the addition of these stressors to the whole broth in A. niger B1-D, and the responses are dose-dependent. In conclu- sion, ROS overproduction correlates with protein oxida- tion and proteolysis in A. niger B1-D. It is advisable to decrease ROS production in the bioprocess of filamentous fungi in order to achieve a higher productivity of heterol- ogous proteins. from The 4th Recombinant Protein Production Meeting: a comparative view on host physiology Barcelona, Spain. 21–23 September 2006 Published: 10 October 2006 Microbial Cell Factories 2006, 5(Suppl 1):P6 doi:10.1186/1475-2859-5-S1-P6 <supplement> <title> <p>The 4th Recombinant Protein Production Meeting: a comparative view on host physiology</p> </title> <sponsor> <note>The organisers would like to thank Novozymes Delta Ltd who generously supported the meeting.</note> </sponsor> <note>Meeting abstracts – A single PDF containing all abstracts in this supplement is available <a href="http://www.biomedcentral.com/content/files/pdf/1475-2859-5-S1-full.pdf">here</a>.</note> <url>http://www.biomedcentral.com/content/pdf/1475-2859-5-S1-info.pdf</url> </supplement> © 2006 Li et al; licensee BioMed Central Ltd.

Native and heterologous protein oxidation and subsequent degradation in a recombinant filamentous fungus Aspergillus niger B1-D

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Microbial Cell Factories

Open AccessPoster PresentationNative and heterologous protein oxidation and subsequent degradation in a recombinant filamentous fungus Aspergillus niger B1-DQiang Li*, Linda M Harvey and Brian McNeil

Address: Strathclyde Fermentation Centre, Department of Bioscience, University of Strathclyde, 204 George Street, Glasgow G1 1XW, UK

* Corresponding author

Filamentous fungi have attracted extensive research inter-est due to their abilities to secrete large amounts of high-valued recombinant proteins. Despite the fact that pro-teases have been recognized as one of the main problemsin protein production, little is known about the regulationof them. In the present study, we hypothesized that reac-tive oxygen species (ROS), unavoidable by-products in allaerobic cultures, may cause protein oxidation and induceproteolysis in filamentous fungi. To test this hypothesis,we used a variety of oxidative stressors, oxygenation,menadione, hydrogen peroxide, hydrogen peroxide withcopper ion, to study the induction of intracellular proteo-lytic activities in A. niger B1-D, a recombinant filamentousfungus secreting hen egg white lysozyme. Protein carbo-nyl content was monitored as a bio-marker for proteinoxidation. Our results show that oxygenation and metal-catalyzed oxidation significantly induce carbonyl groupsto bovine serum albumin (BSA). We also found that pro-teolytic activities and carbonyl content increase on theaddition of these stressors to the whole broth in A. nigerB1-D, and the responses are dose-dependent. In conclu-sion, ROS overproduction correlates with protein oxida-tion and proteolysis in A. niger B1-D. It is advisable todecrease ROS production in the bioprocess of filamentousfungi in order to achieve a higher productivity of heterol-ogous proteins.

from The 4th Recombinant Protein Production Meeting: a comparative view on host physiologyBarcelona, Spain. 21–23 September 2006

Published: 10 October 2006

Microbial Cell Factories 2006, 5(Suppl 1):P6 doi:10.1186/1475-2859-5-S1-P6

<supplement> <title> <p>The 4th Recombinant Protein Production Meeting: a comparative view on host physiology</p> </title> <sponsor> <note>The organisers would like to thank Novozymes Delta Ltd who generously supported the meeting.</note> </sponsor> <note>Meeting abstracts – A single PDF containing all abstracts in this supplement is available <a href="http://www.biomedcentral.com/content/files/pdf/1475-2859-5-S1-full.pdf">here</a>.</note> <url>http://www.biomedcentral.com/content/pdf/1475-2859-5-S1-info.pdf</url> </supplement>

© 2006 Li et al; licensee BioMed Central Ltd.