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Applied and Environmental Microbiology, December 2003, p. 7073-7082, Vol. 69, No. 12
0099-2240/03/$08.00+0 DOI: 10.1128/AEM.69.12.7073-7082.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
Jarno Kallio, and Pirkko Suominen
Roal Oy, FIN-05201 Rajamäki, Finland
Received 30 May 2003/ Accepted 3 September 2003
A
bacterial xylanase gene, Nonomuraea flexuosa xyn11A, was
expressed in the filamentous fungus Trichoderma reesei from
the strong cellobiohydrolase 1 promoter as fusions to a variety of
carrier polypeptides. By using single-copy isogenic transformants, it
was shown that production of this xylanase was clearly increased (up to
820 mg/liter) when it was produced as a fusion protein with a carrier
polypeptide having an intact domain structure compared to the
production (150 to 300 mg/liter) of fusions to the signal sequence
alone or to carriers having incomplete domain structures. The carriers
tested were the T. reesei mannanase I (Man5A, or
MANI) core-hinge and a fragment thereof and the cellulose
binding domain of T. reesei cellobiohydrolase II (Cel6A, or
CBHII) with and without the hinge region(s) and a fragment thereof. The
flexible hinge region was shown to have a positive effect on both the
production of Xyn11A and the efficiency of cleavage of the fusion
polypeptide. The recombinant Xyn11A produced had properties similar to
those of the native xylanase. It constituted 6 to 10% of the
total proteins secreted by the transformants. About three times more of
the Man5A core-hinge carrier polypeptide than of the recombinant Xyn11A
was observed. Even in the best Xyn11A producers, the levels of the
fusion mRNAs were only
10% of the level of
cel7A (cbh1) mRNA in the untransformed host
strain.
Present address: UniCrop Ltd., FIN-00790 Helsinki, Finland.
Present address: Cargill Dow LLC, Minnetonka, MN 55345.
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