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Efficient conversion from polysialogangliosides to monosialotetrahexosylganglioside using Oerskovia xanthineolytica YZ-2
A new sialidase-producing strain isolated from soil was identified as Oerskovia xanthineolytica YZ-2 . Sialidase was produced when Oerskovia xanthineolytica YZ-2 was exposed to polysialogangliosides. The sialidase of Oerskovia xanthineolytica YZ-2 hydrolyzed sialic acid linkages in polysialoganglios...
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Published in: | Bioprocess and biosystems engineering 2011-05, Vol.34 (4), p.493-498 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A new sialidase-producing strain isolated from soil was identified as
Oerskovia xanthineolytica
YZ-2
.
Sialidase was produced when
Oerskovia xanthineolytica
YZ-2 was exposed to polysialogangliosides. The sialidase of
Oerskovia xanthineolytica
YZ-2 hydrolyzed sialic acid linkages in polysialogangliosides, and released monosialotetrahexosylganglioside (GM1). The sialidase had the capability of product specificity because it did not attack the sialic acid linkage in GM1. Therefore,
Oerskovia xanthineolytica
YZ-2 was used for GM1 production from polysialogangliosides. In flasks cultivation phase, it was proved that
Oerskovia xanthineolytica
YZ-2 could convert polysialogangliosides to GM1 efficiently. Scaling-up the bioprocess with 8% crude ganglioside, polysialogangliosides was converted to GM1 by
Oerskovia xanthineolytica
YZ-2 in 30 L bioreactor after 18 h. The relative content of GM1 increased from 16.3% in crude ganglioside to 83.7% after
Oerskovia xanthineolytica
YZ-2 conversion. Therefore, a simple, large-scale conversion process for GM1 production from polysialogangliosides was achieved using O
erskovia xanthineolytica
YZ-2 as a biocatalyst. |
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ISSN: | 1615-7591 1615-7605 |
DOI: | 10.1007/s00449-010-0493-8 |