Abstrakti
The first enzyme in the microcystin (MC) degradation pathway identified in bacterial strains is coded by . mlrA gene and is referred to as microcystinase. To date, there has been no biochemical characterisation of this enzyme. The results presented herein show a successful heterologous expression of MlrA as well as mutational studies, partial purification and biochemical characterisation of the enzyme. The mutation and inhibition study confirmed previous ideas that MlrA is a metalloprotease and allowed to calculate the inhibition parameters. Moreover, the kinetic parameters of MC-LR linearization were measured showing that MlrA exhibits a positive cooperativity towards MC-LR. Furthermore, . in vitro experiments with . Escherichia coli cells expressing MlrA indicated the potency of the heterologous host to eliminate MCs with very high efficiency. This study reports a new approach to the analysis of a microcystin degrading enzyme, extends the knowledge about MC biodegradation and opens broad scope for future study.
| Alkuperäiskieli | Englanti |
|---|---|
| Sivut | 578-586 |
| Sivumäärä | 9 |
| Julkaisu | Toxicon |
| Vuosikerta | 59 |
| Numero | 5 |
| DOI - pysyväislinkit | |
| Tila | Julkaistu - huhtik. 2012 |
| OKM-julkaisutyyppi | A1 Julkaistu artikkeli, soviteltu |
Rahoitus
This research was supported by MNiSW , Poland (grant No 4360/B/P01/2010/39) and by UJ , Poland (grant WRBW BW/47 and BW/147).
Sormenjälki
Sukella tutkimusaiheisiin 'Heterologous expression and characterisation of microcystinase'. Ne muodostavat yhdessä ainutlaatuisen sormenjäljen.Viittausmuodot
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