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. 2018 Dec 13;12(2):346–359. doi: 10.1111/1751-7915.13339

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© 2018 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology.

This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

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Enzyme activity and protein level of PceA_Y51 and DcaA heterologously produced in S. blattae cultivated in the presence of various amendments.

A. The RDase activity was measured in at least two independent cultures. The standard deviation is given. PceA_Y51 was tested for the conversion of PCE, while DcaA was tested with 1,2‐dichloroethane (DCA) as substrate.

B. Immunological detection of both RDases in crude extracts separated on an SDS‐PAGE (25 μg of protein was applied to each lane) with an antibody directed against the Strep‐tag.