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BMC Microbiol. 2016 May 23;16:92. doi: 10.1186/s12866-016-0703-x.

Biochemical and spectroscopic characterization of purified Latex Clearing Protein (Lcp) from newly isolated rubber degrading Rhodococcus rhodochrous strain RPK1 reveals novel properties of Lcp.

Author information

1
Institute of Microbiology, University of Stuttgart, Allmandring 31, 70569, Stuttgart, Germany.
2
Prince of Songkla University, Songkla, Thailand.
3
Institute of Microbiology, University of Stuttgart, Allmandring 31, 70569, Stuttgart, Germany. dieter.jendrossek@imb.uni-stuttgart.de.

Abstract

BACKGROUND:

Biodegradation of rubber (polyisoprene) is initiated by oxidative cleavage of the polyisoprene backbone and is performed either by an extracellular rubber oxygenase (RoxA) from Gram-negative rubber degrading bacteria or by a latex clearing protein (Lcp) secreted by Gram-positive rubber degrading bacteria. Only little is known on the biochemistry of polyisoprene cleavage by Lcp and on the types and functions of the involved cofactors.

RESULTS:

A rubber-degrading bacterium was isolated from the effluent of a rubber-processing factory and was taxonomically identified as a Rhodococcus rhodochrous species. A gene of R. rhodochrous RPK1 that coded for a polyisoprene-cleaving latex clearing protein (lcp Rr ) was identified, cloned, expressed in Escherichia coli and purified. Purified LcpRr had a specific activity of 3.1 U/mg at 30 °C and degraded poly(1,4-cis-isoprene) to a mixture of oligoisoprene molecules with terminal keto and aldehyde groups. The pH optimum of LcpRr was higher (pH 8) than for other rubber-cleaving enzymes (≈ pH 7). UVvis spectroscopic analysis of LcpRr revealed a cytochrome-specific absorption spectrum with an additional feature at long wavelengths that has not been observed for any other rubber-cleaving enzyme. The presence of one b-type haem in LcpRr as a co-factor was confirmed by (i) metal analysis, (ii) solvent extraction, (iii) bipyridyl assay and (iv) detection of haem-b specific m/z values via mass-spectrometry.

CONCLUSIONS:

Our data point to substantial differences in the active sites of Lcp proteins obtained from different rubber degrading bacteria.

KEYWORDS:

Biodegradation; Dioxygenase; Latex clearing protein (Lcp); Rhodococcus; Rubber oxygenase

PMID:
27215318
PMCID:
PMC4877957
DOI:
10.1186/s12866-016-0703-x
[Indexed for MEDLINE]
Free PMC Article

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