Parvibaculum lavamentivoransDS-1TDegrades Centrally Substituted Congeners of Commercial Linear Alkylbenzenesulfonate to Sulfophenyl Carboxylates and Sulfophenyl Dicarboxylates

Author:

Schleheck David12,Knepper Thomas P.3,Eichhorn Peter4,Cook Alasdair M.1

Affiliation:

1. Department of Biology, The University of Konstanz, D-78457 Konstanz, Germany

2. School of Biotechnology and Biomolecular Sciences and Centre for Marine Biofouling and BioInnovation, University of New South Wales, Sydney, NSW 2052, Australia

3. Europa Institute of Applied Sciences Fresenius, D-65510 Idstein, Germany

4. State University of New York at Buffalo, Buffalo, New York 14260

Abstract

ABSTRACTCommercial linear alkylbenzenesulfonate (LAS) contains 20 congeners of linear alkanes (C10to C13) substituted subterminally with the 4-sulfophenyl moiety in any position from lateral to central.Parvibaculum lavamentivoransDS-1Tdegrades each of eight laterally substituted congeners [e.g., 2-(4-sulfophenyl)decane (2-C10-LAS); herein, compounds are named systematically by chain length (e.g., C10) and by the position of the substituent on the chain (e.g., position 2)] to a major sulfophenyl carboxylate [SPC; here 3-(4-sulfophenyl)butyrate (3-C4-SPC)] and two minor products, namely, the α,β-unsaturated SPC (SPC-2H, here 3-C4-SPC-2H) and the SPC+2C (here 5-C6-SPC) species (D. Schleheck, T. P. Knepper, K. Fischer, and A. M. Cook, Appl. Environ. Microbiol. 70:4053-4063). The degradation of centrally substituted congeners by strain DS-1 was examined in this work. 5-C10-LAS yielded not only the predicted 4-C8-SPC, 4-C8-SPC-2H, and 6-C10-SPC (about 70% of products) but also sulfophenyl dicarboxylates (SPdC), i.e., C6-, C8-, and C10-SPdC. These were identified by electrospray ionization-mass spectrometry (ESI-MS) after separation by high-pressure liquid chromatography (HPLC). ESI ion-trap MS and ESI-time of flight-MS were used to confirm the identities of key intermediates. Different mixtures of congeners obtained by separation of commercial LAS by HPLC were degraded, and the degradative products were compared. If a congener carried the sulfophenyl substituent on the 5, 6, or 7 position, SPdCs were formed as well as SPC, SPC-2H, and SPC+2C, whereas the substituent on the 2, 3, or 4 position yielded only SPC, SPC-2H, and SPC+2C. Some 50 products were generated from the 20 LAS congeners: 11 major SPCs, each with an SPC-2H and an SPC+2C (i.e., 33 SPC and SPC-2H species), and about 17 SPdC species. A large array of compounds, many in low quantities, is thus generated byP. lavamentivoransDS-1 during the degradation of commercial LAS.

Publisher

American Society for Microbiology

Subject

Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology

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