首页> 美国卫生研究院文献>Applied and Environmental Microbiology >Parvibaculum lavamentivorans DS-1T Degrades Centrally Substituted Congeners of Commercial Linear Alkylbenzenesulfonate to Sulfophenyl Carboxylates and Sulfophenyl Dicarboxylates
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Parvibaculum lavamentivorans DS-1T Degrades Centrally Substituted Congeners of Commercial Linear Alkylbenzenesulfonate to Sulfophenyl Carboxylates and Sulfophenyl Dicarboxylates

机译:Parvibaculum lavamentivorans DS-1T将商业线性烷基苯磺酸盐的集中取代同类物降解为磺基苯基羧酸盐和磺基苯基二羧酸盐

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摘要

Commercial linear alkylbenzenesulfonate (LAS) contains 20 congeners of linear alkanes (C10 to C13) substituted subterminally with the 4-sulfophenyl moiety in any position from lateral to central. Parvibaculum lavamentivorans DS-1T degrades 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 by P. lavamentivorans DS-1 during the degradation of commercial LAS.
机译:商业线性烷基苯磺酸盐(LAS)包含20个同系的直链烷烃(C10至C13),从侧面到中心的任何位置被亚磺酰基部分亚端取代。 Parvibaculum lavamentivorans DS-1 T 降解8个侧向取代的同类物[例如2-(4-磺基苯基)癸烷(2-C10-LAS);在本文中,化合物通过链长(例如,C 10)和取代基在链上的位置(例如,位置2)系统命名为主要的磺基苯基羧酸盐[SPC;这里是3-(4-磺基苯基)丁酸酯(3-C4-SPC)]和两个次要产物,即α,β-不饱和SPC(SPC-2H,这里是3-C4-SPC-2H)和SPC + 2C (此处为5-C6-SPC)物种(D. Schleheck,TP Knepper,K. Fischer,and AM Cook,Appl。Environ.Microbiol。70:4053-4063)。在这项工作中,研究了菌株DS-1对中心取代同源物的降解。 5-C10-LAS不仅产生了预期的4-C8-SPC,4-C8-SPC-2H和6-C10-SPC(约占产品的70%),而且还生成了磺基苯基二羧酸盐(SPdC),即C6-, C8-和C10-SPdC。在通过高压液相色谱法(HPLC)分离后,通过电喷雾电离质谱法(ESI-MS)鉴定它们。使用ESI离子阱质谱仪和ESI飞行时间质谱仪来确认关键中间体的身份。通过HPLC分离商业LAS获得的同类物的不同混合物被降解,并比较了降解产物。如果同类物在5、6或7位带有磺基取代基,则形成SPdC以及SPC,SPC-2H和SPC + 2C,而在2、3或4位上的取代基仅生成SPC, SPC-2H和SPC + 2C。从20个LAS同系物中产生了约50种产物:11个主要SPC,每个具有SPC-2H和SPC + 2C(即33个SPC和SPC-2H物种)和约17个SPdC物种。因此,在商业化LAS降解过程中,P。lavamentivorans DS-1生成了大量化合物,其中很多都是少量的。

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