کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2807 136 2016 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Correlation among phenyltins molecular properties, degradation and cellular influences on Bacillus thuringiensis in the presence of biosurfactant
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی بیو مهندسی (مهندسی زیستی)
پیش نمایش صفحه اول مقاله
Correlation among phenyltins molecular properties, degradation and cellular influences on Bacillus thuringiensis in the presence of biosurfactant
چکیده انگلیسی


• SFAE altered peptide structure of cell wall accelerating TPT binding and transport.
• SFAE enhanced TPT solubility and degradation.
• TPT degradation pathway was determined by bond energy of SnC bonds.
• TPT is successively degraded to form DPT and MPT, and finally to tin.
• SFAE enhanced ATPase activities, cell metabolism, PO43–, Na+ and carbon use.

Although a successive dearylation is recognized as a triphenyltin biodegradation pathway, the cleavage pattern of the various chemical bonds of phenyltins is still not clear. Moreover, the correlation among phenyltins biosorption, degradation, molecular properties and metabolic impacts is far from fully understood. Therefore, phenyltins treatment of Bacillus thuringiensis was conducted. After degradation for 7 d in the presence of 50 mg L−1 of the surfactant sucrose fatty acid ester, the degradation efficiency of 1 mg L−1 triphenyltin reached its peak value of 89%. The surfactant altered the topological structure of the cellular peptide chains, accelerated triphenyltin binding and transport, increased cellular viability, Na+/K+- and Ca2+/Mg2+-ATPase activities, increased PO43–and Na+ assimilation, and decreased K+ and Mg2+ release, resulting in the enhancement of triphenyltin degradation. However, surfactant did not change the successive dephenylation pathway, which was primarily determined by the bond energy of each SnC bond of triphenyltin

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ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochemical Engineering Journal - Volume 105, Part A, 15 January 2016, Pages 71–79
نویسندگان
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