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两亲性三阳离子卟啉和5,10,15,20-四(4-N,N,N-三甲基铵苯基)卟啉对大肠杆菌进行光动力灭活的机制

Mechanisms of Escherichia coli photodynamic inactivation by an amphiphilic tricationic porphyrin and 5,10,15,20-tetra(4-N,N,N-trimethylammoniumphenyl) porphyrin.

作者信息

Caminos Daniel A, Spesia Mariana B, Pons Patricia, Durantini Edgardo N

机构信息

Departamento de Química, Universidad Nacional de Río Cuarto, Río Cuarto, Agencia Postal Nro. 3, X5804BYA, Río Cuarto, Córdoba, Argentina.

出版信息

Photochem Photobiol Sci. 2008 Sep;7(9):1071-8. doi: 10.1039/b804965c. Epub 2008 Jul 28.

Abstract

The mechanistic aspects of Escherichia coli photodynamic inactivation (PDI) have been investigated in bacteria treated with 5,10,15-tris[4-(3-N,N,N-trimethylammoniumpropoxy)phenyl]-20-(4-trifluoromethylphenyl)porphyrin iodide (A3B3+) and visible light. The photosensitization activity of A3B3+ porphyrin was compared with that of 5,10,15,20-tetra(4-N,N,N-trimethylammonium phenyl)porphyrin p-tosylate (TMAP4+), which is an active tetracationic sensitizer to eradicate bacteria. The PDI damages on plasmid and genomic DNA were analyzed by electrophoresis. DNA photocleavage was observed after a long period of irradiation, when the bacterial cells are largely photoinactivated. Transmission electron microscopy (TEM) revealed structural changes with appearance of low density areas into the cells and irregularities in cell barriers, which could affect the normal cell membrane functionality. Also, damages on the cell-wall were not detected by scanning electron microscopy (SEM) and release of intracellular biopolymers was not found after PDI. These results indicate that the photodynamic activity of these cationic porphyrins produces DNA photodamage after a long period of irradiation. Therefore, an interference with membrane functions could be the main cause of E. coli photoinactivation upon short PDI treatments.

摘要

已在用碘化5,10,15 - 三[4 - (3 - N,N,N - 三甲基铵丙氧基)苯基]-20 - (4 - 三氟甲基苯基)卟啉(A3B3+)和可见光处理的细菌中研究了大肠杆菌光动力失活(PDI)的机制。将A3B3+卟啉的光敏活性与5,10,15,20 - 四(4 - N,N,N - 三甲基铵苯基)卟啉对甲苯磺酸盐(TMAP4+)进行了比较,TMAP4+是一种用于根除细菌的活性四价阳离子敏化剂。通过电泳分析了PDI对质粒和基因组DNA的损伤。在长时间照射后,当细菌细胞基本被光灭活时,观察到了DNA光裂解。透射电子显微镜(TEM)显示细胞内出现低密度区域以及细胞屏障不规则,这可能会影响正常细胞膜功能。此外,扫描电子显微镜(SEM)未检测到细胞壁损伤,PDI后也未发现细胞内生物聚合物释放。这些结果表明,这些阳离子卟啉的光动力活性在长时间照射后会产生DNA光损伤。因此短时间PDI处理后,对膜功能的干扰可能是大肠杆菌光失活的主要原因。

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