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异养细菌产生细胞外超氧阴离子的广泛现象。

Widespread production of extracellular superoxide by heterotrophic bacteria.

机构信息

School of Engineering and Applied Sciences, Harvard University, Cambridge, MA 02138, USA.

出版信息

Science. 2013 Jun 7;340(6137):1223-6. doi: 10.1126/science.1237331. Epub 2013 May 2.

Abstract

Superoxide and other reactive oxygen species (ROS) originate from several natural sources and profoundly influence numerous elemental cycles, including carbon and trace metals. In the deep ocean, the permanent absence of light precludes currently known ROS sources, yet ROS production mysteriously occurs. Here, we show that taxonomically and ecologically diverse heterotrophic bacteria from aquatic and terrestrial environments are a vast, unrecognized, and light-independent source of superoxide, and perhaps other ROS derived from superoxide. Superoxide production by a model bacterium within the ubiquitous Roseobacter clade involves an extracellular oxidoreductase that is stimulated by the reduced form of nicotinamide adenine dinucleotide (NADH), suggesting a surprising homology with eukaryotic organisms. The consequences of ROS cycling in immense aphotic zones representing key sites of nutrient regeneration and carbon export must now be considered, including potential control of carbon remineralization and metal bioavailability.

摘要

超氧阴离子和其他活性氧物质(ROS)源自多个自然来源,并深刻影响着包括碳和微量元素在内的众多元素循环。在深海中,由于长期缺乏光照,目前已知的 ROS 来源不复存在,但 ROS 的产生却神秘地发生了。在这里,我们表明,来自水生和陆地环境的具有多种分类和生态多样性的异养细菌是一个巨大的、未被认识到的、与光照无关的超氧阴离子来源,也许还有其他源自超氧阴离子的 ROS。普遍存在的玫瑰杆菌(Roseobacter)群中一种模式细菌的超氧阴离子产生涉及一种细胞外氧化还原酶,该酶受烟酰胺腺嘌呤二核苷酸(NADH)的还原形式刺激,这表明与真核生物存在惊人的同源性。现在必须考虑到在代表营养物质再生和碳输出关键地点的巨大无光区中 ROS 循环的后果,包括对碳再矿化和金属生物利用度的潜在控制。

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