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The inventory and chemical characterization of dissolved proteins in oceanic waters

机译:海洋水中溶解蛋白的清单和化学特征

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One-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and high resolution two-dimensional electrophoresis (2-DE) were applied to separate protein molecules in dissolved organic matter (DOM) from oceanic waters. Results were: (1) The 2-DE distinguished a total of 412 protein spots in 10 samples from five water columns over the Pacific, although fewer than 30 proteins were resolved as bands from the identical samples by SDS-PAGE. (2) Major and ubiquitous protein bands (34 and 39 kDa proteins) on the SDS-PAGE gel were resolved into horizontally spread arrays (trains) of spots on the 2-DE gels, indicating that these bands were a mixture of protein species that have the same molecular weight (MW) but different isoelectric points (pIs). (3) Proteins that exhibited such electrophoretic patterns on the 2-DE gels were glycosylated with variable linkages between the sugar and polypeptide chains. (4) N-terminal amino-acid sequencing demonstrated that individual spots within each train of spots had identical N-terminal amino-acid sequences. The N-terminal amino-acid sequences of the 39 and 34 kDa glycoprotein spots in samples collected at different sites were also identical. Protein isoforms with the same amino-acid sequence but different glycosylation profiles, termed glycoforms, were often observed on the 2-DE gel. Thirty-one and 24 spots on the 2-DE gels were glycoforms of two glycoproteins with MWs of 39 and 34 kDa, respectively; they were one protein species. The glycoforms of the 39 kDa protein were identified as a low molecular weight alkaline phosphatase (L-AP) of Pseudomonas aeruginosa PAO1 by a homology search through five amino-acid sequence databases. The present and earlier work indicates that all identified source organisms of dissolved proteins belong to the Pseudomonas group. We propose the hypothesis that proteins associated with membrane vesicles liberated from a minor member of the bacterioplankton assemblage, the marine Pseudomonas group, are one of the important sources of dissolved proteins in oceanic waters. This hypothesis may apply to the source pathway and survival not only of proteins and also to the universally occurring bacterial peptidoglycan and lipopolysaccharide components in DOM.
机译:一维十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和高分辨率二维电泳(2-DE)用于分离海洋水中溶解有机物(DOM)中的蛋白质分子。结果是:(1)2-DE在太平洋上5个水柱的10个样品中共分辨出412个蛋白斑点,尽管通过SDS-PAGE从相同样品中分离出的条带中只有不到30种蛋白质。 (2)将SDS-PAGE凝胶上的主要和普遍存在的蛋白条带(34和39 kDa蛋白)分解为2-DE凝胶上斑点的水平分布阵列(序列),表明这些条带是蛋白质种类的混合物,具有相同的分子量(MW)但具有不同的等电点(pIs)。 (3)在2-DE凝胶上表现出这种电泳模式的蛋白质被糖基化,并在糖和多肽链之间具有可变的连接。 (4)N末端氨基酸测序表明,每个斑点序列中的各个斑点具有相同的N末端氨基酸序列。在不同位点收集的样品中39和34 kDa糖蛋白斑点的N末端氨基酸序列也相同。通常在2-DE凝胶上观察到具有相同氨基酸序列但糖基化谱不同的蛋白质同工型,称为糖型。 2-DE凝胶上的31个斑点和24个斑点是两种糖蛋白的糖型,分子量分别为39和34 kDa。它们是一种蛋白质。通过五个氨基酸序列数据库的同源性搜索,将39 kDa蛋白的糖型鉴定为铜绿假单胞菌PAO1的低分子量碱性磷酸酶(L-AP)。当前和较早的工作表明,所有鉴定出的溶解蛋白来源生物都属于假单胞菌类。我们提出这样的假设:与膜小泡相关的蛋白质是从浮游细菌的次要成员海洋假单胞菌群中释放出来的,是海洋水中溶解蛋白质的重要​​来源之一。该假设不仅适用于蛋白质的来源途径和存活,而且适用于DOM中普遍存在的细菌肽聚糖和脂多糖成分。

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