Department of Genome Sciences, University of Washington, Seattle, Washington, United States of America ; Medicinal Chemistry Department, University of Washington, Seattle, Washington, United States of America.
PLoS One. 2013 Oct 16;8(10):e75653. doi: 10.1371/journal.pone.0075653. eCollection 2013.
Phytoplankton growth rates are limited by the supply of iron (Fe) in approximately one third of the open ocean, with major implications for carbon dioxide sequestration and carbon (C) biogeochemistry. To date, understanding how alteration of Fe supply changes phytoplankton physiology has focused on traditional metrics such as growth rate, elemental composition, and biophysical measurements such as photosynthetic competence (Fv/Fm). Researchers have subsequently employed transcriptomics to probe relationships between changes in Fe supply and phytoplankton physiology. Recently, studies have investigated longer-term (i.e. following acclimation) responses of phytoplankton to various Fe conditions. In the present study, the coastal diatom, Thalassiosira pseudonana, was acclimated (10 generations) to either low or high Fe conditions, i.e. Fe-limiting and Fe-replete. Quantitative proteomics and a newly developed proteomic profiling technique that identifies low abundance proteins were employed to examine the full complement of expressed proteins and consequently the metabolic pathways utilized by the diatom under the two Fe conditions. A total of 1850 proteins were confidently identified, nearly tripling previous identifications made from differential expression in diatoms. Given sufficient time to acclimate to Fe limitation, T. pseudonana up-regulates proteins involved in pathways associated with intracellular protein recycling, thereby decreasing dependence on extracellular nitrogen (N), C and Fe. The relative increase in the abundance of photorespiration and pentose phosphate pathway proteins reveal novel metabolic shifts, which create substrates that could support other well-established physiological responses, such as heavily silicified frustules observed for Fe-limited diatoms. Here, we discovered that proteins and hence pathways observed to be down-regulated in short-term Fe starvation studies are constitutively expressed when T. pseudonana is acclimated (i.e., nitrate and nitrite transporters, Photosystem II and Photosystem I complexes). Acclimation of the diatom to the desired Fe conditions and the comprehensive proteomic approach provides a more robust interpretation of this dynamic proteome than previous studies.
浮游植物的生长速度受到铁(Fe)供应的限制,大约有三分之一的开阔海域都存在这种情况,这对二氧化碳的封存和碳(C)生物地球化学有重大影响。迄今为止,人们对Fe 供应变化如何改变浮游植物生理学的理解主要集中在传统指标上,如生长速率、元素组成和生物物理测量,如光合能力(Fv/Fm)。研究人员随后采用转录组学来探究 Fe 供应变化与浮游植物生理学之间的关系。最近,研究人员研究了浮游植物对各种 Fe 条件的长期(即适应后)反应。在本研究中,沿海硅藻拟菱形藻经过低 Fe 或高 Fe 条件(即 Fe 限制和 Fe 充足)的适应(10 代)。定量蛋白质组学和一种新开发的蛋白质组学分析技术,用于鉴定低丰度蛋白质,用于检查硅藻在两种 Fe 条件下表达的全部蛋白质组,从而检查其代谢途径。总共鉴定出 1850 种蛋白质,几乎是以前从硅藻差异表达中鉴定出的蛋白质的三倍。拟菱形藻有足够的时间适应 Fe 限制,上调与细胞内蛋白质再循环相关的途径中的蛋白质,从而减少对细胞外氮(N)、C 和 Fe 的依赖。光呼吸和戊糖磷酸途径蛋白丰度的相对增加揭示了新的代谢转变,这些转变创造了可以支持其他成熟生理反应的底物,例如在 Fe 限制的硅藻中观察到的高度硅化的壳。在这里,我们发现,在短期 Fe 饥饿研究中观察到下调的蛋白质及其途径在拟菱形藻适应时被组成型表达(即硝酸盐和亚硝酸盐转运蛋白、光系统 II 和光系统 I 复合物)。硅藻对所需 Fe 条件的适应和全面的蛋白质组学方法提供了比以前的研究更稳健的动态蛋白质组解释。