Sutak Robert, Camadro Jean-Michel, Lesuisse Emmanuel
Department of Parasitology, Faculty of Science, Charles University, BIOCEV, Vestec, Czechia.
CNRS, Institut Jacques Monod, Université de Paris, Paris, France.
Front Microbiol. 2020 Nov 5;11:566691. doi: 10.3389/fmicb.2020.566691. eCollection 2020.
Oceanic phytoplankton species have highly efficient mechanisms of iron acquisition, as they can take up iron from environments in which it is present at subnanomolar concentrations. In eukaryotes, three main models were proposed for iron transport into the cells by first studying the kinetics of iron uptake in different algal species and then, more recently, by using modern biological techniques on the model diatom . In the first model, the rate of uptake is dependent on the concentration of unchelated Fe species, and is thus limited thermodynamically. Iron is transported by endocytosis after carbonate-dependent binding of Fe(III)' (inorganic soluble ferric species) to phytotransferrin at the cell surface. In this strategy the cells are able to take up iron from very low iron concentration. In an alternative model, kinetically limited for iron acquisition, the extracellular reduction of all iron species (including Fe') is a prerequisite for iron acquisition. This strategy allows the cells to take up iron from a great variety of ferric species. In a third model, hydroxamate siderophores can be transported by endocytosis (dependent on ISIP1) after binding to the FBP1 protein, and iron is released from the siderophores by FRE2-dependent reduction. In prokaryotes, one mechanism of iron uptake is based on the use of siderophores excreted by the cells. Iron-loaded siderophores are transported across the cell outer membrane via a TonB-dependent transporter (TBDT), and are then transported into the cells by an ABC transporter. Open ocean cyanobacteria do not excrete siderophores but can probably use siderophores produced by other organisms. In an alternative model, inorganic ferric species are transported through the outer membrane by TBDT or by porins, and are taken up by the ABC transporter system FutABC. Alternatively, ferric iron of the periplasmic space can be reduced by the alternative respiratory terminal oxidase (ARTO) and the ferrous ions can be transported by divalent metal transporters (FeoB or ZIP). After reoxidation, iron can be taken up by the high-affinity permease Ftr1.
海洋浮游植物物种具有高效的铁获取机制,因为它们能够从铁浓度处于亚纳摩尔水平的环境中摄取铁。在真核生物中,通过首先研究不同藻类物种中铁摄取的动力学,以及最近在模式硅藻上使用现代生物技术,提出了三种主要的铁转运进入细胞的模型。在第一个模型中,摄取速率取决于未螯合的铁物种的浓度,因此在热力学上受到限制。在细胞表面,Fe(III)'(无机可溶性铁物种)与植物转铁蛋白发生碳酸盐依赖性结合后,铁通过内吞作用进行转运。在这种策略中,细胞能够从极低的铁浓度中摄取铁。在另一种模型中,铁获取在动力学上受到限制,所有铁物种(包括Fe')的细胞外还原是铁获取的先决条件。这种策略使细胞能够从多种铁物种中摄取铁。在第三个模型中,异羟肟酸铁载体与FBP1蛋白结合后,可通过内吞作用(依赖于ISIP1)进行转运,铁通过FRE2依赖性还原从铁载体中释放出来。在原核生物中,一种铁摄取机制基于细胞分泌的铁载体的使用。负载铁的铁载体通过TonB依赖性转运蛋白(TBDT)穿过细胞外膜,然后通过ABC转运蛋白转运到细胞内。开阔海洋中的蓝细菌不分泌铁载体,但可能利用其他生物产生的铁载体。在另一种模型中,无机铁物种通过TBDT或孔蛋白穿过外膜,并被ABC转运蛋白系统FutABC摄取。或者,周质空间中的三价铁可以被交替呼吸末端氧化酶(ARTO)还原,二价金属转运蛋白(FeoB或ZIP)可以转运亚铁离子。再氧化后,铁可以被高亲和力通透酶Ftr1摄取。