“…So far, only one study on proteome profiling in Fe-deficient rice roots and shoots (Chen et al, 2015) and two in maize, with one in Fe-deficient root hairs (Li et al, 2015) and the other in roots (Hopff et al, 2013), have been carried out to investigate the global protein changes or the alterations in the plasma membrane proteome, by means of two-dimensional electrophoresis (2-DE), or 1-DE coupled with matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF/MS) or LC-MS/MS. By contrast, most of the proteomic studies upon Fe deficiency have been performed in Strategy I species, including Beta vulgaris (Andaluz et al, 2006; Rellan-Alvarez et al, 2010; Gutierrez-Carbonell et al, 2016), Tomato ( Solanum lycopersicum L.) (Brumbarova et al, 2008; Genannt Bonsmann et al, 2008; Muneer and Jeong, 2015), cucumber ( Cucumis sativus ) (Donnini et al, 2010; Li and Schmidt, 2010; Vigani et al, 2017), pea ( Pisum sativum L.) (Meisrimler et al, 2011, 2016), Prunus hybrid GF 677 rootstock ( P. dulcis × P. persica ) (Rodriguez-Celma et al, 2013a), Lupinus texensis (Lattanzio et al, 2013), Hyoscyamus albus (Khandakar et al, 2013), Medicago truncatula (Rodriguez-Celma et al, 2011, 2016), citrus rootstocks (Muccilli et al, 2013), Brassica napu (Gutierrez-Carbonell et al, 2015), Populus cathayana (Zhang S. et al, 2016), and Arabidopsis (Laganowsky et al, 2009; Lan et al, 2011, 2012b; Mai et al, 2015; Pan et al, 2015; Zargar et al, 2015a,b). Most of the protein profiling studies were focused on the global protein changes in the whole roots/shoots, and few of them investigated proteome of the specific plant parts such as root hairs (Li et al, 2015), cellular compartments including root plasma membrane (Hopff et al, 2013), thylakoid membranes (Andaluz et al, 2006), and shoot microsomal fragments (Zargar et al, 2015b), as well as phloem saps (Lattanzio et al, 2013; Gutierrez-Carbonell et al, 2015).…”