Phytoremediation is one of the safer, economical, and environment-friendly techniques in which plants are used to recover polluted soils, particularly those containing toxic organic substances and heavy metals. However, it is considered as a slow form of remediation, as plants take time to grow and flourish. Various amendments, including the augmentation of certain chemical substances i.e., ethylenediamine tetraacetic acid (EDTA), ethylene glycol tetra acetic acid (EGTA), and sodium dodecyl sulfate (SDS) have been used to induce and enhance the phytoextraction capacity in plants. Several reports show that chemical amendments can improve the metal accumulation in different plant parts without actually affecting the growth of the plant. This raises a question about the amount and mechanisms of chemical amendments that may be needed for potentially good plant growth and metal phytoremediation. This review provides a detailed discussion on the mechanisms undertaken by three important chemical amendments that are widely used in enhancing phytoremediation (i.e., EDTA, EGTA, and SDS) to support plant growth as well as soil phytoremediation. A core part of this review focuses on the recent advances that have been made using chemical amendments in assisting metal phytoremediation.

Stem cell function in different meristems of Arabidopsis is mainly defined by WUSCHEL (WUS)/WUSCHEL-RELATED HOMEOBOX (WOX) family proteins. Sugars also have been demonstrated to play pivotal roles in stem cell function and development of plant. As a cytosolic fructose-1.6-bisphosphatase, FRUCTOSE INSENSITIVE1 (FINS1) has been demonstrated to regulate plant growth in response to fructose signaling. So far, it remains to be elucidated how stem cell function is regulated in response to fructose signaling. Our work showed that FINS1 interacts with WUS/WOX protein as a complex, which further binds to WUS/WOX promoter and regulates WUS/WOX expression in response to fructose signaling. FINS1 might act as a bifunctional factor that promotes WUS/WOX expression in the presence of low levels of fructose and represses WUS/WOX expression in the presence of high levels of fructose. Therefore, FINS1 regulates stem cell function in response to fructose signaling during the growth and development of Arabidopsis.

The auxin IAA is a vital plant hormone in controlling growth and development, but our knowledge about its complicated biosynthetic pathways and molecular regulation are still limited and fragmentary. cytokinin induced root waving 2 (ckrw2) was isolated as one of the auxin-deficient mutants in a large-scale forward genetic screen aiming to find more genes functioning in auxin homeostasis and/or its regulation. Here we show that CKRW2 is identical to Histone Monoubiquitination 1 (HUB1), a gene encoding an E3 ligase required for histone H2B monoubiquitination (H2Bub1) in Arabidopsis. In addition to pleiotropic defects in growth and development, loss of CKRW2/HUB1 function also led to typical auxin-deficient phenotypes in roots, which was associated with significantly lower expression levels of several functional auxin synthetic genes, namely TRP2/TSB1, WEI7/ASB1, YUC7 and AMI1. Corresponding defects in H2Bub1 were detected in the coding regions of these genes by chromatin immunoprecipitation (ChIP) analysis, indicating the involvement of H2Bub1 in regulating auxin biosynthesis. Importantly, application of exogenous cytokinin (CK) could stimulate CKRW2/HUB1 expression, providing an epigenetic avenue for CK to regulate the auxin homeostasis. Our results reveal a previously unknown mechanism for regulating auxin biosynthesis via HUB1/2-mediated H2Bub1 at the chromatin level.