Enhanced Cd phytostabilization and rhizosphere bacterial diversity of Robinia pseudoacacia L. by endophyte Enterobacter sp. YG-14 combined with sludge biochar.

Robinia pseudoacacia L., a pioneer woody legume grown in mining areas, has been recognized as a remarkable accumulator of various heavy metals. Compared with other hazardous heavy metals (HMs), it is of low capacity in accumulating Cd, which, as a result, may hinder the phytoremediation efficiency. To enhance R. pseudoacacia's uptake efficiency of Cd, the individual effects of various rhizobia and arbuscular mycorrhizal fungi have been reported, however, the combined influence of endophytes and biochar receives little attention. In the current study, a Cd-adsorbing endophyte Enterobacter sp. YG-14 was inoculated to R. pseudoacacia, and its extraordinary effect on increasing R. pseudoacacia's Cd uptake was found, which was ascribed to the reinforced root Cd chelation by the strain through secreting siderophores/LMWOAs. Further, P-enriched sludge biochar was applied along with YG-14 to form a combined biochar-endophyte-accumulator system, in which biomineralization were reinforced (i.e. CdCO3 and Cd2P2O7 were generated), as the total and acid-soluble Cd in rhizosphere were reduced by 61.75% and 69.01% respectively, and soil's bacterial diversity was further improved with diversified N2-fixing microbial biomarkers. Multiple synergistic effects (E > 0) were also found, with the optimum performance on plant growth parameters (increased by 39.61%-561.91%) in comparison to the control group. Moreover, the system exhibited a preferable Cd phytostabilization capacity with the highest increase (81.42%) in Cd accumulation and a significant reduction (72.73%) in Cd root-to-shoot translocation.

Withanolides isolated from Tubocapsicum anomalum and their antiproliferative activity.

Seven undescribed withanolides (1-7) and six artificial withanolides (8-13), along with 20 known compounds (14-33) were isolated from the aerial parts of Tubocapsicum anomalum. Their structures were confirmed by comprehensive spectroscopic analyses. The absolute configuration of compound 1 was defined by single-crystal X-ray crystallography. All isolates were evaluated for their antiproliferative effects against five human tumor cell lines (Hep3B, MDA-MB-231, SW480, HCT116 and A549), among which compound 24 (tubocapsanolide A) exhibited the highest activities against the MDA-MB-231 cells with an IC50 value of 1.89 ± 1.03 µM. Further studies showed that 24 exhibited significant damage to mitochondria in MDA-MB-231 cells, including excess reactive oxygen species, decreased mitochondrial membrane potential, and apoptosis initiation. In addition, compound 24 also inhibited cell migration. These findings show that tubocapsanolide A may be a promising molecule for triple-negative breast cancer treatment and merit further evaluation.