Chromium (Cr) contamination poses food safety and environmental challenges, yet the early-stage physiological and molecular responses to Cr(III) stress remain unclear. Citrus and tomato are economically important crops representing woody and herbaceous species, making them valuable models for studying heavy metal toxicity in plants. This study investigates the impact of Cr (III) exposure on citrus and tomato seedlings, with a focus on physiological phenotypes and transcriptional response. Citrus seed germination declines with increasing Cr(III) concentrations, while low Cr(III) levels promote tomato germination, with inhibition occurring above 1 g/L. Under hydroponic conditions, Cr (III) severely hampers root and leaf growth in both citrus and tomato plants, accompanied by decreased net photosynthetic rate. Using a GFP-based confocal microscopy system, we observed reduced fluorescence intensity within three days of Cr(III) exposure (100 mg/L and 500 mg/L), indicating early cellular damage. Biochemical assays revealed oxidative stress, marked by increased H2O2, malondialdehyde (MDA), and antioxidant enzyme activity. Additionally, low Cr (III) concentrations could result in the death of various microorganisms, including Escherichia coli, Agrobacterium rhizogenes, and Agrobacterium tumefaciens. Transcriptomic analysis identified differentially expressed genes related to MAPK signaling pathway and Plant hormone signal transduction pathway. Transcription of many transcription factors, such as bHLH, WRKY, and MYB, also underwent significant changes.

Drought and soil salinization significantly constrain agricultural productivity, driving the need for molecular breeding strategies to enhance stress resistance. Zinc finger proteins play a critical role in plant response to abiotic stress. In this study, a gene encoding a C2H2-type zinc finger protein (AfZFP5) was cloned from Amorpha fruticosa, a species known for its strong adaptability. qRT-PCR analysis revealed that AfZFP5 expression is regulated by sorbitol, H2O2, NaCl, and NaHCO3. And all four treatments can cause upregulation of AFZFP5 expression in the roots or leaves of Amorpha fruticosa within 48 h. Transgenic tobacco lines overexpressing AfZFP5 demonstrated enhanced tolerance to drought and salt-alkali stress at germination, seedling, and vegetative stages. Compared to wild-type plants, transgenic lines exhibited significantly higher germination rates, root lengths, and fresh weights when treated with sorbitol, NaCl, and NaHCO3. Under natural drought and salt-alkali stress conditions, transgenic plants showed elevated activities of superoxide dismutase (SOD) and peroxidase (POD), and upregulated expression of oxidative stress-related kinase genes (NtSOD, NtPOD) during the vegetative stage. Additionally, transgenic tobacco displayed lower malondialdehyde (MDA) content and reduced staining levels with 3,3 ' diaminobenzidine (DAB) and Nitro blue tetrazolium (NBT), indicating enhanced reactive oxygen species (ROS) scavenging capacity by AfZFP5 upon salt-alkali stress. Under simulated drought with PEG6000 and salt-alkali stress, chlorophyll fluorescence intensity and Fv/Fm values in transgenic tobacco were significantly higher than in wild-type plants during the vegetative stage, suggesting that AfZFP5 mitigates stress-induced damage to the photosynthetic system. This study highlights the role of AfZFP5 in conferring drought and salt-alkali stress tolerance, providing genetic resources and a theoretical foundation for breeding stress-resistance crops.

The prerequisite for breeding a plant to be used in phytoremediation is its high tolerance to grow normally in soil contaminated by certain heavy metals. As mechanisms of plant uptake and transport of nickel (Ni) are not fully understood, it is of significance to utilize exogenous genes for improving plant Ni tolerance. In this study, rcnA from Escherichia coli encoding an exporter of Ni and cobalt was overexpressed constitutively in Arabidopsis thaliana, and the performance of transgenic plants was assayed under Ni stress. The subcellular localization of rcnA in plant cells was found to be the plasma membrane. Constitutive overexpression of rcnA in Arabidopsis rendered better growth of either seedlings on agar medium containing 85, 100, and 120 mu M NiCl2 or adult plants in a nutrient solution with 5 mM NiCl2 added. Compared to the wildtype, rcnA-OE transgenic plants under Ni stress accumulated lower levels of reactive oxygen species (i.e., superoxide and hydrogen peroxide) in leaves and exhibited less oxidative damage in shoots, as demonstrated by less electrolyte leakage and the lower malondialdehyde content. Notably, rcnA-OE transgenic plants retained a higher content of Ni in roots and had a lower content of Ni in shoots. Therefore, our findings indicated that the bacterial rcnA gene may be utilized to improve plant Ni tolerance through genetic transformation.