Microplastics alter soil enzyme activities and microbial community structure without negatively affecting plant growth in an agroecosystem.

Despite the enormous benefits that plastics bring to our daily lives, plastics accumulate in the environment, especially microplastics (MPs; defined as particles <5 mm), which can cause many problems and potential loss of ecosystem services. Current research has shown the significant impact of MPs on aquatic systems, but little is known about their effect on terrestrial systems, especially within agroecosystems. Here, we investigated the effect of MPs types (PS, PE and PVC) on plant growth, soil enzyme activities, and microbial communities. MPs had a positive, type-dependent influence on plant growth affecting both above and below-ground productivity. MPs, especially PVC increased dry weights (+69.51 and + 164.62), and root length (+54.81) relative to control. Although the activity of ß-glucosidase, alkaline phosphatase, cellobiohydrolase, leucine-aminopeptidase, and dehydrogenase was suppressed by MPs except urease activity which was enhanced by MPs addition. The type of MPs in soil significantly altered C flow through the soil-plant system, indicating that MPs adversely affect many C-dependent soil functions. However, MPs (especially PVC) enhanced microbial biomass carbon (+14.88%) and altered the structure and metabolic status of the microbial community. MPs addition (especially PVC) greatly enhanced soil microbial structure (+29.59%; indicated by PLFAs) compared to control. Here we provide evidence that MPs can have significant effects on key pools and fluxes within the terrestrial C cycle, with responses being MPs type-dependent. Therefore, we concluded that MPs in soil are not benign and every step should be taken to restrict their access to the soil-plant system and their potential to transfer into the food chain.

Combined effect of salicylic acid and potassium mitigates drought stress through the modulation of physio-biochemical attributes and key antioxidants in wheat.

Improving physio-biochemical traits in wheat under drought stress conditions has received more research attention in recent years for better adaptability and higher yield. In this study, we explored the potential bio-physiological mechanisms underlying improved plant growth and water use efficiency in wheat following soil application of potassium (0 and 100 kg ha-1) and seed primed salicylic acid (SA) (150 mg per L) and SA foliar application (100 mg per L) under drought stresses (100%, 60% and 30% FC). Two years' average data revealed that inducing drought stress resulted in a decrease in plant pigments content, growth traits, and plant water status however, the influence was substantially reduced with the combined application of K and SA under drought stress conditions. The SA foliar spray in combination with K had increased chlorophyll a (174% and 83%), chl b (130% and 192%), chl a + b (156% and 120), carotenoid (22% and 11%), proline contents (24% and 29%) leaf relative water content (24% and 29%) while reduced leaf WSD (17% and 20%), WRC (6% and 7%), and WUC (23% and 28%) under mild and severe drought stresses, respectively. The increase in grain yield by 41% and 37% with enhanced water use efficiency was obtained with combined foliar SA and K under mild and severe drought stress, respectively indicating its vital role in overcoming the deleterious effects of drought via regulation of osmotic and metabolic processes and stabilizes cell components. RDA analysis revealed that the studied traits were completely discriminated under severe stress than mild or no drought stress. A positive and significant association was found between plant pigments with seed yield whereas a negative and significant correlation existed between water leaf traits and plant pigments. It was concluded that both foliar SA and seed primed SA with K fertilization combat the adverse effects of drought and improved plant water status as well as growth and bio-physiological traits of wheat under drought stress conditions.

Degradation of mitochondrial structure and deficiency of complex I were associated with the transgenic CMS of rice.

BACKGROUND: Mitochondria play a significant role in plant cytoplasmic male sterility (CMS). In our previous study, mitochondrial complex I genes, nad4, nad5, and nad7 showed polymorphisms between the transgenic CMS line M2BS and its wild type M2B. The sterility mechanism of the M2BS at cytological, physiological, biochemical, and molecular level is not clear. RESULTS: Cytological observation showed that the anthers were light yellow, fissured, invalid in KI-I2, and full of irregularly typical abortion pollen grains in M2BS. Transmission electron microscopic (TEM) observation revealed no nucleus and degraded mitochondria with obscure cristae in anther cells of M2BS. The results of staining for H2O2 presented a large number of electron dense precipitates (edp) in intercellular space of anther cells of M2BS at anthesis. Moreover, the anther respiration rate and complex I activity of M2BS were significantly lower than those of wild type M2B during pollen development. Furthermore, RNA editing results showed only nad7 presented partially edited at 534th nucleotides. The expression of nad5 and nad7 revealed significant differences between M2B and M2BS. CONCLUSIONS: Our data demonstrated that mitochondrial structural degradation and complex I deficiency might be associated with transgenic CMS of rice.

Identification of differentially expressed genes and pathways in isonuclear kenaf genotypes under salt stress.

Salinity is a potential abiotic stress and globally threatens crop productivity. However, the molecular mechanisms underlying salt stress tolerance with respect to cytoplasmic effect, gene expression, and metabolism pathway under salt stress have not yet been reported in isonuclear kenaf genotypes. To fill this knowledge gap, growth, physiological, biochemical, transcriptome, and cytoplasm changes in kenaf cytoplasmic male sterile (CMS) line (P3A) and its iso-nuclear maintainer line (P3B) under 200 mM sodium chloride (NaCl) stress and control conditions were analyzed. Salt stress significantly reduced leaf soluble protein, soluble sugars, proline, chlorophyll content, antioxidant enzymatic activity, and induced oxidative damage in terms of higher MDA contents in both genotypes. The reduction of these parameters resulted in a reduced plant growth compared with control. However, P3A was relatively more tolerant to salt stress than P3B. This tolerance of P3A was further confirmed by improved physio-biochemical traits under salt stress conditions. Transcriptome analysis showed that 4256 differentially expressed genes (DEGs) between the two genotypes under salt stress were identified. The Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis indicated that photosynthesis, photosynthesis antenna-protein, and plant hormone signal transduction pathways might be associated with the improved NaCl stress tolerance in P3A. Conclusively, P3A cytoplasmic male sterile could be a potential salt-tolerant material for future breeding program of kenaf and can be used for phytoremediation of salt-affected soils. These data provide a valuable resource on the cytoplasmic effect of salt-responsive genes in kenaf and salt stress tolerance in kenaf.

Degradation of mitochondrial structure and deficiency of complex I were associated with the transgenic CMS of rice

BACKGROUND: Mitochondria play a significant role in plant cytoplasmic male sterility (CMS). In our previous study, mitochondrial complex I genes, nad4, nad5, and nad7 showed polymorphisms between the transgenic CMS line M2BS and its wild type M2B. The sterility mechanism of the M2BS at cytological, physiological, biochemical, and molecular level is not clear. RESULTS: Cytological observation showed that the anthers were light yellow, fissured, invalid in KI-I2, and full of irregularly typical abortion pollen grains in M2BS. Transmission electron microscopic (TEM) observation revealed no nucleus and degraded mitochondria with obscure cristae in anther cells of M2BS. The results of staining for H2O2 presented a large number of electron dense precipitates (edp) in intercellular space of anther cells of M2BS at anthesis. Moreover, the anther respiration rate and complex I activity of M2BS were significantly lower than those of wild type M2B during pollen development. Furthermore, RNA editing results showed only nad7 presented partially edited at 534th nucleotides. The expression of nad5 and nad7 revealed significant differences between M2B and M2BS. CONCLUSIONS: Our data demonstrated that mitochondrial structural degradation and complex I deficiency might be associated with transgenic CMS of rice.

Identification of chalcone synthase genes and their expression patterns reveal pollen abortion in cotton.

Chalcone synthase (CHS) is a key enzyme and producing flavonoid derivatives as well play a vital roles in sustaining plant growth and development. However, the systematic and comprehensive analysis of CHS genes in island cotton (G. barbadense) has not been reported yet especially response to cytoplasmic male sterility (CMS). To fill this knowledge gap, a genome-wide investigation of CHS genes were studied in island cotton. A total of 20 GbCHS genes were identified and grouped into five GbCHSs. The gene structure analysis revealed that most of GbCHS genes consisted of two exons and one intron, and 20 motifs were identified. Twenty five pairs duplicated events (12 GbCHS genes) were identified including 23 segmental duplication pairs and two tandem duplication events, representing that GbCHS gene family amplification mainly owned to segmental duplication events and evolving slowly. Gene expression analysis exhibited that the GbCHS family genes presented a diversity expression patterns in various organs of cotton. Coupled with functional predictions and gene expression, the abnormal expression of GbCHS06, 10, 16 and 19 might be associated with pollen abortion of CMS line in island cotton. Conclusively, GbCHS genes exhibited diversity and conservation in many aspects, which will help to better understand functional studies and a reference for CHS research in island cotton and other plants.

Lead toxicity induced phytotoxic impacts on rapeseed and clover can be lowered by biofilm forming lead tolerant bacteria.

Lead (Pb+2) is a heavy metal and one of the main environmental pollutant, toxic to plants, animals and humans. Present study was conducted to evaluate ten plant growth promoting bacteria strains (B1-10) for biofilm production and their effect on growth indices, physiology, yield, antioxidant profile and lead uptake in rapeseed (Brassica napus) and clover (Trifolium repens) in lead polluted soil under nutrient broth medium and pot condition. Three pre-characterized biofilm forming lead tolerant growth promoting strains (B3: Pseudomonas fluorescens), B6: Pseudomonas putida and (B8: Bacillus safensis) were used to inoculate rapeseed and clover growing in the soil polluted with different levels (400, 800 and 1200 mg kg-1) of Pb arranged in completely randomized design with factorial arrangement. Results from screening experiment exhibited that more biofilm was produced by B3, B6 and B8 under highest level of lead contamination (1200 mg kg-1). Further, lead contamination decreased rapeseed and clover growth, physiology and yield at all levels of lead stress. But biofilm forming lead tolerant growth promoting bacteria application in lead contaminated soil enhanced rapeseed and clover growth, physiology, yield, antioxidant profile, proline and decreased malanodialdehyde content (which was decreased by different strains application under lead stress) of rapeseed and clover over no inoculation. Inoculation with all strains also increased the lead uptake in roots, shoots and decreased lead uptake in seeds of rapeseed and clover than plants in lead stress without inoculation.

Identification and analysis of RNA editing sites in chloroplast transcripts of kenaf (Hibiscus cannabinus L.).

RNA editing is one of the post-transcriptional modification processes and can lead to changes in sequencing and functioning of corresponding proteins and genetic information. To reveal the composition and characteristic of RNA editing of kenaf chloroplast genome, the RNA editing sites in kenaf chloroplast were predicted and identified using bioinformatics and RT-PCR analysis. The prediction results showed a total of 48 editing sites distributed in 22 genes, all of them were C to U conversion leading to amino acid changes. Further analysis of the position of RNA editing sites revealed that except 11 editing sites located at the first codon base, the other editing sites were found at the second codon base. Then four genes were randomly selected to validate the editing sites. Results showed that it was accurate to study the chloroplast RNA editing sites by bioinformatics method accompanied with cloning sequencing. Furthermore, the protein secondary structure and transmembrane domain of ndhD and atpA that had undergone gene editing also changed after editing. This implied that proteins with structural changes may have an impact on kenaf growth. Meanwhile, the differential editing site was found in chloroplast transcripts in kenaf CMS line and its maintainer line, indicating that chloroplast RNA editing could be associated with kenaf CMS. Therefore, the present study laid a foundation to further reveal the biological functioning of chloroplast RNA editing in CMS and its maintainer lines in kenaf.

Nitrogen nutrition in cotton and control strategies for greenhouse gas emissions: a review.

Cotton (Gossypium hirustum L.) is grown globally as a major source of natural fiber. Nitrogen (N) management is cumbersome in cotton production systems; it has more impacts on yield, maturity, and lint quality of a cotton crop than other primary plant nutrient. Application and production of N fertilizers consume large amounts of energy, and excess application can cause environmental concerns, i.e., nitrate in ground water, and the production of nitrous oxide a highly potent greenhouse gas (GHG) to the atmosphere, which is a global concern. Therefore, improving nitrogen use efficiency (NUE) of cotton plant is critical in this context. Slow-release fertilizers (e.g., polymer-coated urea) have the potential to increase cotton yield and reduce environmental pollution due to more efficient use of nutrients. Limited literature is available on the mitigation of GHG emissions for cotton production. Therefore, this review focuses on the role of N fertilization, in cotton growth and GHG emission management strategies, and will assess, justify, and organize the researchable priorities. Nitrate and ammonium nitrogen are essential nutrients for successful crop production. Ammonia (NH3) is a central intermediate in plant N metabolism. NH3 is assimilated in cotton by the mediation of glutamine synthetase, glutamine (z-) oxoglutarate amino-transferase enzyme systems in two steps: the first step requires adenosine triphosphate (ATP) to add NH3 to glutamate to form glutamine (Gln), and the second step transfers the NH3 from glutamine (Gln) to α-ketoglutarate to form two glutamates. Once NH3 has been incorporated into glutamate, it can be transferred to other carbon skeletons by various transaminases to form additional amino acids. The glutamate and glutamine formed can rapidly be used for the synthesis of low-molecular-weight organic N compounds (LMWONCs) such as amides, amino acids, ureides, amines, and peptides that are further synthesized into high-molecular-weight organic N compounds (HMWONCs) such as proteins and nucleic acids.