Some of the essential polyunsaturated fatty acids (PUFAs) as ARA (arachidonic acid, n-6), EPA (eicosapentaenoic acid, n-3) and DHA (Docosahexaenoic acid, n-3) cannot be synthesized by mammals and it must be provided as food supplement. ARA and DHA are the major PUFAs that constitute the brain membrane phospholipid. n-3 PUFAs are contained in fish oil and animal sources, while the n-6 PUFAs are mostly provided by vegetable oils. Inappropriate fatty acids consumption from the n-6 and n-3 families is the major cause of chronic diseases as cancer, cardiovascular diseases and diabetes. The n-6: n-3 ratio (lower than 10) recommended by the WHO can be achieved by consuming certain edible sources rich in n-3 and n-6 in daily food meal. Many researches have been screened for alternative sources of n-3 and n-6 PUFAs of plant origin, microbes, algae, lower and higher plants, which biosynthesize these valuable PUFAs needed for our body health. Biosynthesis of C18 PUFAs, in entire plant kingdom, takes place through certain pathways using elongases and desaturases to synthesize their needs of ARA (C20-PUFAs). This review is an attempt to highlight the importance and function of PUFAs mainly ARA, its occurrence throughout the plant kingdom (and others), its biosynthetic pathways and the enzymes involved. The methods used to enhance ARA productions through environmental factors and metabolic engineering are also presented. It also deals with advising people that healthy life is affected by their dietary intake of both n-3 and n-6 FAs. The review also addresses the scientist to carry on their work to enrich organisms with ARA.

Uric acid increased accumulation and/or reduced excretion in human bodies is closely related to pathogenesis of gout and hyperuricemia. It is highly affected by the high intake of food rich in purine. Uric acid is present in both higher plants and microorganisms with species dependent concentration. Urate-degrading enzymes are found both in plants and microorganisms but the mechanisms by which plant degrade uric acid was found to be different among them. Higher plants produce various metabolites which could inhibit xanthine oxidase and xanthine oxidoreductase, so prohibit the oxidation of hypoxanthine to xanthine then to uric acid in the purine metabolism. However, microorganisms produce group of degrading enzymes uricase, allantoinase, allantoicase and urease, which catalyze the degradation of uric acid to the ammonia. In humans, researchers found that several mutations caused a pseudogenization (silencing) of the uricase gene in ancestral apes which exist as an insoluble crystalloid in peroxisomes. This is in contrast to microorganisms in which uricases are soluble and exist either in cytoplasm or peroxisomes. Moreover, many recombinant uricases with higher activity than the wild type uricases could be induced successfully in many microorganisms. The present review deals with the occurrence of uric acid in plants and other organisms specially microorganisms in addition to the mechanisms by which plant extracts, metabolites and enzymes could reduce uric acid in blood. The genetic and genes encoding for uric acid in plants and microorganisms are also presented.

The effects of silver nanoparticles (AgNPs), silver ions (Ag⁺), and polyvinylpyrrolidone (PVP) on mitosis and expression of gene encoding cyclin-dependent kinase 2 (cdc2) in onion roots were compared. Three concentrations (5, 10, and 15 mg dm^-3) were employed in combination with three incubation times (3, 6, and 9 h). PVP enhanced mitotic index and cdc2 expression. Both silver forms decreased mitotic index and cdc2 expression. Genotoxicity of both silver forms were indicated by three major distinguishable classes of chromosome aberrations: spindle disturbances, clastogenic aberrations, and chromosome stickiness. Concerning Ag⁺ treatments, significant enhancements in occurrence of any chromosome aberration type was associated with significant decrease in mitotic index. On the other hand, disturbed spindle in AgNPs treatments was observed even in absence of significant reduction in mitotic index suggesting that AgNPs inhibit cellular events occurring during mitosis to proceed normally rather than starting of cell division.

The pollution of freshwater resources with crude petroleum oil is a major environmental issue in oil-producing countries. As a result, the remediation of polluted aquatic ecosystems using eco-friendly and cost-effective technology is receiving increased global attention. In this study, the ability of Azolla pinnata R. Br. to remediate petroleum-polluted freshwater was assessed. The remediation potentiality was determined by evaluating the total petroleum hydrocarbon degradation percentage (TPH%) and changes in the molecular type composition of saturated and aromatic hydrocarbon fractions. TPH% was estimated gravimetrically, and changes in the molecular type composition of saturated and aromatic fractions were measured using gas chromatography and high-performance liquid chromatography, respectively. The results reveal that A. pinnata has the potential to phytoremediate freshwater polluted with low levels (up to 0.5 g/L) of petroleum hydrocarbons (PHs). After seven days of phytoremediation, the degradation rate of total PHs was 92% in the planted treatment compared with 38% in the unplanted positive control. The highest breakdown of PHs for the normal paraffinic saturated hydrocarbon fraction occurred in the presence of A. pinnata combined with Anabena azollaea (A-A), which showed a moderate degradation capacity toward total aromatic hydrocarbons (TAHs) and total polycyclic aromatic hydrocarbons (PAHs). The results indicate that A. pinnata effectively removed C18, a saturated PH, and acenaphthene (Ace), an aromatic PH. Therefore, this study suggests that A. pinnata is a useful tool for the remediation of freshwaters contaminated with low pollution levels of crude oil.

In oil-producing countries, water pollution by crude petroleum oil frequently occurs and causes many environmental problems. This study aims to investigate the effect of crude petroleum oil on the growth and functional trails of the economically important freshwater plant Azolla pinnata R. Br. and to report on the plant’s resistance to this abiotic stress. Plants were raised in an open greenhouse experiment under different levels of crude oil pollution ranging from 0.5 to 2.0 g/L. Plant functional traits were monitored over a three-week period. Plant cover of A. pinnata was decreased with the increased levels of oil pollution. The total chlorophyll content decreased from 0.76 mg/g fresh weight under 2 g/L oil treatment after 21 days of growth. The chlorophyll a/b ratio exceeded the unity at crude oil treatments above 1 g/L, with values reaching 2.78 after seven days, while after 21 days, the ratio ranged from 1.14 to 1.31. The carotenoid content ranged from 0.17 mg/g in the control to 0.11 mg/g in the 2 g/L oil treatment. The carotenoid content varied over time in relation to DNA% damage, which increased from 3.63% in the control to 11.36% in the highest oil treatment level of 2 g/L. The crude oil stress caused severe damage in the frond tissues and chloroplast structure of A. pinnata, including a less compacted palisade, the malformation of the epidermis, the disintegration of parenchyma tissue, and the lysis and malformation of the chloroplasts. Since A. pinnata cannot withstand high concentrations of crude oil pollution, it is for use in the remediation of slightly polluted freshwaters up to 0.5 g/L.

The target of this study is to use Allium cepa roots as model to evaluate the potential use of three antioxidants scavengers [vitamin C (VC), vitamin E (VE) and butylated hydroxytoluene (BHT)] ,either singly or in combination, in mitigation of of genotoxic and cytotoxic effects of silver nanoparticles (AgNPs). The results indicated that AgNPs manifested mitodepressive and genotoxic symptoms, represented as decrease in mitotic index (MI), elevated total chromosome aberrations (TCA) and tail DNA (tDNA), associated with oxidative stress markers represented by increase in malonaldehyde (MDA) and hydrogen peroxide (H2O2) contents. Each of VC, VE and 1:1:1 mix of VC, VE and BHT ameliorated the harmful effects of AgNPs with best performance recorded for VE. Though, BHT decreased AgNPs-generated MDA and H2O2; it enforced the mitodepressive and genotoxic properties associated with application of nanoparticles. The results also reflected superiority of pretreatment over co-treatment with antioxidants in mitigation of the AgNPs-associated hazards.