Objective: This study was conducted to identify the phytochemical constituents of Leucaena leucocephala leaf extracts using gas chromatographymass spectrometry (GC-MS).Methods: Hexane, petroleum ether, chloroform, ethyl acetate and methanol leaves extract of L. leucocephala were analyzed using GC-MS, while the mass spectra of the compounds found in the extract were matched with the National Institute of Standards and Technology (NIST) library.Results: GC-MS analysis of L. leucocephala leaves revealed the presence of 30 compounds and the major chemical constituents were Squalene (41.02%), Phytol (33.80%), 3,7,11,15-Tetramethyl-2-hexadecen-1-ol (30.86%) and 3,7,11-Tridecatrienenitrile, 4,8,12-trimethyl (25.64%). Some of these compounds have been reported to possess various biological activities such as antioxidant, antimicrobial, hepatoprotective, antiparasitic, insecticide, nematicide, pesticide, anti coronary, antiarthritic, antiandrogenic, hypocholesterolemic, cancer preventive, anti-cancer, analgesic, anesthetic, allergenic and etc. Conclusion:The findings of this study indicating that L. leucocephala leaves possess various potent bioactive compounds and is recommended as a plant of phytopharmaceutical importance.

Polysaccharides in carob fruit, including carob bean gum (also known as carob gum, locust bean gum) and carob fiber, are widely used in industries such as food, pharmaceuticals, paper, textile, oil well drilling and cosmetics. Carob bean gum is a galactomannan obtained from the seed endosperm of carob tree and the fiber is obtained by removing most of soluble carbohydrates in carob pulp by water extraction. Both the gum and fiber are beneficial to health for many diseases such as diabetes, bowel movements, heart disease and colon cancer. This article reviewed the composition, properties, food applications and health benefits of polysaccharides from carob fruit.

The seeds of Jatropha curcas contain a high percentage of biodiesel. However, low seed yield which was limited by its poor female flowers was a bottleneck for its utilization. Here, we compared the transcriptomic profiles of five different samples during floral sex differentiation stages using Illumina Hiseq 4000. Our results showed that hundreds of differentially expressed genes (DEGs) were detected in floral sex initiation period, but thousands of DEGs were involved in the stamens and ovules development process. Moreover, the DEGs were mainly shown up-regulation in male floral initiation, but mainly down-regulation in female floral initiation. Male floral initiation was associated with the flavonoid biosynthesis pathway while female floral initiation was related to the phytohormone signal transduction pathway. Cytokinin (CTK) signaling triggered the initiation of female floral primordium, thereafter other phytohormones co-promoted the female floral development. In addition, the floral organ identity genes played important roles in floral sex differentiation process and displayed a general conservation of the ABCDE model in J. curcas. To the best of our knowledge, this data is the first comprehensive analysis of the underlying regulatory mechanism and the related genes during floral sex differentiation in J. curcas, which help in engineering high-yielding varieties of J. curcas.

In the present work, for the first time, the chemical components of essential oils (EOs) and extracts from wood branch (WB) resulted from the tree pruning wastes of Schinus molle L. grown in Egypt were evaluated for their antioxidant and antibacterial activities. EOs, methanol (ME), dichloromethane (DCME) and water (WE) extracts as antioxidant and antibacterial activities were measured. Total phenolic and flavonoid contents as well as analysis of extracts by gas chromatography-mass spectrometry (GC-MS) were reported. The major components in EOs were a-elemol, b-pinene, and a-phellandrene, in ME were 6-(4-chlorophenyl)-3-cyano-4-(N-benzylpiperazino)-2H-pyran-2-one, and 2-naphthalene methanol, decahydro-a,a,4a-trimethyl-8-methylene, in DCME were 12-methyl-E,E-3,13-octadecadien-1-ol, and 1,2-benzenedicarboxylic acid, dioctyl ester, and in WE were beudesmol, and (Z,Z,Z)-9,12,15-octadecatrienoic acid, 2,3dihydroxypropyl ester. The highest total antioxidant activity was found with EOs (90 ± 1.23 %) and WE (86.30 ± 1.40 %). The lowest IC 50 values of 13.11 ± 3.00, and 12.66 ± 2.15 lg/mL were found with WE and EOs, respectively. EOs and WE were observed to have good antibacterial activity against Bacillus subtilis, Bacillus cereus, Staphylococcus aureus, Escherichia coli, Sarcina lutea, Pseudomonas aeruginosa, and Micrococcus luteus. In conclusion, the Schinus molle L. WB EOs and extracts might, indeed, be used as a potential source for pharmaceutical or food industries.

Jatropha curcas L. seeds an oilseed plant with great potential for biodiesel production. However, low seed yield, which was limited by its lower female flowers, was a major drawback for its utilization. Our previous study found that the flower number and female-to-male ratio were increased by gibberellin treatment. Here, we compared the transcriptomic profiles of inflorescence meristem at different time points after gibberellic acid A3 (GA3) treatment. The present study showed that 951 differentially expressed genes were obtained in response to gibberellin treatment, compared with control samples. The 6-h time point was an important phase in the response to exogenous gibberellin. Furthermore, the plant endogenous gibberellin, auxin, ethylene, abscisic acid, and brassinolide-signaling transduction pathways were repressed, whereas the genes associated with cytokinin and jasmonic acid signaling were upregulated for 24-h time point following GA3 treatment. In addition, the floral meristem determinacy genes (JcLFY, JcSOC1) and floral organ identity genes (JcAP3, JcPI, JcSEP1-3) were significantly upregulated, but their negative regulator (JcSVP) was downregulated after GA3 treatment. Moreover, the effects of phytohormone, which was induced by exogenous plant growth regulator, mainly acted on the female floral differentiation process. To the best of our knowledge, this data is the first comprehensive analysis of the underlying transcriptional response mechanism of floral differentiation following GA3 treatment in J. curcas, which helps in engineering high-yielding varieties of Jatropha.

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Leucaena leucocephala trees are commonly known as White Lead tree. It is native to Southern Mexico and Northern Central America and spread across many tropical and sub-tropical locations. It has multipurpose uses, such as generation of firewood, timber, greens, fodder, and green manure, as well as to provide shade and control soil erosion. It has been used for medicinal purposes because of possessing multiple pharmacological properties. Studies have shown the presence of various secondary metabolites such as alkaloid, cardiac glycosides, tannins, flavonoids, saponins, and glycosides in this species. In traditional medicine, it is used to control stomach ache and as contraception and abortifacient. In the present study, the global distribution, taxonomy, chemical composition, pharmacological activities, and potential uses of Leucaena leucocephalaare discussed.

This work, for the first time, identified the phytochemical constituents of leaves, fruits, stem barks, and wood branches extracted from the tree pruning wastes of Leucaena leucocephala (Lam.) de Wit. grown in Egypt, showing 49, 29, 34, and 27 phytocomponents, respectively, as assayed by gas chromatograph-mass spectroscopy (GC-MS) analysis. The major components of leaves were 1,2-benzenedicarboxylic acid, mono(2-ethylhexyl) ester (17.7%), betulin (15.7%), lupeol (14.7%), androstan-17-one,3-ethyl-3-hydroxy-, (5à)- (12.3%), 9,12,15-octadecatrienoic acid, methyl ester, (Z,Z,Z)- (11.6%), betamethasone (9.7%), and β-sitosterol (9.1%). The major phytocomponents of fruits were β-sitosterol (55.7%), 3beta-hydroxy-5-cholen-24-oic acid (48.7%), 1,2-benzenedicarboxylic acid, mono(2-ethylhexyl) ester (42.9%), lupeol (29.3%), betulin (15.8%), stigmasterol (12.8%), and campesterol (7.6%). The major phytocomponents of stem barks were 1,2-benzenedicarboxylic acid, diisooctyl ester (65.7%), β-sitosterol (27.2%), betulin (22.1%), lupeol (21.1%), and 9,12-octadecadienoic acid (Z,Z)-, methyl ester (8.8%). Wood branches contained β-sitosterol (60.1%), 1,2-benzenedicarboxylic acid, mono(2-ethylhexyl) ester (47.2%), lupeol (22.5%), campesterol (15.6%), and stigmasterol (14.1%). Most of the identified compounds have been reported to possess important biological activities, such as antimicrobial, anti-inflammatory, anticancer, anti-arthritic, antioxidant, and antidiabetic activities. The four constituents of L. leucocephala were statistically independent in these phytocomponents. The phytocomponents in five solvents were mixed in describing the four constituents. These constituents of L. leucocephala are potential bioresources for phytopharmaceutics.