Development and Characterization of Eco-Friendly Non-Isocyanate Urethane Monomer from Jatropha curcas Oil for Wood Composite Applications

The aim of this research work was to evaluate the potential of using renewable natural feedstock,i.e.,Jatropha curcas oil(JCO)for the synthesis of non-isocyanate polyurethane(NIPU)resin for wood composite applications.Commercial polyurethane(PU)is synthesized through a polycondensation reaction between isocyanate and poly-ol.However,utilizing toxic and unsustainable isocyanates for obtaining PU could contribute to negative impacts on the environment and human health.Therefore,the development of PU from eco-friendly and sustainable resources without the isocyanate route is required.In this work,tetra-n-butyl ammonium bromide was used as the activator to open the epoxy ring with 3-Aminopropyltriethoxisylane as a catalyst to yield urethane of JCO(UJCO).The UJCO were characterized by Fourier Transform Infra-Red spectroscopy(FTIR)and their oxirane,and hydroxyl values were measured.The result showed that a decrease in oxirane value was found while the hydroxyl value was increased during the time,confirming that the urethane group was formed.The presence of functional groups in FTIR spectra at wave numbers 1732.08,1562.34,and 3348.42 cm^(−1) indicates the functional groups of C=O(urethane carbonyl),–NH,and–OH,respectively confirmed this finding.The potential applications of NIPU in the wood composite were also outlined.

Effect of Water Deficit Stress on Photosynthetic Characteristics of Jatropha curcas

The need to mitigate climate change cannot be more emphasized, which arises, as a result of increases in CO2 emissions due to anthropogenic activities. Given the current world energy problems of high fossil fuel consumption which plays a pivotal role in the greenhouse effect, Jatropha curcas biodiesel has been considered a potential alternative source of clean energy (biodiesel is carbon neutral). However, the ability of Jatropha curcas, as a candidate source of alternative of clean energy, to grow in marginal and dry soils, has been poorly elucidated. This study, therefore aimed at investigating whether Jatropha curcas leaves could switch from carrying out C3 photosynthetic pathway to Crassulacean Acid Metabolism (CAM) as a strategy to improve its water deficit tolerance. Thirty-five-day-old Jatropha curcas accessions, from three different climatic zones of Botswana, viz., Mmadinare (Central zone), Thamaga (Southern zone) and Maun (Northern zone), were subjected to water stress, by with-holding irrigation with half-strength Hoagland culture solution. Net photosynthetic rate, transpiration and stomatal conductance were measured at weekly intervals. The leaf pH was measured to determine whether there was a decrease in pH (leaf acidification) of the leaves during the night, when the plants experienced water deficit stress. All the accessions exhibited marked reduction in all the measured photosynthetic characteristics when experience water deficit stress. However, a measurable CO2 uptake was carried out by leaves of all the accessions, in the wake of marked decreases in stomatal conductance. There is evidence to suggest that when exposed to water stress J. curcas accessions switch from C3 mode of photosynthesis to CAM photosynthetic pathway. This is attested to by the slightly low leaf pH at night. Thamaga accession exhibited an earlier stomatal closure than the other two accessions. This resulted in Thamaga accession displaying a slightly lower dry weight than both Mmadinare and Maun accessions. It could be concluded that Jatropha curcas appeared to tolerate water deficit stress due to its ability of switching from C3 photosynthetic pathway to the CAM photosynthetic pathway, but with a cost to biomass accumulation, as demonstrated by slightly more reduced CO2 assimilation by Thamaga accession, than the other two accessions.

Jatropha curcas L: Phytochemical, antimicrobial and larvicidal properties

Objective: To evaluate antimicrobial activities as well as the phytochemical and lavicidal properties of different parts of Jatropha curcas L.(J. curcas) growing in Mauritius.Methods: Determination of the presence of phytochemicals in the crude plants extracts by test tube reactions. Disc diffusion method and microdilution method were used to detect the antimicrobial sensitivity and activity(minimal inhibitory concentration). The crude solvent extracts were also tested on the larvae of two insects, Bactrocera zonata and Bactrocera cucurbitae(Diptera, Tephritidae).Results: The antimicrobial activities were significantly dependent for the different crude plant extracts on the thirteen microorganisms tested. For the Gram-positive bacteria, the crude ethyl acetate extract was more efficient compared to the Gram-negative bacteria with both solvents being effective. The crude ethyl acetate extract of J. curcas bark and mature seed oil showed the highest efficacy. The highest mortality percentage was observed after 24 h for both Diptera flies with(66.67 ± 2.89)% of Bactrocera cucurbitae larvae killed by ethyl acetate extract of J. curcas bark.Conclusions: This paper compared the different J. curcas plant sections with respect to the effectiveness of the plant as a potential candidate for new pharmaceuticals. The larvicidal effect was also studied in order to demonstrate the dual purpose of the plant.

Distribution and development strategy for Jatropha curcas L. in Yunnan Province, Southwest China

Yunnan Province is the main distributing area ofJatropha curcas L. This plant is abundant in several drainage areas of the dry-hot, dry-warm and sub-humid valleys in the south subtropical area of Yunnan Province. The seeds that were picked from trees blossoming between April and May and fructifying between September and October will have large seed yield and fine quality. For developing bio-diesel stock forest ofJ. curcas in areas with adaptive climate, seeding measures for afforestation should be taken and techniques on breeding, fast-growing, and high-yielding plantation cultivation are very important.

Floral display and breeding system of Jatropha curcas L.

Plant flowering and breeding characteristics are important for us to understand the reproduction of plant populations. In this paper, we studied the reproduction characteristics of Jatropha curcas in Yuanjiang County （23°36＇1＇4, 101°00＇E）, Yunnan Province. The plant produces flowers in dichasial inflorescences. Normally, the flowers are unisexual, and male and female flowers are produced in the same inflorescence. Only a few male flowers are produced in an inflorescence, and fruits are produced only through pollination between different flowers from the same or different plants. By the treatments of emasculation, bagging and artificial pollination in this experiment, there were few but same fruit set ratios when the inflorescences were emasculated, bagged, or bagged with net, except artificial pollination treatments, which showed that Jatropha curcas could produce fruit through apomixis but not wind pollination. When the inflorescences were unbagged, unemasculated and with free pollination treatments, or bagged, emasculated and with artificial cross-pollination treatments, or unbagged, emasculated and with free pollination treatments, there were many fruits produced. It showed that Jatropha curcas shows outcrossing, is self-compatible, and demanding for pollinators. Normally, the male flowers open first and a few flowers bloom in one day in a raceme. These flowers last a long time in bloom. However, a large number of female flowers open from the third to the fifth day, with some female flowers opening first in a few raceme. This shows a tendency to promote xenogamy and minimize geitonogamy.

Cloning and characterization of a stearoyl-ACP desaturase gene from Jatropha curcas

Using degenerate primers and RT-PCR, RACE techniques, a 1491 bp cDNA segment of stearoyl-acyl carrier protein desaturase （SAD） is cloned from developing seeds of Jatropha curcas L. The segment contains a 1191 bp of complete open reading frame （ORF）. Analysis in the BLAST on NCBI shows that Jatropha curcas SAD （JSAD） gene encodes a protein precursor composed of a signal peptide of 33 amino acids and a mature peptide of 363 amino acids. The homological analysis shows that JSAD has high level of homology both in nucleotide sequence and in amino acid sequence to other plants SADs. The nucleotide and peptide identity of JSAD to Ricinus communis SAD （RSAD） is up to 89% and 96.2% respectively. Molecular modeling of JSAD indicates that its three-dimensional structure strongly resembled the crystal structure of RSAD.

The biomedical significance of the phytochemical, proximate and mineral compositions of the leaf, stem bark and root of Jatropha curcas

Objective: To analyse the phytochemical contents of leaf, stem bark and root of Jatropha curcas(J. curcas) in four solvent extracts and their proximate and mineral compositions. Methods: Standard analytical procedures were used for the determination of phytochemicals, proximate and mineral compositions of the leaf, stem bark and root extracts of J. curcas. Results: Results of the analysis showed the presence of polyphenols, flavonoids, alkaloids, cardiac glycosides, coumarins, saponins, terpenoids, steroids, triterpenoid saponins, carotenoids, phlobatannins and tannins in the leaf, stem bark and root of all the solvent extracts. Flavonoids were present in the highest amount in the ethyl acetate extracts of the leaf(7.35% ± 0.02%), stem bark(4.12% ± 0.01%) and root(3.35% ± 0.02%) followed by polyphenols in the methanol extracts of leaf(4.62% ± 0.02%), stem bark(2.77% ± 0.05%) and root(2.49% ± 0.02%). Poly-acetylated compounds were absent in all the solvent extracts of the leaf, stem bark and root. However, some anti-nutritional agents such as oxalates, phytates and cyanates were present in all the solvent extracts of the leaf, stem bark and root except the ethyl acetate. Phytates were high in the aqueous solvent of the leaf(6.12% ± 0.00%) but low in the stem bark(1.00% ± 0.05%) and root(0.89% ± 0.03%). Proximate composition showed appreciable amounts of total carbohydrate(36.33% ± 0.72%), crude protein(26.00% ± 0.47%) and reducing sugars(5.87% ± 0.14%) in the leaf, while crude fat was more in the stem bark(16.70% ± 0.30%). There was corresponding substantial energy in the leaf [(1 514.77 ± 20.87) kJ /100 g] and stem bark [(907.00 ± 8.52) kJ /100 g]. Moisture and ash contents of the leaf, stem bark and root were within acceptable limits for the use in drugs formulation. The mineral composition showed substantial amounts of important elements such as Fe, Ca, Na, Mg and Zn. Others were P, K and Se. Conclusions: The outcome of this study suggests that the leaf, stem bark and root of J. curcas have very good medicinal potentials, meet the standard requirements for drug formulation and serve as good sources of energy and nutrients except for the presence of some anti-nutritional elements predominant in the leaf.

<i>In</i><i>Silico</i>Mining of EST-SSRs in Jatropha curcas L. towards Assessing Genetic Polymorphism and Marker Development for Selection of High Oil Yielding Clones

In recent years, Jatropha curcas L. has gained popularity as a potential biodiesel plant. The varying oil content, reported between accessions belonging to different agroclimatic zones, has necessitated the assessment of the existing genetic variability to generate reliable molecular markers for selection of high oil yielding variety. EST derived SSR markers are more useful than genomic markers as they represent the transcriptome, thus, directly linked to functional genes. The present report describes the in silico mining of the microsatellites (SSRs) using J. curcas ESTs from various tissues viz. embryo, root, leaf and seed available in the public domain of NCBI. A total of 13,513 ESTs were downloaded. From these ESTs, 7552 unigenes were obtained and 395 SSRs were generated from 377 SSR-ESTs. These EST-SSRs can be used as potential microsatellite markers for diversity analysis, MAS etc. Since the Jatropha genes carrying SSRs have been identified in this study, thus, EST-SSRs directly linked to genes will be useful for developing trait linked markers.

Potential Technological Use of Reserves of <i>Jatropha curcas</i>and <i>J. macrocarpa</i>Griseb. Seeds

J. curcas and J. macrocarpa are useful for restoring degraded areas and their seeds contain oils for biodiesel production. The aim of the work was to determine the reserve substances in the endosperm and the embryo of J. curcas and J. macrocarpa which is important in understanding the germination process, the establishment of these species and its industrial employment. Seeds were imbibed in distilled water for 24 h, to facilitate removal of seed coat with the aim to separate the embryo and nutritive tissues. In both species, the endosperm contained aleurone grains consisting of a crystalloid and globoid, lipids of red color and the starch was not observed. Four major fatty acids were determined in J. curcas seed: oleic, palmitic, stearic, palmitoleic and oleic fatty acid represents about 70% oil content. Oleic acid was the most abundant in J. macrocarpa seeds, while, there was not palmitoleic acid. Seed with predominantly unsaturated fatty acids is ideal for biodiesel industry. The means of the sugar content were: 14.3 μg/mg in endosperm and 104.76 μg/mg in embryo of J. curcas and 6.48 μg/mg in endosperm and 59.20 μg/mg in embryo of J. macrocarpa. The means of the protein content were: 4.2 μg/mg in endosperm and 45.02 μg/mg in embryo of J. curcas and 3.26 μg/mg in endosperm and 31.08 μg/mg in embryo of J. macrocarpa. Sugar and protein contents of Jatropha seeds were significantly higher in embryo in both species (p 0.1), which suggests early mobilization towards the embryo during imbibition period.

Production, Characterisation and Fatty Acid Composition of <i>Jatropha curcas</i>Biodiesel as a Viable Alternative to Conventional Diesel Fuel in Nigeria

Ethyl ester biodiesel has been produced from a non-edible Jatropha curcas oil. Oil was extracted from the plant seed using n-hexane at 60°C and pretreated by alkaline refining process to reduce the free fatty acid level to less than 1%. Base-catalysed transesterification reaction with absolute ethanol using potassium hydroxide catalyst was adopted for the conversion. Various physicochemical properties of the refined Jatropha curcas oil were investigated. The ethyl ester biodiesel produced was characterised for its fuel properties such as specific gravity at 15°C, flash point, pour point, kinematic viscosity, cetane number, iodine value and higher heating value using American Society for Testing and Materials Standard Methods. The crude and refined Jatropha curcas oil yields were 58.16% and 52.5%. The physicochemical analysis revealed FFA, saponification value and peroxide value of refined Jatropha curcas oil to be 0.58 mg KOH/g, 159.9 and 1.92 m E/kg respectively. The fatty acid composition obtained from gas chromatography (GC) revealed that the oil contained 44.85% oleic acid as the dominant fatty acid, while Margaric 0.01% and Behenic 0.02% the least. The biodiesel yield was 57.6%, and its measured fuel properties conformed with ASTM 6751 and EN 14214 standards.

Synthesis of biodiesel from Jatropha curcas L. seed oil using artificial zeolites loaded with CH3COOK as a heterogeneous catalyst

An environmentally benign process was devel-oped for the transesterification of Jatropha curcas L. seed oil with methanol using artificial zeolites loaded with potassium acetate as a heterogeneous catalyst. After calcination for 5 h at 823 K, the catalyst loaded with 47 wt.% CH3COOK exhibited the highest efficiency and best catalytic activity. The easily prepared cata-lysts were characterized by means of X-ray dif-fraction and IR spectroscopy, as well as Hammett indicator titration. The results revealed a strong dependence of catalytic activity on ba-sicity. The optimum reaction conditions for transesterification of J. curcas oil were also in-vestigated. The methyl ester content in the bio-diesel product exceeded 91% after 4h reaction at reflux temperature in the presence of 2% solid catalyst and no water washing process is needed during workup.

Development of a New Bio-Based Insulating Fluid from <i>Jatropha curcas</i>Oil for Power Transformers

The present work aims to develop a new vegetable insulating fluid for power transformers based on Jatropha curcas oil. Besides its technical benefits, Jatropha curcas oil has a socio-economic role by promoting income to rural families, contributing to the countryside development and avoiding rural exodus. Thus, the entire transformer oil production (extraction, processing, characterization and accelerated aging) was covered and a new process was developed. For oil extraction, the most suitable process was the solvent extraction (5 mL of hexane per gram of crushed non-peeled seeds during 30 minutes) with an oil yield of 32%. In raw oil processing stage, the degumming, with 0.4 g of phosphoric acid per 100 g of oil, at 70°C, was used to remove phosphatides. Then, free fatty acids were 96% neutralized with a sodium hydroxide solution (0.5% w/w) at room temperature. For the oil clarification, the combination of 5% w/woil of activated carbon and 1% w/woil of MgO resulted in a bright, odorless and clear oil with an acid number of 0.04 mgKOH·g﹣1. The oil drying in a vacuum rotary evaporator, at 70°C, for 2 hours reduced the water content to 177 ppm. The processed oil was characterized following ASTM D6871 methods. This oil presented higher dielectric breakdown voltage (55 kV) than commercial transformer fluids (BIOTEMP?, EnvirotempFR3?, and Bivolt?), which increases transformer safety, capacity and lifetime. In addition, the processed oil has a lower viscosity than BIOTEMP? fluid, which can enhance the heat dissipation efficiency in the transformer. Moreover, the processed oil flash and fire points of 310°C and >340°C, respectively, confirm the great security of vegetable insulating fluids. The analyzed properties of the processed oil fulfill all the ASTM D6871, ABNT NBR 15422 and IEC 62770 specifications. Therefore, Jatropha curcas oil is a potential substitute formineral insulating fluids.

Physicochemical Characterization of <i>Jatropha curcas</i>Linn Oil for Biodiesel Production in Nebbi and Mokono Districts in Uganda

Jatropha curcas Linn has been identified worldwide as one of the sources of biodiesel. Biodiesel has energy properties close to fossil diesel and can be a potential energy alternative. However, these properties may vary based on soils, plant genetics and agro-climatic conditions in a given geographical location. Several studies on biodiesel production under such conditions have been done elsewhere, but few have been done on J. curcas oil in Uganda. This study analysed the physicochemical properties of J. curcas L. oil for biodiesel production in Nebbi and Mukono districts using American Standards and Testing Methods (ASTM D6751) and European Standards (EN 14214). J. curcas seed kernel contained 51% w/w and 48% w/w of oil with high levels of Free Fatty Acids (1.52% and 1.93%) and acid values (35 and 36 mg KOH/g) for Nebbi and Mukono, respectively;the difference was significant (p ≤ 0.05). Generally, the quality and quantity of the oil from Nebbi were better than those of Mukono, based on the biodiesel standard values. Nevertheless, kinematic viscosity, acidity, potassium and phosphorus content values were found abnormally high (31.46 - 33.23 mm2/s, 35.23 - 36.66 mg KOH/g, 16.50 - 20.52 mg/100g and 16.13 - 26.02 mg/kg, respectively) for both regions as compared to the standard values (3.5 - 5.0 mm2/s, 2 mg KOH/g, <5 mg/100g and <10 mg/kg, respectively) of biodiesel for diesel engine. Such properties are very important for engine fuels and if not considered well, may affect engine performance negatively. Therefore adequate treatment of the oil by degumming, etherification and transesterification before use in a diesel engine could avert this difficulty.

Some Biological Features of Aphtona whitfieldi Bryant (Coleoptera: Chrysomelidae), an Insect Pest of Jatropha curcas L. in Burkina Faso

Aphthona whitfieldi Bryant (Coleoptera: Chrysomelidae) is a major insect pest of Jatropha curcas L. (Euphorbiacae) in Burkina Faso and other countries in West Africa. The insect pest feeds on the roots and the leaves of the plant. When the attacks are heavy, the plant may lose all its leaves and die off. Unfortunately, little information is available on the biology of this insect pest. A study was conducted on the biology of this insect pest in the Sissili province, South Burkina Faso and resulted in the knowledge of some of the biological features of the insect pest. Aphthona whitfieldi was reared from 13th July to 22th October 2015. Larvae and pupae were collected in J. curcas plantations near Léo, the capital city of the Sissili province, and brought to the laboratory for rearing. The insects were observed daily and the dimensions and the duration of each stage were recorded. We recorded two larval stages (1st and 3rd): a pre-pupa and a pupal stage. The pupa was free and white milk-like. Both the pre-pupa and the pupal stages lasted for five days. The 1st instar larva was smaller than the third one.

Gene cloning,expression analysis of JcACP (Acyl Carrier Protein) in Jatropha curcas L. and its prokaryotical expression

Objective To clone the ACP(acyl carrier protein)gene in Jatropha curcas L.,a potential anti-tumour and anti-fungal plant.And to determinate the expression of ACP in Jatropha curcas L.Methods A cDNA clone encoding ACP(acyl carrier protein)was isolated from Jatropha curcas L.endosperm cDNA library by random sequencing.The expression of ACP gene was investigated by semi-quantitative RT-PCR in leaves,stems and seeds of J.curca.The expression of ACP was also investigated in germinating seeds.The fragment encoding ACP protein in J.curca.was inserted into a prokaryotic expression vector pET28a(+).The gene was overexpressed in E.coli BL21 to produce abundant protein.Immunohistochemical analysis was used to detect the expression of ACP in different tissues of J.curca.Results The cDNA sequence was 806 bp in length and the ORF was 393 bp.The predicted molecular weight of the putative protein was 14.4 kD,pI=5.2.It contained a 4'-phosphopantetheine-binding motif.This prosthetic group can be combined with Serine of ACP protein.Semi-quantitative RT-PCR analysis showed that ACP gene was expressed in leaves,stems and seeds of J.curcas.The expression level of ACP was the highest in seeds and it was not detected in roots.After seeds germinated,the expression level of ACP in seeds increased progressively and reached a peak at 96 h.After induced by IPTG,SDS-PAGE analysis showed that the ACP protein of 20 kD was expressed.Immunohistochemical analysis showed that ACP specifical expressed abundantly in embyo of the seeds,and it was not detected in roots and the emdosperm while expressed in leaves and stems.Conclusions A cDNA clone encoding ACP which had all the typical characteristics of ACPs was isolated.It was expressed successfully in E.coli.The results of semi-quantitative RT-PCR analysis and immunohistochemical analysis were very similar,which showed that the expression of ACP in J.curcas.was abundant in seeds.The results indicated the expression related to the high metabolism.

Isolation of a genomic DNA for Jatropha curcas ribosome inactivating protein and its tobacco transformation

Genomic DNA for Jatropha curcas ribosome inactivating protein （JRIP） was cloned from total DNA of its leaves by polymerase chain reaction （PCR）. The no intron character was confirmed. The plant expression vector pBI121-JRIP was constructed by inserting the JRIP gene into pBI121 plasmid. The recombinant Agrobacterium EHA105 strain harboring pBI121-JRIP was constructed by conducting pBI121-JRIP to strain EHA 105. PCR and Southern blotting were carried out, and the results proved that the JRIP gene was integrated into tobacco genome. It might provide a new material for disease resistance tobacco species breeding.

New jatropholane-type diterpenes from Jatropha curcas cv.Multiflorum CY Yang

Three new jatropholane-type diterpenoids,jatropholones C-E(1-3),along with seven other known compounds,including sikkimenoid B(4),jatrophaldehyde(5),epi-jatrophaldehyde(6),epi-jatrophol(7),jatrophol(8),jatropholone A(9),and jatropholone B(10),were isolated from the roots of a natural cultivar of Jatropha curcas(J.curcas cv.Multiflorum CY Yang).The structural elucidations of 1-3 were accomplished by extensive NMR analysis.Compounds 4,6,and 8 demonstrated inhibition activity against the microorganisms with the MIC values from 0.10 to 0.18 mg/mL.

Insight of Viral Infection of Jatropha Curcas Plant(Future Fuel):A control based mathematical study

Jatropha Curcas Linnaeous(Jatropha Curcas L)is a wonder plant with a variety of applications and enormous economic potential.Biodiesel,an alternative fuel from non edible vegetable oil of Jatropha Curcas plant,has the requisite potential of providing a promising and commercially viable alternative to diesel oil since it has the desirable physicochemical and performance characteristics comparable to diesel.This alternative fuel is eco-friendly,cost effective and has the huge potentiality for the future generations throughout the world.For effective cultivation of this plant, protection from different viral diseases is essential.In this paper,we describe the eco-epidemiological model of the plant Jatropha Curcas L for understanding the disease dynamics which helps to control the viral infection of the Jatropha Curcas plant cell.By this approach,this plant can grow ideally for the renewable green fuel of the future world.

Pyrolysis Oil from the Fruit and Cake of Jatropha curcas Produced Using a Low Temperature Conversion (LTC) Process: Analysis of a Pyrolysis Oil-Diesel Blend

Background: The LTC process is a technique that consists of heating solid residues at a temperature of 380oC - 420oC in an inert atmosphere and their products are evaluated individually: these products include pyrolysis oil, pyrolytic char, gas and water. The objective of this study was to compare the effects of the use of oils obtained by pyrolysis of Jatropha curcas as an additive for diesel in different proportions. Results: A Low Temperature Conversion (LTC) process carried out on samples of Jatropha curcas fruit and generated pyrolysis oil, pyrolyic char, gas and aqueous fractions in relative amounts of 23, 37, 16 and 14% [w/w] respectively for Jatropha curcas fruit and 19, 47, 12 and 22% [w/w] respectively for Jatropha curcas cake. The oil fractions were analyzed by FTIR, 1H NMR, 13C NMR, GCMS and physicochemical analysis. The pyrolysis oil was added to final concentrations of 2, 5, 10 and 20% [w/w] to commercial diesel fuel. The density, viscosity, sulfur content and flash point of the mixtures were determined. Conclusions: The results indicated that the addition of the pyrolysis oil maintained the mixtures within the standards of the diesel directive, National Petroleum Agency (ANP no 15, of 19. 7. 2006), with the exception of the viscosity of the mixtures containing 20% pyrolysis oil.

In-Vitro Efficacy of Certain Essential Oils and Plant Extracts against Three Major Pathogens of Jatropha curcas L.

Antifungal activity of plant extracts and essential oils of six different plant species was tested against three pathogenic fungi, viz., Alternaria alternata, Colletotrichum gloeosporioides and Fusarium moniliforme isolated from Jatropha curcas L. using Poison Food Technique. All the samples tested were found effective in-vitro. More than 60% inhibition of growth of individual fungal species was observed at 100 ppm. Maximum inhibition was observed at concentration of 1000 ppm. However, among the essential oils tested Cinnamomum impressinervium exhibited the strongest activity (80%) in the case of Colletotrichum gloeosporioides and Alternaria alternate and 78.6% in the case of Fusarium oxysporum at concentration of 1000 ppm followed by Cinnamomum tamala, Cymbopogon jwarancusa and Cymbopogon citratus respectively. Among the plant extracts tested, Catharanthus roseus exhibited stronger activity in comparison to Tithonia diversifolia. Inhibition percentage of all the essential oils and plant extracts increased with the increase in concentration.