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Ectopic Overexpression of Lectin in Transgenic Brassica juncea Plants Exhibit Resistance to Fungal Phytopathogen and Showed Alleviation to Salt and Drought Stress
ISSN: 2155-9538
Journal of Bioengineering & Biomedical Science

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Ectopic Overexpression of Lectin in Transgenic Brassica juncea Plants Exhibit Resistance to Fungal Phytopathogen and Showed Alleviation to Salt and Drought Stress

Deepak Kuma1, Shashi Shekha1, Sandip Bisht2, Vivek Kumar3, Ajit Varma3, Manoj Kumar3* and Mukesh Saxena4

1School of Life Sciences, Jawaharlal Nehru University, New Delhi-110067, India

2Department of Molecular Biology and Biotechnology, VCSG college of Horticulture, Uttarakhand University of Horticulture and Forestry, Pauri-246123, Uttarakhand, India

3Amity Institute of Microbial Technology, Amity University Uttar Pradesh, Noida-201303, India

4Monsanto Research Centre, Bengaluru, Karnataka 560045, India

*Corresponding Author:
Manoj Kumar
Amity Institute of Microbial Technology
Amity University Uttar Pradesh
Noida-201303, India
Tel: +91-120-4392432
E-mail: [email protected]

Received Date: March 16, 2015; Accepted Date: March 24, 2015; Published Date: March 31, 2015

Citation: Kuma D, Shekha S, Bisht S, Kumar V, Varma A (2015) Ectopic Overexpression of Lectin in Transgenic Brassica juncea Plants Exhibit Resistance to Fungal Phytopathogen and Showed Alleviation to Salt and Drought Stress. J Bioengineer & Biomedical Sci 5:147. doi:10.4172/2155-9538.1000147

Copyright: ©2015 Kuma D, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Lectins are ubiquitous in nature and one of the most important secondary metabolites in plants. They are heterogeneous class of proteins that bind specifically and reversibly to carbohydrates and are used as a defence tool against various abiotic and biotic stresses. In this study, we describe generation of transgenic Brassica juncea plants over-expressing chickpea lectin in conferring fungal resistance. In addition, the transgenic plants also showed resistance against salinity (NaCl) and mannitol induced drought stress. The stable integration and transcript expression of the transgene was confirmed by southern blot and RT-PCR analysis in the transgenic plants. The transgenic lines were evaluated for resistance against Alternaria brassicae as assessed by the number and size of lesions and time taken for leaf necrosis, the Alternaria infection was delayed and restricted in the transgenic plants with the protection varying from 36-60% in different transgenic lines compared to the Untransformed Control (UC) plants. In addition, the transgenic Brassica juncea plants also showed tolerance against high salinity and drought stress. The Expression of lectin gene imparts greater water retention capacity, higher proline content and more chlorophyll retention with less membrane damage and reduction in electrolyte leakage in the transgenic plants compared to UC. Together, these findings suggest the potential use of chickpea lectin gene to engineer the crop plants for broad spectrum biotic and abiotic stress tolerance to improve crop productivity.


Abiotic stress; Alternaria leaf spot; Brassica juncea; Lectin; Transgenic


Agricultural plants face constant state of war against an array of pathogens and adverse environmental factors which are major causes in limiting crop production and have been responsible for scripting some of the most devastating famines in the human history. Brassica juncea belongs to the Cruciferae family and it is an important oil seed crop grown in many countries around the world. The oil obtained from the seeds is the main cooking medium in different parts of the world, especially in the Indian sub-continent. Brassica is also a high biomass crop and may facilitate phytoremediation of heavy metals in polluted soils [1]. In India, mustard contributes 28.6% to the total oilseed production and has been projected to provide for 41% (14 million tons) of the country’s demand by the year 2020 [2]. Due to increased demand for edible oil and biofuels, the cultivation of oilseeds crops has gained significant importance [3]. Unfortunately, the productivity of this crop has been hampered by several biotic and abiotic factors [4]. Among biotic stress one of the major constraints affecting the productivity of mustard is the Alternaria leaf spot disease caused by Alternaria brassicae [5]. However, the crop is also severely affected by abiotic stresses resulting in significant loss in seed yield. Conventional breeding approaches to develop the resistant cultivars is confounded due to non availability of suitable resistance sources within the available germplasm of cultivated and wild species of Brassica. Therefore, better combat strategies relying on generation of transgenic plants armored with defense proteins are being explored [6].

The plants have inherent defence mechanisms and an innate immune system to protect themselves against a wide range of pathogens by the discrimination between self and non-self through pathogenassociated molecular patterns [7]. The preformed physical and chemical barrier constitutively produced antimicrobial compounds which protects the plants against biotic and abiotic stress. The proteins embedded in the cell wall and plasma membrane is also an important sentinel of the system for the recognition and transduction of defense associated signals [8]. The susceptibility of plants to the pathogens is resulted due to the disruption of cell wall-plasma membrane adhesion during pathogen penetration into host cells, causes reduction in cell wall-associated defense responses, thereby making the plant more susceptible to disease [9].

Lectins are the ubiquitous carbohydrate binding proteins possess at least one non-catalytic domain that specifically and reversibly bind to mono or oligosaccharide structures and mediate different biological processes [10]. Plants lectins is also believed to be tool in the specific protein-carbohydrate interactions within the cytoplasmic and nuclear compartments [11] and to the glycoproteins present on the cell surfaces [12]. Lectin shows high affinity binding with the carbohydrate moiety of glycoproteins, glycolipids, polysaccharides and typical carbohydrate constituent of fungal cell walls [13]. Expression of Gastrodia elata lectins resulted into strong induction of Trichoderma viride, which indiates that lectin is an important defence protein in plants [14]. By the incorporation of the precursor gene of stinging nettle isolectin I into tobacco, the spore germination of Botrytis cinerea, Colletotrichum lindemuthianum, and T. viride was significantly reduced [15]. Several other plant lectins are also reported for their crucial role in the defense against phytopathogenic infection such as the potato lectin immobilizes avirulent strains of Pseudomonas solanacearum on the plant cell wall; however, avirulent strain is not recognized by lectins [16]. Hevein, a type of lectin produced by rubber tree latex shows in vitro antifungal activity against Botrytis cinarae, Fusarium oxysporum, and Fusarium culmorum [17] and also confers the protection against Alternaria leaf spot in Indian mustard [18]. Different plant lectins show their differential expression under abiotic stress including drought, salinity and temperature shock [18-22] in the different crop plants.

In view of the diversity in the protective action of lectin, we assessed the efficacy of the chickpea lectin gene, which was involved in the suppression of Alternaria leaf spot in Brassica juncea during the fungal infection. As well as the transgenic plants containing chickpea lectin showed enhancement in the tolerance to salinity and drought stress in comparison to UC plants. Collectively, the results of our study demonstrated the current efforts to generate broad spectrum of transgenic plants resistance to fungal phytopathogens along with abiotic stresses.

Materials and Methods

Plant material

The seeds of Brassica juncea cv. Varuna were taken from Indian Agricultural Research Institute, New Delhi-12.

Bacterial strain and plasmid

The chickpea letin cloned at the EcoRI - XbaI site in the pRT101 vector in between CaMV 35S promoter and polyA terminator sequences. This promoter- lectin cDNA- terminator cassette was released from pRT101 vector by digestion with HindIII and cloned at the HindIII site in the multiple cloning site of pCAMBIA 1301 (pC1301) vector to give rise to pCAM-lectin. pC1301 has hygromycin as plant selection marker and kanamycin as bacterial selection marker. This construct was confirmed by restriction digestion with HindIII as well as by PCR amplification of lectin sequence by using specific primers. Further the gene construct was mobilized into Agrobacterium tumefaciens strain GV 3101 by heat and thaw method. Agrobacterium culture was maintained on solid YEB medium and selected with 50 mgl-1 kanamycin and 100 mgl-1 each of rifampicin and carbenicillin.

Transformation, selection and plant regeneration

The construct , pCAM-lectin, was mobilized into Agrobacterium tumefaciens strain GV 3101, which was subsequently used to transform hypocotyls explants from 5 day old seedlings of Brassica juncea (cv. Varuna) . The explants were further plated on the selection medium, MSB1 N1 (MS medium supplemented with 1 mgl-1 each of 6-benzylaminopurine and α-naphthaleneacetic acid) containing AgNO3 (3.4 mgl-1) and hygromycin (30 mgl-1). The plates with explants were kept in culture room maintained at 22 ± 2ºC and 14 h: 10 h (light: dark) photoperiod. The shoots obtained after 15–20 days were subcultured on the rooting medium MSI2 (MS medium supplemented with 2 mgl-1 Indole-3- butyric acid). The established untransformed control (UC) and putative transgenic plantlets were transferred to glass house to hardened and to grow under 25 ± 2ºC temperature under 14 h:10 h (light: dark) photoperiod, with 70% relative humidity.

DNA extraction and PCR Analysis of the Transgenic Plants

Genomic DNA was extracted from the leaves of UC and transgenic (TR) plants following the protocol of [23]. The primary screening for the selection of putative transformants was performed by polymerase chain reaction (PCR) analysis using the lectin gene specific primers mentioned below: The primer set were designed from conserved region of lectin gene



The PCR reaction was carried out with Taq DNA polymerase enzyme mix along with supplied Taq buffer. The Mg2+ concentration was 1.5 mM in 50 μl reaction volume. PCR conditions were 35 cycles of 1 min at 94°C, 1 min at 55°C, and 1 min at 72°C, using 1 μg/μl of the isolated DNA as template and 10 pmol of each primer in a 50-μl reaction. At the end of 35 cycles, the reactions were incubated at 72°C for 10 min and the tubes were kept at 4°C. An aliquot of the PCR product was electrophoresed on a 1.2% agarose gel and visualized by ethidium bromide staining on UV Trans-illuminator.

Southern blot analysis

Ten micrograms of genomic DNA from UC and TR plants was digested with PstI restriction endonuclease, electrophoresed on a 0.8% agarose gel and transferred to a Hybond-Nylon membrane (Amersham Biosciences, UK) using the capillary transfer method. The membrane was prehybridized for 2 h at 65ºC in a buffer containing 0.5 M sodium phosphate buffer, pH 7.2, 1 mM EDTA, and 7% SDS. Thereafter the denatured radiolabeled probe (834 bp Lectin amplicon obtained by PCR amplification of lectin gene) labelled with [a-32P] dCTP using Random primer DNA labeling kit (Amersham Biosciences, UK) as per the manufacturer’s instructions) was added to the prehybridization buffer and incubated overnight at 65ºC. The membrane was washed (10 min per wash) sequentially in 39 SSC, 0.1% SDS; 0.59 SSC, 0.1% SDS; 0.29 SSC; 0.1% SDS with constant agitation at 65ºC. The hybridization signals were captured using phosphorimaging (FLA 5000 imaging system, Fujiflim).

In Vivo plant bioassay for resistance to fungal phytopathogen

The assessment of antifungal activity of lectin the UC and TR plants were assessed. Alternaria brassicae (Accession No. ITCC 5097) procured from the Division of Plant Pathology, Indian Agricultural Research Institute, New Delhi. The fungal culture was multiplied on potato dextrose agar (PDA) medium at 22 ± 1ºC for the maintenance. The spore suspension was prepared as explained by [24]. The spore suspension was filtered through cheesecloth to remove the mycelia debris. The spores were washed with sterile distilled water and resuspended to a count of 103 spores ml-1. For in vivo plant bioassay, the fourth leaf (from the top) of the 45-day-old UC and TR plants were painted with the spore suspension using a painting brush. The inoculated plants were covered with polybag to maintain the humidity which was conducive to infection. To assess the disease severity the development of necrotic lesions in terms of number and area on the inoculated leaf of UC and TR plants were observed and recorded up to 15 days of inoculation. Percentage disease protection was calculated by [6].

Disease protection (%) = {(No: of lesions per leaf in UC plant- No. of lesions per leaf in TR plants)}/{(No: of lesions per leaf in UC plant)}×100

Stress tolerance experiments

For drought and salt stress treatments 6-day-old seedlings of UC plantlets grown on MS plates and TR lines grown on MS plates supplemented with 30 mgl-1 hygromycin were transferred into pots containing agropeat in a growth chamber at 25ºC, 60% relative humidity, and 16 h: 8 h (Light:dark) photoperiod. To assess the drought and saline stress the UC and TR plants were irrigated biweekly with 300 mM mannitol and 300 mM NaCl solution respectively followed by rewatered for 6 days to recovery. These plants were used for performing different experiments.

Leaf disc senescence assay

To analyse the preliminary stress responses the leaf disc senescence assay was performed. For leaf disc senescence assay, leaf sections of equal diameter were excised from the fourth leaf from top of UC and TR B. juncea plants and floated on liquid MS basal medium containing NaCl (200–600 mM) or Mannitol (200–600 mM). Chlorophyll content in the leaf sections was estimated after 5 days according to the procedure of [25].

Measurement of electrolyte leakage

The Electrolyte leakage was determined according to the method described by [26]. Leaves from UC and TR plants were harvested and washed with deionized water for three times to remove surfaced electrolytes. Further they were immersed to the 10 ml of deionized water in the test tubes to measure the electrical conductivity (EC1). After incubation for 30 min at 55ºC again EC2 was determined. The samples were heated for 1 h in boiling water before the total conductivity was measured in the solution (EC3). Relative ion leakage was expressed as a percentage of the total conductivity:

Relative Electrolyte Leakage = {(EC2-EC1)/EC3]×100

Measurement of MDA content

The protocol of Heath and Packer was used to measure MDA content [27]. 1 gm of leaves of UC and TR plants were grinded to fine powder in liquid nitrogen. 3 ml of 10% trichloroacetic acid was added to 0.2 g of the homogenized powder and left at 4ºC for overnight. Further the homozenized powder was centrifuged at 1,000×g for 20 min and supernatant was transferred to a new tube. 2 ml of 0.6% thiobarbituric acid (TBA) was added to 2 ml of the supernatant. The mixture was vortexed thoroughly and heated in boiling water bath for 15 min, cooled immediately and centrifuged. The Absorbance was taken at 532 and 450 nm by using water as blank. The formula for the calculation of MDA content was: MDA content was:

(μmoll-1) = 6:45×OD532×0:56×OD450

Measurement of relative water content (RWC)

To determine the RWC, fresh leaves were detached from the UC and TR plants and weighed their fresh weight followed by dipping them in distilled water for 12 h. The leaves were blotted to wipe off excess water and weighed to record turgid weight (TW). Further leaves were placed at 70ºC for 24 h to record the dry weight (DW). The RWC was determined by the equation:

RWC = (FW- DW)×100/(TW–DW).

Estimation of proline

Proline content was estimated using the standard protocol [28]. 100 mg of leaf tissue from UC and TR plants were homogenized in 10 ml of 3% sulfosalicylic acid. The homogenate was centrifuged at 15,000 rpm. 2 ml of the supernatant was mixed with 2 ml of 0.2% ninhydrin and 2 ml of glacial acetic acid. Further the mixture was incubated at 100ºC for 1 h and the reaction was terminated on ice. Extraction of Proline was done by 4 ml of toluene. The OD of the supernatant was measured at 520 nm and proline concentration was determined from the standard curve made by using the purified L-proline (Sigma, MO, USA) and calculated on a FW basis (μmolg-1).


Generation and molecular characterization of transgenic B. juncea expressing chickpea lectin gene

Generetaion of transgenic B. juncea harbouring chickpea lectin gene was achieved by Agrobacterium mediated genetic transformation. The plasmid, pCAMBIA1301, contains chickpea lectin gene cloned between HindIII restriction site with CaMV 35S constitutive promoter with NOS termination sequence (Figure 1a). The hygromycin phosphotransferase (hpt) gene present in the plasmid was used for putative transformants selection. Preliminary screening for the transgenic B. juncea plants, selected on hygromycin was done by PCR amplification of the chickpea lectin gene. In the six independent transgenic lines, an amplicon of 834 bp was found with the chickpea lectin gene specific primer (Figure 1b). These fragments were not amplified in the UC plants. The six PCR positive TR lines produced southern positive bands with single (L1, L3, L5, L6) and double copy (L2, L4) of the transgene after the restriction digestion with PstI (Figure 1c). To check the expression level of the chickpea lectin gene in the southern positive transgenic lines, RT-PCR analysis was performed followed by the densitometrically normalizing the actin levels. Figure 1d shows the presence of 834 bp band corresponding to the amplified lectin cDNA in all the confirmed TR lines. All the transgenic plants were morphologically similar to the UC plants and showed no visible signs of impaired growth or physiology. Further these TR lines as well as the UC plants were used for the abiotic stress tolerance assay and in vivo anti fungal assay against the A. brassicae.


Figure 1a


Figure 1b: Transformation and molecular analysis of Brassica juncea plants expressing lectin gene. (b) PCR analysis to screen the transgenic plants for the presence of transgene was done using lectin gene specific primers.


Figure 1c: Transformation and molecular analysis of Brassica juncea plants expressing lectin gene. (c) Southern blot analysis of the transgenic plants showing the integration and copy number of the transgene after digestion of genomic DNA with PstI.


Figure 1d: Transformation and molecular analysis of Brassica juncea plants expressing lectin gene.. (d) RT-PCR analysis confirming expression of lectin in young fully expanded leaves of transgenic Brassica juncea plants. Actin gene was used as an internal control.

In vivo biotic stress assay

The resistant/tolerant efficiency of the candidate gene against the Alternaria leaf spot disaese was determined by In vivo plant bioassay, under controlled environmental condition. In the aforesaid protocol (Material and methods) the leaves of UC and the TR lines were inoculated with fungal spores. Further the initiation and progression of the disease lesions were analyzed in the subsequent days. After 15 days, the number of characteristic lesions on the leaves of transgenic plants was less (<9 lesions/leaf) in comparison to the leaves of the UC plants (>14 lesions/leaf) (Table 1). The size of the lesions ranged between 0.6 to 1.4 cm in diameter in the UC plants as against 0.2 to 1.0 cm in the different TR lines (Table 1). In the UC plants, the concentric rings of lesions were increasing in size until they merged with each other, which resulted into covering of whole lamina by the enlarged necrotic zone and the entire leaf dried up within 30 days of inoculation. The process of the spread of infection took more than 42 days in the case of TR plants. The percentage disease protection in the different TR lines compared with the UC plants varied between 36.6 to 60.6% (Table 1).

Plants Number of lesions (Avg ± SD) Diameter range of spots (cm) Disease protection (% ± SD)
UC 14.0 ± 1.3 0.6-1.4
L1 5.6 ± 1.0 0.3-0.6 57.9 ± 3.6
L2 5.8 ± 0.9 0.3-0.7 56.5 ± 3.9
L3 8.4 ± 0.8 0.4-0.9 38.6 ± 3.5
L4 8.7 ± 1.3 0.2-1.0 36.5 ± 5.3
L5 5.2 ± 0.7 0.2-0.5 60.6 ± 6.4
L6 6.1 ± 1.1 0.3-0.8 54.4 ± 5.2

Table 1: Evaluation of Alternaria brassicae infection on B. juncea after 15 days of inoculation. Number of fungal lesions and the diameter range of lesions were determined. The percentage disease protection in the transgenic plants with respect to the Untransformed Control plants was determined as described in materials and methods. The data presented is the average ± SD of three replicate experiments.

Transgenic plants over-expressing lectin showed higher chlorophyll retention, relative water content and proline accumulation with less membrane damage and electrolyte leakage under salt and drought stress

To investigate the effect of salt and drought stress at whole plant level, one month old plants of UCand the TR plants were transferred to the glass house in pots. To assess the effect of lectin expression on the salt and drought tolerance in transformed B. juncea. The one-monthold UC and TR plants were irrigated with 200 mM NaCl solution to induce salt stress and 200 mM of mannitol solution to induce drought stress for 3 weeks and the performance of the UC and TR plants transgenic B. juncea plants were assessed by comparing few parameters that serves as important abiotic stress markers for the tolerance of the plants.

Primarily the leaf disc senescence assay was performed to assess the ameliorative effects of lectin over-expression on leaf senescence and loss of chlorophyll due to salinity and drought stress (Figure 2a). There was loss of chlorophyll in UC plants leaf discs due to bleaching as compared to the transgenic plants leaf discs under high salt (200–600 mM NaCl) and Mannitol (200–600 mM) treatments (P ≥ 0.05). Where the UC leaf discs showed 86 and 69% decline in total chlorophyll content due to 600 mM NaCl and 600 mM Mannitol treatments respectively. The% decreases of chlorophyll content in the TR lines L1 and L5 were 57 and 62% due to imposition of salt stress, whereas 34 and 41% reduction in chlorophyll content was observed due to mannitol induced drought stress in the leaf discs excised from the L1 and L5 lines of transgenic plants respectively (Figure 2b).


Figure 2: Leaf disc senescence under stress as measured by chlorophyll content. Chlorophyll content (μg/g fresh weight) of leaf discs from Untransformed Control (UC) and transgenic (line L1 and L5) Brassica juncea plants, kept for four days at different concentrations of NaCl (panel a), mannitol (panel b). The values are means ± SE from three independent experiments. The photographs of UC and transgenic leaf discs under the corresponding treatments are presented below each plot.

Relative tolerance of UC and TR plants to the salinity and drought stresses was also assessed by comparing the electrolyte leakage from the leaf tissues of UC and transgenic plants. Under the normal condition the percentage of electrolyte leakage in the UC and TR plants has not been showed significant difference. However, percentage electrolyte leakage increased up to 71.7% in the UC plants as against an increase to 55.5 and 52.2% in the TR lines L1 and L5 respectively. The percentage of electrolyte leakage in the UC plants under mannitol induced drought stress was up to 66.1% whereas the elevation in the electrolytic leakage was 48.7 and 41.6% respectively in the L1 and L5 TR lines as compared to the UC plants (Figure 3a).


Figure 3: Comparison of abiotic stress tolerance of transgenic expressing lectin gene and Untransformed Control (UC) Brassica juncea plants. (a) Changes in electrolyte leakage from Brassica juncea leaf tissue as a percentage of total electrolytes in the leaves (b) MDA content (c) Proline content and (d) Relative Water Content (RWC) content in UC and transgenic plants exposed to NaCl (200 mM) or mannitol (200 mM) stress. The plants irrigated with water served as the untreated control. Values are mean ±SD of three experiments (three replicates per experiment). Results are significant at P<0.05.

The membrane damage due to the lipid peroxidation can be assessed by monitoring the formation of (Thiobarbituric acid reactive substances) TBARS due to the decomposition of the polyunsaturated fatty acids (PUFAs), main components of membrane lipids. We measured cellular TBARS concentration as one of the first consequences of oxidative stress, and also as an indicator of cellular damage. The MDA content in the UC and transgenic lines did not change significantly prior to the stress treatments. However, there was a significant increase in the MDA content in the UC plants compared to TR lines under salt and drought stress. UC plants showed 1.68 and1.80 fold increment in the accumulation of MDA under salinity stress, whereas the fold increase in MDA accumulation due to drought stress in the UC plants were 1.63 and 1.68 as compared to the TR lines L1 and L5 respectively (Figure 3b).

During this study the proline content was also measured under the salinity and drought stress conditions. The TR lines L1 and L5 showed 3.2 and 3.4 times more proline accumulation respectively in comparison to the UC plants under saline stress, whereas the mannitol induced drought condition resulted into the 3.4 and 3.6 times higher proline accumulation in the TR lines L1 and L5 respectively in compared to UC plants (Figure 3c).

RWC is a parameter often used to assess the water retention capacity of plants. We assayed RWC in both UC and TR plants under non-stress and stress conditions. The RWC of UC plants was comparatively less as compared to the TR plants under drought and salt stress conditions. The RWC in leaf tissues of UC plants was reduced from 90% under nonstress to 48% and 56% in salt and drought stress conditions respectively whereas the decrease in RWC in the TR plants was from a control value of 90 and 91% (in lines L1 and L5) to 74% and 76% under salt stress and 71% and 74% under drought stress respectively (Figure 3d).


The present study describes the introduction and expression of chickpea Lectin gene from into a widely grown cultivar of Indian mustard. The stringently transgenic plants were analysed through Southern blot analysis, which demonstrated that the transgenic lines were mostly containing a single copy of the transgene. The differential transcript expression profile of lectin observed between the different transgenic plants may be due to position effects of the transgene integration as the transgenes has integrated at different sites on the plant genome [29]. It is therefore, mostly desired to have single copy of candidate gene in transgenic lines.

Yield losses due to different abiotic and biotic stress are a serious problem in the cultivation of this crop [6]. The antifungal role of plant lectins due to their affinities to the carbohydrate are well documented in the scientific findings against several plant fungal phytopathogens [17,18]. The number and the size of lesions are important determiners for the degree of resistance to the leaf blight disease in Brassica species [24]. In the present study the severity of disease in the terms of number and area of lesion were assessed. Fewer numbers of lesions were recorded on the leaves of TR lines as compared to the UC plants after the fungal infection caused by A. brassicae. Further the expansion rate of lesions was higher in the UC plants with respect to the transgenic lines. Srivastava and Srivastava reported that A. brassicae produces polygalacturonase and cellulases to degrade the cell wall of host plants [30]. It is well documented fact of research findings about the high avidity binding of lectins with the carbohydrate ligands present on the microbial surfaces . This high avidity binding causes the activation of opsonisation processes by the lectins by which the lectins interact with the phagocytic cells membrane receptors which lead to the stimulation of immune response [31]. In view of the above findings, it can be conclude that, due to the interaction between the lectin and carbohydrates moiety on the fungal wall which resulted into the hypersensitive responses which leads to the restriction of new lesion formation as well as the lesion area expansion on the leaves of transgenic plants compared to the UC plants. Reduction in the number and area of necrotic lesions are important marker of disease resistance in case of fungal infection in plant species. Rustagi et al. also reported that declination in the number and area of lesions caused by A. brassicae by over-expression a synthetic antimicrobial peptide in transgenic B. juncea [32].

Production of reactive oxygen species (ROS) is one of important manifestation of the abiotic and biotic stress conditions. To minimize the ameliorative effect of the ROS toxic metabolite, the plant produces different non-enzymatic effecter molecules. Relative tolerance of UC and TR plants to these stresses was assessed by measuring different parameters viz., electrolyte leakage, RWC, accumulation of MDA and proline [33]. Maintenance of high water content is an important marker of stress tolerance in plants. The results of the present study showed that RWC in TR lines L1 and L5 maintained at significant higher levels as compared to UC plants where it is decline due to imposed stress conditions. Bhushan et al. reported that lectin was expressed under stress condition and may be involved in the stabilization of the cytoskeleton structure under stress conditions [34]. Coefficient of lectin activity was increased by 2-15 times during the high temperature, osmotic and salinity stress in oil seed flax. The development of resistance by plants against abiotic stresses depends on the location of lectins in cell organelles. During the adaptation to stress the specificity of cytosolic and vacuolar lectins for carbohydrate are changed, such as total soluble lectin exhibit capacity to binding mannose and xylose, to saline stress galactose, glucose, and glucosamine. The candidate gene chickpea lectin was cloned under the CaMV 35S promoter which constitutively expresses the lectin which was evident with the differential transcript expression. The constitutive expression of lectin may be responsible for maintenance of the cellular pool of lectin which could be regarded as the suppressor of the stress response by direct participation with modification in their quantitative and qualitative characteristics. Moreover it can be suggested that, the lectins may be regarded as drivers for plants to adapt various abiotic stresses. The increased electrolyte leakage under stress conditions in case of UC plants suggested much severe membrane damage compared to TR lines. The difference in the membrane damage was also evident in the higher MDA content in UC in comparison to TR lines. MDA accumulates as a result of lipid peroxidation, which is an effective indicator of oxidative damage. Our analyses also shows that lectin genes have been involved in biotic/abiotic stress regulations and tandem/ segmental duplications may be regarded as drivers for plants to adapt various environmental stresses through duplication followed by expression divergence.

In conclusion, our work demonstrates the generation of an economically important oilseed crop having spectrum resistance against fungal pathogens by transgenic expression of an antimicrobial peptide. This could be potentially reduce the yield loss caused by the salinity, drought and Alternaria leaf blight disease with decrease the degree of the dependence on fungicides that are increasingly being wished-off on the perspective of environmental, health, and economical reasons.


The authors are thankful to the Defence Research Development Organization (Project No.TC/2519/INM/-04/2012/CARS of INM1.2/311), Govt. of India for the partial financial support. The authors (particularly Manoj Kumar, Ajit Varma and Vivek Kumar) are thankful to Amity University, Noida and Lovely Professional University for facility and other administrative support.


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