American Journal of Plant Sciences
Vol.09 No.13(2018), Article ID:89447,18 pages

DNA Barcoding and Identification of Medicinal Plants in the Kingdom of Bahrain

Malabika Roy Pathak1*, Abdulaziz A. M. Mohamed1,2, Muhammad Farooq1

1Department of Life Sciences, Arabian Gulf University, Manama, Kingdom of Bahrain

2Ministry of Works and Municipalities Affairs and Urban Planning, Manama, Kingdom of Bahrain

Copyright © 2018 by authors and Scientific Research Publishing Inc.

This work is licensed under the Creative Commons Attribution-NonCommercial International License (CC BY-NC 4.0).

Received: November 5, 2018; Accepted: December 23, 2018; Published: December 26, 2018


Authentication of medicinally important plants is essential for increasingly demands of herbal remedies worldwide. DNA barcoding technology is currently gaining importance as a reliable tool for plant species identification, although one barcode gene is not enough in the exceptions. Short sequence diversity of standardized specific coding gene regions of rbcLa and matK of plastid genome together with noncoding ribosomal internal transcribed spacer 2 (ITS2) marker is used as barcode to compare and differentiate plant species. The success of obtaining sequences of the 29 analyzed plants distributed in 21 families using three different barcode genes rbcLa, matK and ITS2 were 97%, 79% and 75% respectively. Multiple sequence alignment confirmed the medicinal plants at species level by 89.28%, 86.32% and 60.86% obtained through rbcLa, ITS2 and matK barcodes sequences respectively. The genetic distance between sequence pairs (GD) and percentage identity (PI) is compared to analyze the plant identity at species level. The phylogenic trees constructed to show the relatedness and distance of the analyzed plants in the history of evolution by the analysis of richness of clades. The construction of DNA barcode library of desert medicinal plants is an introductory research arena in Kingdom of Bahrain in helping the routine identification of plants, and developing guidelines for detection of adulterants in herbal medicines as well as protection of biodiversity.


DNA Barcode, Medicinal Plants, Phylogenetic Tree, Species Identification

1. Introduction

Medicinal plants are used since ancient time for the treatment and management of human and animal diseases. The use of medicinal plants in traditional medicine as well as in modern drugs discovery has well documented to maintain world health and to treat chronic diseases [1] [2] [3]. According to WHO, in an estimation around 25% modern drugs are derived from medicinal plants either directly or indirectly and between 70% - 95% of the populations of developing countries and 42% - 80% population of developed countries including the USA and Europe, using traditional medicines as primary health care in different name according to regions [4]. Drug discovery from medicinal plant leads to various target diseases including cancer, HIV/AIDS, Alzheimer’s, malaria, and pains etc. and around 60% of the antitumor and anticancer drugs have derived from natural products [5] [6]. Although, drug discovery of medicinal plants explored only a small fraction of the huge diversity of plant metabolism, while most of the secondary bi-products have huge contributions in human society [7].

The Kingdom of Bahrain, geographically consists of several scattered islands in the middle of the Arabian Gulf, prevails semi-desert to desert environment with year wide average day temperature 36˚C (14˚C to 48˚C), scanty of average rainfall (39 to 128 mm per year) and holds several hundred species of flora. The number of vascular plant species reaches 357 of which most of these plants are adapted to the hot, arid and semi-arid environment [8]. Among them, 25% plants are used as a medicinal herb by Bahrainis or by others residents in the Arabian Peninsula or neighboring countries [9]. The usefulness of regional plants around 70% is of native while others introduced through Bedouin culture of the Arab region. The practice is still strong in the rural Arab regions in the treatment of minor ailments with these plants including ulcers, pneumonia, stomach disorders, rheumatism, diabetes, renal problems, and bronchitis [10] [11]. Some of the medicinally important desert plants are multipurpose plants in the Kingdom of Bahrain and some of them are threatened and restricted in distribution due to rapid urbanization, climate change as well as unsustainable utilization of natural resources [12] [13].

In the recent time, the correct identification of medicinal plants is prerequisite for their safe use in new drug discovery. The traditional identification of plants by taxonomist needs collection of proper morphological data during their growing season with reproductive organs such as flowers and fruits, which are often difficult, time consuming, and mostly unavailable during field survey [14] [15]. Moreover, the traditional methods of using the medicinal plant to cure various diseases is common but due to lack of proper taxonomic identification, the herbal industry suffers for substitution and adulteration of medicinal herbs with closely related species [16]. Identification of biological samples using DNA barcoding is a novel method of species identification and study molecular evolution [15]. DNA barcoding is considered as a molecular and bioinformatics tool for species differentiation, identification and discovery of new species at molecular taxonomy level [17]. DNA barcodes are short, specific regions of DNA that can amplify and can be sequenced routinely using universal primers and the recovered standardized short sequence of DNA depicted as a unique identification marker for species [18]. Gradually, study and comparison of unknown plant barcode sequences with the sequences of the Global DNA reference libraries help to identify unknown plant samples as well as helpful to evaluate, understand, preserve and utilize biodiversity in a widely presented way [19].

The searching of DNA barcode in a wide range of flowering land plants is delicate as well as challenging enough in comparison to animal barcode region of mitochondrial gene COI, which is not effective in plants [20]. Hybridization, lack of sequence polymorphism, low nucleotide substitution rate and frequent integration of gene flow between sister species are the critical barriers in the selection of universal barcoding gene region in land plants [17]. Moreover, the desert plants adopted to endure in tough conditions of environment and soil; as a result, they possess different survival characteristics and molecular diversity [21]. The success in identification of plant species based on DNA barcode analysis depends on the comprehensive database analysis, otherwise missing and cryptic species cannot be identified, if identified there is a risk of the tested sample to a wrong species [22]. In addition, the presence of shared haplotype between closely related species (having identical DNA sequences) is facing limitations of the technique [18]. Barcoding of vascular plants was mostly focused on markers of chloroplast genes, several markers were tested and with time most commonly used combinations are rbcL, matK, trnH-psbA, with a nuclear internal transcribed spacer (ITS2) established [18] [19] [23] [24].

The survival characteristics of the desert medicinal plants due to the harsh arid environment as well as the archipelago nature (natural as well as artificial) of the Kingdom of Bahrain restricted plant distribution over the time of urbanization [10]. Until recently, there is no report to work on DNA barcode of any plants in Kingdom of Bahrain for identification or any other purpose. We collected 29 medicinally important plant species of Kingdom of Bahrain from different location. The sampling purpose is the molecular identification of collected 29 medicinally important plant using DNA based barcode study. Here, our primary goal is development, comparison and selection of the best DNA barcode marker of the desert medicinal plants in the Kingdom of Bahrain using universally accepted marker genes rbcLa, matK and ITS2. Moreover, we want to evaluate the taxonomic authentication of species by the barcode sequence analysis. The comparison of barcode DNA sequences of the local medicinally important plant at the genus or species level is based on basic local alignment search tool (BLAST) and global multiple sequence alignment (MSA) using GenBank accessions. The evaluation of sequences of the three different markers for the identification of the desert medicinal plant is helpful to choose the effective marker for future study. We also studied the barcode gap of the analyzed plants at interspecific to investigate phylogenetic relationship. DNA barcode library of desert medicinal plants in the Kingdom of Bahrain is an introductory and important research arena in Kingdom of Bahrain. Additionally, the DNA barcode sequences of desert medicinal plants in the global sequence library (GenBank) would be useful for plant identification nationally as well as globally.

2. Materials and Methods

2.1. Study Area

Collection of local medicinal plants of Kingdom of Bahrain covered eight different regions as shown in Figure 1.

2.2. Plant Collection, Voucher Preparation and Identification

Plant samples were collected during their vegetative and reproductive growth stage in the two successive year 2016-2017 (January 2016 to April 2016, December 2016-April 2017) by several field trips in the different area, as the most of the annual desert plants, start growing after winter rainfall and perennial plants enter reproductive phase. Following the methodology of Barcode of Life Database (BOLD), whole plants with root system (if small) and part of the plant with branches, leaves, flowers showing maximum morphological characteristics useful for identification were collected for voucher preparation and plant identification. Plants were collected with all detail information of locality, plant habitat, road number, GPS coordinate, elevation level, field photograph, collector name, date, time etc.

Figure 1. Collection sites of medicinal plants for DNA barcode study of medicinal plants in Kingdom of Bahrain (Map Ref:

Plant vouchers were prepared with the proper sample ID after collection. Plant parts cleaned, and dried using spacers between layers of blotting papers and finally pasted on the Herbarium sheet with proper labelling. Field/Herbarium photograph taken and uploaded in the BOLD specimen submission portal and the records of each plant with pictures are traceable online in Plant Taxomony portal in BOLD system ( Plants identified and botanical names assigned based on reference books of Flora of Bahrain by ourselves. In some cases, we resolved the identification problem by consulting with taxonomists. Plants identified using standard identification method by comparing plant habitat, nodal characteristics of stem, leaf shape, leaf type, leaf arrangement, floral type, floral appearance, flower shape (sepal and petal), fruit characteristics etc.

2.3. Tissue Sample Preparation

Young leaves from the collected plant samples used for sample tissue preparation. Clean leaves properly dried either room temperature (thin and small) or heat dried at 37˚C (in case of succulents and thick leaves of desert plants). The leaves stored in sealable plastic packs and kept at room temperature [25].

2.4. Tissue Sub-Sample Preparation

As DNA was extracted using the plate based method, plant tissue sample of particular ID, around 2 - 3 pieces of plant leaves (0.5 cm) were subsampled in 96-well tube strips placed in plant box following the specific guideline of BOLD systems.

2.5. DNA Extraction

DNA extraction, PCR and sequencing work performed at Canadian Center for DNA Barcoding (CCDB), Canada using their standardized protocols. DNA extracted following the Glass fiber plate DNA extraction protocol, using a small amount of dry leaf samples [26] [27]. The leaf tissues were homogenized into fine powder using Tissue Lyser (Qiagen, USA) with rotated rack adopter at 28 Hz for 30 seconds by two times. DNA was extracted using 2X CTAB (250 µl) buffer and by incubating at 65˚C for 90 min. Cell lysates (50 µl) were transferred into 96-well Eppendrpf plate and Plant Binding Buffer (PBB, 100 µl) was added and incubated for 5 min at RT. 96-well Glass Fiber plate (PALL1) used and semi-automated glass fiber filtration method followed, while the corresponding DNA was bound to GF membrane [25]. GF Membrane rinsed by using Protein Wash Buffer (PWB) and the DNA eluted from GF plate to the collection microplate by adding pre-warmed double distilled water (60 µl), covered with cap strip and stored for PCR.

2.6. PCR and Sequencing

Three gene regions (rbcLa, matK, ITS2) were amplified using CCDB plant protocol [25] [26]. Amplification of the different plant markers required different primers and PCR recipes in PCR plates shown in Table 1 and Table 2. PCR plate placed into the thermo-cycling block and different PCR thermocycle programs were used for different primer set of three different barcode genes. Amplification of rbcLa: 94˚C for 4 min; 35 cycles of 94˚C for 30 sec, 55˚C for 30 sec; 72˚C for 1 min; final extension 72˚C for 10 min; hold at 4˚C. For ITS2: 94˚C for 5 min; 35 cycles of 94˚C for 30 sec, 56˚C for 30 sec, 72˚C for 45 sec; final extension 72˚C for 10 min; hold at 4˚C. Amplification of matK: 98˚C for 45 s; 35 cycles of 98˚C for 10 s, 54˚C for 30 s, 72˚C for 40 s; final extension 72˚C for 10 min; hold at 4˚C. PCR products visualized and analyzed on 2% Agarose E-gel R 96 system (Invitogen) using recommended program and software [27]. Strong amplification of rbcL and ITS2 were obtained using low concentration of primers, dNTPs and Taq polymerase with one primer set rbcLa-F [28] , rbcLa-R [29] and another primer set IITS-S2F [30] ITS4 [31]. In case of matK amplification, higher concentration of forward primer matK-xF [32] and reverse primer matK-MALPR1 [33] , dNTPs and Taq polymerase were used (Table 2). According to CCDB protocol, diluted PCR replicons used directly for sequencing [26]. PCR products were sequenced on an ABI 3730Xl DNA analyzer (Applied Biosystem, California, USA) following standard procedure. For bidirectional sequencing of rbcLa and ITS2, same PCR primer set used separately for bidirectional sequencing at 96˚C for 2 min; 30 cycles of 96˚C for 30 s, 55˚C for 15 s, 60˚C for 4 min; hold at 4˚C. For bidirectional sequencing of matK, three different primers used separately depending on PCR products used for sequencing at 96˚C for 2 min; 30 cycles of 96˚C for 30 s, 50˚C for 15 s, 60˚C for 4 min; hold at 4˚C.

2.7. Sequence Editing, Aligning, Assembly and Data Analysis

Chromatographs of all the three markers of those plants recovered, trimmed, edited and aligned by using Codon Code Aligner version 3.7.1-6.0.2 (CodonCode

Table 1. List of PCR primers and sequencing primers used in the DNA barcoding and identification of medicinal plants in Kingdom of Bahrain presented.

*Bidirectional Sequencing.

Table 2. Combinations and concentrations of reagents used for PCR reactions of rbcL, matK and ITS2 for analysis of medicinal plants of Kingdom of Bahrain presented.

*Platimum DNA Polymerase (Invitrogen, Carlsbad, California, USA) used for PCR reactions.

Co., Massachusetts, USA) by CCDB and received DNA sequences for further analysis and study. The nucleotide sequences of different plants aligned using Basic Local Alignment Search Tool (BLAST) algorithm provided by National Centre for Biotechnology Information (NCBI) and European Bioinformatics Institute (EMBL-EBI). The level of similarity between the samples studied by BLAST algorithm using blastclust (, which automatically and systematically clusters the nucleotide and protein sequences based on pairwise distance. It is a query method of genus and species of the samples from which sequences separated by the smallest genetic distances in the matrix [18]. The FASTA files of barcode sequences of rbcL, matk and ITS2 prepared for comparison with reference data sites. Different BLAST matching tools used widely to optimize the molecular data mining and for the identification of plants at genus as well as species level. This comparison brought out the genus identification and in some cases species identification. FASTA files of nucleotide sequences explored MUSCLE program [34]. The nucleotide sequences were aligned; analyzed and phylogenetic tree was constructed using various algorithm programs in Molecular Evolutionary Genetics Analysis (MEGA 7) software [35]. Sequence editing and alignment were generated by MUSCLE [34] to construct phylogenetic tree and evolutionary distance measurement by Kimura 2-parameter of studied plants [36]. The nucleotide sequences of coding region of chloroplast gene rbcLa, matK and nuclear ITS2 regions deposited in GenBank (Table 4).

3. Results and Discussion

3.1. PCR and Sequencing Success

The success of sequencing of barcode markers evaluated based on the number of plant species that successfully generated a sequence for a particular marker. The sequence recovery and analysis of three DNA barcodes of 29 medicinal plants collected from different parts of Kingdom of Bahrain showed (Figure 1). DNA barcodes genes of rbcLa, matK and ITS2 of 29 different medicinal plants representing 21 different families analyzed. The primers of rbcLa, matK, and ITS2 are used for PCR amplification, sequencing (Table 1) and PCR reagents (Table 2). For PCR amplification and sequencing of rbcLa and ITS2 same primers worked but in bidirectional sequencing of matK PCR products, 70% PCR products sequenced by choice I combination while 30% sequencing worked choice II (Table 1). The detail sequencing results of 29 medicinal plants of 21 different families using rbcLa, matK and ITS2 represented (Table 3). The success of sequence obtained of the 29 plants of three different barcodes genes rbcLa, matK and ITS2 were 97%, 79% and 75% respectively (Table 3). In bidirectional sequencing for rbcLa, forward primer gave high quality sequencing result in 92% plants while reverse primer gave 78%. In case of Limonium axillare in Plumbaginaceae and Mesembryanthemum nodiflorum of Aizoaceae, we got moderate quality sequencing product from forward primer and no product from reverse primer. High quality sequencing in matK and ITS2 obtained by 68% and 72% plants respectively using forward primer and 65% and 68% using reverse primer respectively. The high sequencing success rate of rbcLa (90%) than matK (70%) and ITS2 (41%) was observed in Amazonian trees while eight different DNA markers were tested [14]. In another DNA barcode study to build a community phylogeny of tropical trees, sequencing success was higher in rbcL region (90%) in comparing matK (68%) [37]. Sequencing success of rbcL (95%), matK (76%) and ITS2 (89%) from fresh specimen of vascular plants from Churchill was reported [38]. Similarly, the low success rate of matK in compare to rbcL reported in the speedy assessment of species abundance in taxonomically poorly known area or in cryptic population [39] , while, the sequence success of 88% and 90% in case of matK region is reported respectively by [20] [23]. The sequencing success of matK around 85% observed in standard and nested multiplex-tandem PCR [32]. In general, the lower success of matK sequence recovery also reflected due to difficulties in primer selection and binding of primers as explained [38] [39]. The low success of in sequence recovery in some genera may be relatively thick leaves of desert plants, slower desiccation and consequent DNA degradation [38]. It has been noted that rbcLa is much easier to sequence than matK and others, so the selection of rbcLa is an important option in barcoding study [40]. In several comparative studies, the variation in the success of sequencing results of different DNA may depend on the nature of plants, their habitat and ecological behavior [41]. The sequences of three different barcode genes submitted in GenBank (Table 4).

3.2. Identification and Comparison of Barcodes

The performance of the three-barcode markers for identification of plant genus and species level compared with Global multiple sequence alignment (MSA) and

Table 3. List of bidirectional sequence results of rbcL, matK and ITS2.

Primers used for sequencing were 1) rbcLa-F, 2) rbcLa-R, 3) ITS-S2F, 4) ITS4, 5) matK-xF, 6) matK-MALPR1, 7) matK-1RKIM-f and level of sequencing results mentioned as HQ: high quality sequencing and MQ: moderate quality sequencing.

presented (Table 5). The obtained sequence of the three barcode genes, rbcLa, matK and ITS2 analyzed following BLAST to confirm the taxonomic identification of the plants at the molecular level, using online database sites of International Nucleotide Sequence Database Collaboration (INSDC). The genetic distance (GD) between sequence pair and percent identity value (PI) after global multiple sequence alignment is helpful for comparative study, species identification and to score relatedness and distance. BLAST search data is helpful for

Table 4. List of submitted Genbank Accession Numbers of rbcLa, ITS2 and matK nucleotide sequences presented with plant Sample ID and plant name.

genus and species identification of plants at the molecular level, which is one of the main objectives of this study. This is helping in the process of plant taxonomical query in the regional and global accomplishment. Using NCBI database in BLAST analysis, 100%, 92.85% and 86.95% plant genus of the analyzed medicinal plants confirmed by obtained barcode sequences of ITS2, rbcLa and matK sequences respectively (Table 5). The use of rbcLa and ITS2 barcodes worked fine in compare to matK. Overall, 97% plants species were correctly

Table 5. The comparison of nucleotide sequences of three barcode genes of rbcLa, matK and ITS2 of medicinal plants in the Kingdom of Bahrain.

The percentage of plant identification at species and genus level calculated on the number of identified plants (genus/species level) based on total plants considered for the BLAST study.

identified either anyone of the barcodes (rbcLa, matK or ITS2) using BLAST survey. 28.57% plant species were confirmed by the analysis of all the three barcode sequences (rbcLa, matK and ITS2). 21.42% plant species were confirmed by the analysis of sequences of rbcLa and matK while 28.57% plant species were confirmed by the analysis of sequences of rbcLa and ITS2 combinations. 10.71% plant species were identified only by rbcLa (Limonium axillare, Herniaria hemistemon, Dipcadi erythraeum) and only by ITS2 sequences separately (Cynanchum variance, Cyanomorium coccineum, Cistanche coccineum). Only one barcode gene specifically confirmed the species identification using GenBank BLAST tool of those plants. BLAST analysis confirmed 100% medicinal plant genus and 89.28%, 86.32% and 60.86% plant species of medicinal plants by rbcLa, ITS2 and matK barcodes respectively. Similarly using BLAST analysis of sequence in the genetic distance analysis (GD), 99% success rate of genus identification and 73% and 75% species identification for rbcL and matK respectively observed in the identification of African rainforest trees was reported [18]. Similarly, the selection of rbcL and matK as core plant barcode marker reported by several workers and they have universal discriminatory power [14] [17] [42]. For identification of medicinal plant, the importance ITS2 together with rbcL, matK reported and justified that ITS2 is a valuable DNA barcode gene for the identification of closely related species [16] [30] [43]. Moreover, DNA polymorphism is typically low in coding plastid genes such as rbcL and matK but is frequent in noncoding ITS2 region and is helpful for species identification [18].

3.3. Phylogeny Study

The comparative analysis of molecular sequence data is essentially important for reconstructing evolutionary history of plants. The discriminatory influence of three barcode genes was considered in pairwise distance matrix to construct phylogenetic tree using in MEGA7 software [34]. The evolutionary history was inferred using pairwise distances in Maximum Composite Likelihood (MCL) [35]. The phylogenetic relatedness and evolutionary history drown by means of neighbor-Join (NJ) method [44] using nucleotide sequence alignment of rbcLa and ITS2 (Figure 2 and Figure 3). The evolutionary distance analysis conducted using Kimura 2-parameter [36] method of base substitution per site and mentioned

Figure 2. Molecular Phylogenetic affinity analysis of rbcL gene sequences of medicinal plants of Kingdom of Bahrain. The evolutionary history inferred using the Neighbor-Joining method [35]. The optimal tree with the sum of branch length = 0.88772833 is shown. The tree drawn to scale, with branch lengths in the same units as those of the evolutionary distances used to infer the phylogenetic tree. The evolutionary distances computed using the Kimura 2-parameter method [36] and are in the units of the number of base substitutions per site. The analysis included 28 nucleotide sequences of 28 plants and evolutionary analyses were conducted in MEGA7 [34].

Figure 3. Molecular Phylogenetic affinity analysis of ITS2 sequences of medicinal plants of Kingdom of Bahrain. The evolutionary history inferred using the Neighbor-Joining method [35]. The optimal tree with the sum of branch length = 1.30627545 is shown. The tree drawn to scale, with branch lengths in the same units as those of the evolutionary distances used to infer the phylogenetic tree. The evolutionary distances computed using the Kimura 2-parameter method [36] and are in the units of the number of base substitutions per site. The analysis included 22 nucleotide sequences of 22 plants and evolutionary analyses were conducted in MEGA7 [34].

by units. The pairwise distance matrix value indicates their closeness during evolution and ultimately helps to draw their phylogenetic tree and the history of evolution. The clades formed in the trees were mostly mixture of several plant species and the big and small branches showed their relatedness and distances clearly among the plant species. Cynanchum varians and Leptadenia pyrotechnica showed their closeness and common ancestry as they belong to the same family confirmed by taxonomic observation too. Similarly Herniaria hemistemon and Spargularia marina are closely related in their evolutionary history and belong to the same family Caryophyllaceae. In a double-locus (rbcLa and ITS2) phylogenetic trees, tree nodes and close branches supported the taxonomic clarity, relatedness and clade phylogeny. For each species, the higher interspecific distance obtained by ITS2 (33.17%) in compare to rbcLa (8.72%), so the value of closeness differed in phylogenetic tree of ITS2 (Figure 2) and rbcLa (Figure 3). Phylogenetic tree analysis of ITS2 and rbcL provided species resolution in a better way by using pairwise distance matrix value and indicated their closeness and distance with each other. Similarly, in the building of community parsimony, rbcL and ITS2 sequence alignment in constructing phylogenetic tress nodes showed support value in plant phylogeny [18] [29]. We noticed that the matK region of chloroplast genome is little problematic in sequence retrieving, phylogenetic data analysis and identification of plants in comparing to rbcLa and ITS2 barcodes, similar to other studies [17] [32] [42]. In the present study, rbcLa and ITS2 demonstrated excellent reliability for species authentication and less genetic diversity, due to the limited dispersal capacity in the plant communities of the arid and semiarid regions in comparison to tropics where it is frequent factor. So, the DNA barcode analysis of those plants is of a little bit challenging for species differentiation [18]. We noticed that the matK region of chloroplast genome is little problematic in sequence retrieving, phylogenetic data analysis and identification of plants in comparing to rbcLa and ITS2 barcodes, similar to other studies [17] [32] [42].

In conclusion, primarily, rbcLa and ITS2 are very useful barcode region and can be of wider application in the study of desert plant identification, ecology, and plant diversity study. Moreover, our sequences submitted to the GenBank will be of very helpful data for future study in various aspects. As, DNA barcoding has potentials to transfigure the systems of taxonomists work by giving considerable momentum during this era as a helpful tool for plant identification at molecular level.


The research was supported by the Research Grant # “TS-LS-BIOT.011_2015-2017” from College of Graduate studies, Agricultural Biotechnology Program, Department of Life Sciences, Arabian Gulf University. We like to Acknowledge CCDB for DNA analysis and sequencing work.

Conflicts of Interest

The authors declare no conflict of interest.

Cite this paper

Pathak, M.R., Mohamedm A.A.M. and Farooq, M. (2018) DNA Barcoding and Identification of Medicinal Plants in the Kingdom of Bahrain. American Journal of Plant Sciences, 9, 2757-2774.


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