Molecular identification of Lodoicea maldivica (coco de mer) seeds
© Mak and Mok; licensee BioMed Central Ltd. 2011
Received: 17 June 2011
Accepted: 30 September 2011
Published: 30 September 2011
The edible endosperm of Lodoicea maldivica with the common name of coco de mer is used in Chinese medicine for treating cough. Native to Seychelles, Lodoicea maldivica seeds have commanded high prices for centuries due to its scarcity. This study aims to develop a molecular identification method for the authentication of Lodoicea maldivica seeds.
DNA was extracted from the sample. Two polymerase chain reaction (PCR) systems were developed to amplify a region of the chloroplast DNA and the nuclear phosphoribulokinase (PRK) region specific to Lodoicea maldivica respectively. DNA sequence of a sample was determined and compared with that of the Lodoicea maldivica reference material.
The PRK gene of Lodoicea maldivica was successfully amplified and sequenced for identification.
A new molecular method for the identification of Lodoicea maldivica seeds in fresh, frozen or dried forms was developed.
Lodoicea maldivica (coco de mer), the sole member of the genus Lodoicea, is a fan-leaved palm native to Seychelles, bearing the largest and heaviest seed in the plant kingdom (weighing up to 30 kg). The seed is enclosed in a hard shell resembling a pair of coconuts joined in the middle. The seed is sometimes also referred to as the sea coconut, bum seed, double coconut, coco fesse or Seychelles nut. Lodoicea maldivica palms take between 25-50 years to reach maturity and bear fruit. The fruit may take one to three years to germinate . Only two natural populations of Lodoicea maldivica remain . Individual plants are also cultivated in various botanical gardens around the world. The harvest of seeds has virtually stopped all natural regeneration of the plant. The populations are also threatened by fire and encroachment by invasive plants. In March 2010, Lodoicea maldivica was added to the appendices of the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES) in its 15th meeting of the Conference of the Parties . Trade of Lodoicea maldivica is also governed by the Protection of Endangered Species of Animals and Plants Ordinance in Hong Kong (Cap. 586). According to the ordinance, unless exempted, the import, introduction from the sea, export, re-export or possession of Lodoicea maldivica requires a licence issued by the Hong Kong government. The edible endosperm (ie fruit) of the plant has long been used in Chinese medicine for treating cough and is used mainly in soup in Hong Kong, China . As fake products are often found in the markets, an identification method is needed.
This study aims to develop a new method for the identification of Lodoicea maldivica with DNA sequencing analysis. DNA was extracted from the edible endosperm sample. A polymerase chain reaction (PCR) system was designed to amplify a region of the chloroplast DNA to validate the quality of the extracted DNA [4, 5]. A number of genes or spacer regions may be considered to identify unknown samples, for example, the internal transcribed spacer 1 , internal transcribed spacer 2 , nuclear ribosomal RNA genes 18S unit , large subunit of ribulose 1,5-bisphosphate carboxylase/oxygenase (rbcL) , intergenic region between the β subunit of ATP synthase (atpB) and rbcL and the chloroplast trnL-trnF intergenic spacer region . In this study, a PCR system targeting the nuclear phosphoribulokinase (PRK) region was designed. This region has been employed in many palm phylogenetics and shown ample characters to resolve relations at species level [10–13]. After DNA sequence analysis, the identity of the unknown was evaluated by pair-wise matching of its sequence with that of the certified Lodoicea maldivica reference species.
Sample information and the results of their identities found
African seacoconut (dried)
99% [GenBank: (AF453357)]
For the samples in the form of pre-packaged product mixed with other materials, the suspected coconut portion was isolated from the background matrix before homogenisation. For fresh/frozen samples, the sample was homogenised by a blender, and about 1-5g of the sample was transferred into a flat bottom glass container. The sample was freeze-dried. The dried sample was ground into fine powder in liquid nitrogen. For dried samples, the sample was simply ground into fine powder in liquid nitrogen.
DNA extraction was performed with the CTAB method . A total of 1.0 mL of pre-warmed (65°C) CTAB extraction buffer (2% w/v hexadecyl trimethylammonium bromide (CTAB), 0.1 M Tris, 1.4 M NaCl, 20 mM EDTA) was added to 100 mg of the test sample in a 2.0 mL microcentrifuge tube. Alpha-amylase solution (10 μL-20 μL), 20 μL of proteinase K solution (20 mg/mL), 100 μL of 10% w/v polyvinylpolypyrrolidone (PVP) and 5 μL of RNase A (100 mg/mL) were added. The mixture was incubated at 65°C overnight with constant agitation. After centrifugation (Eppendorf, Germany) for ten minutes at 16,000× g at room temperature, the supernatant was transferred to a new 2.0 mL tube and an equal amount of chloroform was added. The sample was shaken vigorously for 30 seconds before centrifugation (Eppendorf, Germany) for ten minutes at 16,000× g at room temperature. The upper layer was transferred to a new 2.0 mL tube and extracted with an equal amount of chloroform. The sample was centrifuged 16,000× g (Eppendorf, Germany) for five minutes. The upper layer was transferred to a new 2.0 mL tube and two volumes of CTAB precipitation solution (0.5% w/v CTAB, 0.04 M NaCl) were added. The sample was incubated at room temperature for 60 minutes without agitation. The supernatant was discarded after the sample was centrifuged (Eppendorf, Germany) for ten minutes at 16,000× g. The precipitate was dissolved in 350 μL of 1.2 M NaCl solution and was centrifuged (Eppendorf, Germany) for ten minutes at 16,000× g. The upper layer was transferred to a new 1.5 mL tube. Two volumes of cold absolute ethanol were added to precipitate the DNA. The sample was kept at -20°C for at least 20 minutes. The supernatant was discarded after centrifugation (Eppendorf, Germany) for ten minutes at 16,000× g at 4°C. A total of 500 μL of 70% cold ethanol solution was added and the sample was centrifuged (Eppendorf, Germany) for ten minutes at 16,000× g at 4°C. The DNA pellet was dried in a 37°C oven for several minutes and was then re-dissolved in 100 μL of DNase-free water.
PCR for chloroplast DNA
Nucleotide sequences of specific primers used for the amplification of the chloroplast DNA and PRK gene
Oligonucleotide DNA sequence (5'-3')
Plant 1 (forward)
CGA AAT CGG TAG ACG CTA CG
Plant 2 (reverse)
GGG GAT AGA GGG ACT TGA AC
GTG ATA TGG AAG AAC GTG G
ATT CCA GGG TAT GAG CAG C
PCR for PRK gene
The PRK gene was amplified with 50 ng DNA template, 1.25 μL of 5 mM dNTPs, 2.0 μL of 25 mM MgCl2, 2.5 μL of 10× PCR buffer without MgCl2 (Applied Biosystems, USA), 1.5 μL of 10 μM specific primers (Table 2), 1.25 μL of 40 ng/μL bovine serum albumin (BSA), 0.5 μL of dimethyl sulfoxide (DMSO) and 1 U of AmpliTaq Gold polymerase (Applied Biosystems, USA). Water was added to make up the final volume to 25 μL. The DNA template was denatured at 95°C for four minutes, and then 35 cycles of one minute at 94°C, 30 seconds at 54°C, one minute at 72°C and final extension at 72°C for seven minutes. The amplification products were electrophoresed on a 1% agarose gel, stained with ethidium bromide and observed under UV illumination.
The PCR products of PRK gene were purified with DNA Clean & Concentrator™ -25 (Zymo Research, USA) according to the manufacturer's instructions. The BigDye® Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems, USA) was used for the cycle sequencing reaction. The PCR product was first denatured at 96°C for one minute and then 25 cycles of thermal cycling was performed as follows: 96°C for ten seconds, 50°C for five seconds, 60°C for four minutes. The BigDye® XTerminator™ Purification Kit (Applied Biosystems, USA) was used to purify the extension products according to the manufacturer's instructions and the products were then run on the ABI PRISM® 3130XL Genetic Analyzer (Applied Biosystems, USA).
We aligned the sequence of the unknown sample in pair with that of the reference species using the bl2seq tool of the National Center for Biotechnology Information (NCBI) website . Moreover, we performed multiple sequence alignment using the CLUSTAL2 tool of the European Bioinformatics Institute website .
Results and Discussion
A study  reported that DNA from the solid endosperm of coconut was not a good starting material for molecular biology work because the matrix may hinder enzyme activity and because of the high lipid and polysaccharide content. The study suggested that DNA from young leaves of the plant should be used as the source of genomic DNA. Nevertheless, only the edible endosperm of Lodoicea maldivica is used in Chinese medicine and the commercial products thereof are made up of various forms of its edible endosperm. In order to develop a method for testing the authenticity of the claimed Lodoicea maldivica products, we think that PCR-ready DNA must be extracted from the endosperm of Lodoicea maldivica.
The chemical PVP is an important reagent in DNA extraction. Without the addition of PVP, the sample solution for the extracted DNA contained high levels of polysaccharide, as shown in the UV spectra. The contamination was greatly reduced by the addition of PVP during the initial incubation at 65°C in the extraction step. While the amount of DNA extracted from all samples in this study was very low (< 10 ng/μL), the quality of the extracted genomic DNA was sufficient for the PCR and sequencing.
Plant 1 and Plant 2 primers are targeted for the amplification of a region of plant chloroplast DNA and were used to verify the quality of the template DNA . A single PCR product of about 550 bp was successfully amplified from all samples. The positive PCR results indicated that DNA of sufficient quantity and quality were successfully extracted and that the PCR was not inhibited by other components of the analytical sample.
PCR PRK gene
The nuclear region of the PRK gene was amplified with the second PCR system. This region has been used successfully to resolve palm phylogenetic relations at the species level [10–13]. Positive results (ie a fluorescent DNA band of about 750 bp) from this PCR system would indicate that the sample contained the PRK gene whereas negative results would indicate that the sample was not from Lodoicea maldivica.
Single-band PCR products of about 750 bp were successfully amplified from Lodoicea maldivica reference material and two commercial products namely Sample A and Sample H. Other samples yielded either negative results or multiple PCR products in the amplification of PRK gene. Lodoicea maldivica yielded only one single PCR product in the analysis of PRK gene. The sample should be considered as not of Lodoicea maldivica in origin when no or more than one band was observed after agarose gel electrophoresis . The identities of these unknown samples were found by using one of the markers [6–9] as mentioned in the background section.
A new molecular method for the identification of Lodoicea maldivica seeds in fresh, frozen or dried forms was developed.
This article does not necessarily reflect the views of the Government of the HKSAR. The mentions of trade names or commercial products do not constitute any endorsement or recommendations.
Convention on International Trade in Endangered Species of Wild Fauna and Flora
hexadecyl trimethylammonium bromide
National Center for Biotechnology Information
polymerase chain reaction
The authors would like to thank Dr CM Lau, Government Chemist of the Government Laboratory of the HKSAR, China, for his support and encouragement during the study. We would also like to thank Dr Della WM Sin and Ms Silvia YK Tam for their discussion and comments.
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