Patent Application
20180216168
The present invention relates to a diagnostic kit, able to identify particular strains of the nitrogen-fixing bacteria Gluconacetobacter diazotrophicus (Gd) that have good utility in agriculture, in terms of their ability to colonise plant cells intracellularly, giving rise to particularly effective nitrogen fixation, as well as to reagents for use in the kits. Novel strains that are identified by the kits form the subject of a co-pending application.
Gluconacetobacter diazotrophicus (Gd) has been well studied for its nitrogen fixing and plant growth promoting activities as reviewed in Eskin et al. International Journal of Agronomy (2014):1-13. Certain strains of Gd however have been shown to be particularly advantageous in the treatment of plants since they are able to establish themselves intracellularly within plant cells along with exhibiting species and tissue independence (Cocking et al., In vitro Cellular & Developmental Biology Plant (2006) 42 (1). These properties, combined with their ability to travel throughout a range of plant tissues, make such strains better able to deliver the benefits to the target crop plants.
However, a wide range of strains of Gd exist and it has not yet been possible to provide a means for easily identifying strains which have these beneficial properties.
Furthermore, an important aspect of bio-fertiliser has been to provide an alternative to the chemical fertilisers in a nature friendly way to agricultural crop plants. However, it would be helpful to validate the effectiveness of any on-going treatment in field conditions, so that a farmer is able to determine what levels of nitrogen fertiliser, if any, are required to be supplied to enhance growth conditions.
The applicants have found that specific advantageous strains of Gd contain a number of unique nucleic acid sequences that are not found in other Gd species, nor in any other species, including plant species. This gives rise to the provision of a reliable diagnostic test, useful in both monitoring of treatments in the fields and in research, for identifying related beneficial strains.
According to the present invention there is provided a diagnostic kit comprising means to determine the presence in a sample of at least one nucleic acid sequence selected from SEQ ID NOS 1-10 shown in attached Table 1 hereinafter.
SEQ ID NOs 1-10 represent unique and novel sequences, which appear in a preferred sub-species or strain of Gd. Strains having these unique characteristics have been found to be particularly effective in intracellular colonization of plant cells resulting in beneficial nitrogen fixing. In particular, it has been found that use of a stain of the invention leads to yield enhancements in crops such as cereal crops like maize and wheat. Alternatively, similar yields can be achieved even with reduction in traditional nitrogen fertiliser applications.
Thus the sequences provide a means for identifying these beneficial strains. In addition, they have been found to be amenable to detection using primers which do not cross-react with plant species.
Furthermore, since the strains can colonise intracellularly in the host plant cells, they are able to effectively travel throughout the plant. The kit of the invention can be used to provide an evaluation of colonisation by Gd post-germination at a young stage and check its efficiency. This will then allow the farmers to make an “informed decision” about the existence and extent of the colonisation and if required how much chemical based nitrogen fertiliser will be required to be applied. This extra level of security will provide ‘assurance’ to farmers that their crops are being well-tended, even when using nature and crop friendly fertiliser in the form of Gd.
In a particular embodiment, the kit of the invention comprises means for determining the presence of more than one of the nucleic acid sequences of SEQ ID NOs 1-10, for example up to 10, such as up to 5, or up to 3 of said nucleic acid sequences of SEQ ID NOs 1-10. In this way, a reliable diagnostic kit would be provided which will ensure that the strain detected is the one which is similar or substantially similar to the beneficial strain. Similar strains would be detected even if one or more of the sequences differs for example as result of mutation.
Preferred strains appear to contain a plasmid, and so plasmid detection, for example by isolation using a commercially-available plasmid isolation kit, may provide further confirmation of the identification of a beneficial strain. In particular, any plasmid identified should be less than 27455 bp in size, for example about 17566 bp. The presence of a plasmid, in particular of this size, differs from a previously known strain of Gd, UAP5541, which has been reported as lacking in plasmids (Luis E. Fuentes-Ramièrez et al., FEMS Microbiology Ecology 29 (1999) 117-128). Furthermore, the size of the plasmid is smaller than that reported previously in respect of PAL5 strains containing a single plasmid (Giongo et al. Standards in Genomic Sciences, May 2010, Volume 2, Issue 3, pp 309-317 doi: 10.4056/sigs.972221).
The plasmid of beneficial strains may also be characterized in that it is restricted into two fragments by the restriction enzyme EcoRI, wherein the fragments are about 12 Kb and about 5.6 kb in size respectively. Thus, in certain embodiments, the kit of the invention may further comprise means for determining the presence and nature of the plasmid, including the provision of a restriction enzyme such as EcoR1, to allow for the detection of fragments of the above-mentioned sizes.
Furthermore, the plasmid lacks a number of key sequences which have been previously identified as being present in the plasmid of PAL5. These sequences are shown as SEQ ID Nos 65, 66, 67 and 68 in the attached sequence listing. Thus the absence of these particular sequences may provide a further characterizing feature of the strains. In some embodiments therefore, the kit may comprise means for detecting these SEQ ID Nos 65, 66, 67 and 68 to provide a negative control in the sense that the absence of positive results for these sequences may be used to confirm the presence or identity of preferred strains, or the presence of the these sequences may be used to reject less preferred strains in strain selection.
In a particular embodiment, the diagnostic kit further comprises means for determining the presence of at least one nucleic acid sequence which is characteristic of Gd species, for example 2, or 3 nucleic acid sequences which are characteristic of Gd species. In this way, the kit would provide confirmation that some Gd is present in the sample, thus confirming the accuracy of the test. If the sample is known to contain Gd, a positive result in this determination would act as a ‘control’ confirming that the test has been carried out effectively. Suitable specific strains will be sequences found in Gd species generally but not in other species, and in particular not in other microbial species or in at least some plants, in particular plants which may be targeted for Gd treatments.
Particular examples of such sequences are shown as SEQ ID NOS 11-13 in Table 2 hereinafter. In particular, these nucleic acid sequence which is used to detect Gd species have been found to be amendable to detection of Gd species present in a range of crops, without cross-reacting with plant species.
In a further embodiment, the kit comprises means for detecting the presence of a plant specific nucleic acid sequence, such as a chloroplast specific nucleic acid which amplifies universally from plant DNA. The inclusion of such means will act as a control when the kit is used in the context of detection of Gd within a plant species, as this means will produce a detectable signal, even in the absence of any Gd. If this signal fails, this would indicate failure in the test rather than necessarily that there is no Gd present. A particular chloroplast primer set which is available commercially from Thermo Scientific. Product as Phire Plant Direct PCR Master Mix, is based on the disclosure by Demesure B et al (1995) Molecular Ecology 4:129-131.
The means for detecting the presence of the nucleic acid sequences may take various forms as would be understood in the art.
Where the nucleic acids are genes which are expressed, the kit may comprise means for detecting the expressed proteins. Such means may include specific protein tests such as immunochemical analysis which utilise antibodies specific to the proteins to immobilise and/or detect the proteins, such as ELISA or RIA techniques, or immunoelectrophoretic methods such as Western blotting.
However, in a particular preferred embodiment, the kit of the invention comprises means for detecting specific nucleic acids themselves.
In particular, nucleic acids may be detected using any of the available techniques including nucleic acid binding assays and immunoassays using antibodies raised to haptenised forms of the nucleic acids. However, in a particular embodiment, the detection involves nucleic acid amplification reactions, and thus in particular, the kits will comprise one or more amplification primers which target the or each nucleic acid sequence being detected.
As would be understood by a skilled person, when detection of a sequence is carried out using an amplification reaction, it would not be necessary to amplify the entire sequence, but rather just a characteristic fragment of the entire sequence, for example a fragment of at least 10, and suitably at least 50 base pairs. Thus the size of the sequence that may be amplified would could be in the range of from 10-3070 base pairs, and suitably from 20-2000 base pairs, for example from 50-500 base pairs, such as from 100-300 base pairs. The size of the fragment will depend upon the nature of the detection reaction being used, but it should be sufficient to ensure that the product is characteristic of SEQ ID Nos 1-10 or variants as defined above, and so is not present in other sequences, in particular plant sequences. Where more than one sequence is amplified, they may be selected to be of differing sizes, so that they may be easily differentiated during detection, using techniques such as separation on the basis of size, or melting point analysis.
If required, the kit may further comprise one or more additional reagents necessary to carry out a nucleic acid amplification reaction. Thus it may include enzymes such as polymerases, salts such as magnesium or manganese salts, buffers and nucleotides as would be understood in the art.
The kits may, if required, include means for detecting the products of the amplification. Such means may include dyes or probes, in particular labelled probes that bind the target sequence intermediate the primers. Alternatively, the primers themselves may be labelled to facilitate detection.
Suitable nucleic amplification reactions include reactions that utilise thermal cycling such as the polymerase chain reaction (PCR) and ligase chain reaction (LCR) as well as isothermal amplification reactions such as nucleic acid sequence based amplification (NASBA), strand displacement amplification (SDA), transcription mediated amplification (TMA), loop-mediated isothermal amplification (LAMP) and rolling circle amplification, 3SR, ramification amplification (as described by Zhang et al., Molecular Diagnosis (2001) 6 No 2, p 141-150), recombinase polymerase amplification (available from TwistDx) and others. In a particular embodiment, the nucleic acid amplification is a PCR, and may be a quantitative PCR (QPCR) to provide information regarding the extent of colonisation.
In an alternative embodiment, the amplification is LAMP reaction. LAMP assays utilise at least four and suitably six primers which are designed to target six different regions of the target sequence. There will always be two outer primers (F3 and B3) and two inner primers (FIP and BIP). Optionally, in addition there are two loop primers (FLoop and BLoop). The use of the Loop primers usually reduces the amplification time and increases the specificity of the assay. FIP and BIP primers consist of F2, complementary to the F2c region of the template sequence, and F1c, identical to the F1 region of the template. Four main features need to be considered in order to guarantee a successful LAMP primer design: the melting temperature of the primers (Tm), given 55-65° C. for F3, FIP, BIP and B3 primers and ≥65° C. for FLoop and BLoop; a GC content of 50-60% in the primer sequences; the absence of secondary structures formation and stability at the ends of each primers; and finally the distance between primer regions. Examples of suitable LAMP primer sets are disclosed hereinafter.
The presence of the products of amplification reactions may be determined using any available technology. Thus they may include techniques where products are separated on a gel on the basis of size and/or charge and detected such as agarose gel electrophoresis. Alternatively, they may be detected in situ, using for example using intercalating dyes or labelled probes or primers. The detection of amplification products using a wide variety of signalling and detection systems is known. Many of these systems can be operated in ‘real-time’, allowing the progress of amplification to be monitored as it progresses, allowing for quantification of the product. Many such systems utilise labels and in particular fluorescent labels that are associated with elements such as primers and probes used in the amplification system and which rely on fluorescent energy transfer (FET) as a basis for signalling. A particular form of such fluorescent energy transfer is fluorescent resonance energy transfer or Förster resonance energy transfer (FRET) for signal generation.
A major example of such a process used commercially is the TaqMan® process, in which a dual-labelled probe, carrying both a first label comprising a fluorescent energy donor molecule or reporter and a second label comprising a fluorescent energy acceptor molecule or quencher, is included in a PCR system. When bound to the probe, these molecules interact so that the fluorescent signal from the donor molecule is quenched by the acceptor. During an amplification reaction however, the probe binds to the target sequence and is digested as the polymerase extends primers used in the PCR. Digestion of the probe leads to separation of the donor and acceptor molecules, so that they no longer interact. In this way, the quenching effect of the acceptor is eliminated, thus modifying emissions from the molecule. This change in emission can be monitored and related to the progress of the amplification reaction.
Where more than one nucleic acid sequence is detected, the kit may comprise components sufficient to carry out multiple separate amplification reactions, such as individual sets of primers. Preferably however the kit is set up to carry out a multiplex reaction, where multiple targets may be detected in a single reaction. In this case, where the detection is done using gel electrophoresis, the primers are suitably selected so that each amplified product has a significantly different size or charge so that they may be readily separated and identified on an agarose gel or by melting point analysis using a signalling reagent such as a DNA intercalating dye.
Alternatively, where the detection system includes labels, any labels provided for example on primers or probes, will provide a different and distinguishable signal from other primer sets, for example on the basis of the wavelength of the emitted signal and/or the fact that the product has a different melting point or annealing temperature, which may be distinguished by carrying out a melting point analysis of products.
Suitable amplification primers, in particular for PCR amplification, together with the approximate size of the products they generate are selected from those set out in Table 3 below:
Primer sets represented by SEQ ID NOS 14-33 have been found to act as useful strain-specific primers for beneficial strains of Gd, while primer sets represented by SEQ ID NOS 34-39 act as useful Gd species-specific primers.
In a further aspect, the invention provides a method for determining the presence in a sample of a strain of Gluconacetobacter diazotrophicus (Gd) able to intracellularly colonise plant cells, said method comprising detecting in said sample at least one nucleic acid sequence selected from SEQ ID NOS 1-10.
Suitably up to 10, for example up to 5 such as about 3 of said nucleic acid sequences of SEQ ID NOs 1-10 are detected.
In a particular embodiment, the method further comprises detecting at least one nucleic acid which is characteristic of Gd species, as described above, such as a nucleic acid sequence of SEQ ID NOS 11-13. Again, more than one such species specific nucleic acid sequence may be detected if required.
In yet a further embodiment, the method further comprises detecting a plant specific nucleic acid sequence, which may be characteristic of the particular Gd colonised plant being examined or may be universally present in plants, such as a chloroplast specific nucleic acid sequence, as a control for the reaction.
Various methods of detection may be used in the method, as described above, but in particular, the method comprises a nucleic acid amplification reaction, such as the polymerase chain reaction (PCR).
Suitable primers are as described above.
The sample which may be used in the method of the invention may be any sample that contains or is suspected of containing a strain of Gd. This may include cultures or laboratory samples, which may contain the desired strain of Gd. Alternatively, they may comprise plant samples, including leaf, stem, or root samples, from which nucleic acid has been released, for example by causing cell lysis, for example using mechanical, chemical or sonic means. In particular, the sample is from a plant to which a strain of Gluconacetobacter diazotrophicus (Gd) has previously been applied. In this way, the successful colonisation of the plant by Gd can be confirmed.
Typically, such tests will be carried out in a laboratory, although mobile testing, for example, in field conditions, may be carried out if suitable equipment, such as mobile PCR machines, are available, or if detection of targets in particular protein targets, using techniques such as ELISAs, which may be carried out on lateral flow devices are employed.
Novel strains of Gluconacetobacter diazotrophicus (Gd) able to intracellularly colonise plant cells and identified using a method described above are described in the applicants copending application of even date. A particular example of such a strain IMI504958, deposited at CABI (UK) on 22 May 2015.
The invention will now be particularly described by way of example with reference to the accompanying figures which are described as follows:
However, it will be apparent to one skilled in the art that the specific details are not required in order to practice the invention. The following descriptions of specific embodiments of the present invention are presented for purposes of illustration and description. They are not intended to be exhaustive of or to limit the invention to the precise forms disclosed. Many modifications and variations are possible in view of the above teachings. The embodiments are shown and described in order to best explain the principles of the invention and its practical applications, to thereby enable others skilled in the art to best utilize the invention and various embodiments with various modifications as are suited to the particular use contemplated.
IMI504958, a Gd strain derived from passaging UAP5541, which was found to have particularly beneficial plant colonisation properties was isolated and the full genome sequenced. A comparison was made against the publically available genome of the type strain (PAL5; sequenced by JGI, USA [Genbank sequence accession CP001189]) using standard methods.
Surprisingly, a large number of differences were noted in the genome, and in particular, a number of genes were identified which are present in the genome of IMI504958 but not PAL5.
Many of these genes were annotated with an associated function. The unique genes with annotations were further checked for uniqueness across all the genomes sequenced to date using the NCBI's web-based BLAST tool.
Analysis of the BLAST result narrowed the list to 20 unique genes not present in any genome. These unique genes appeared to be “strain-specific” for IMI504958.
Also, five sets were found to be unique to the Gd species and will hereafter be referred to as “species-specific” (i.e. present in IMI 504853, Pa15 and other Gd strains but in no other species).
The applicants used this data to design a diagnostic kit for IMI504958.
A set of 25 primer sets were designed based upon the sequences identified in the analysis of the genome. The specificity of these 25 primer sets (20 designed to be strain-specific and 5 designed to be species-specific) were first tested by carrying out a conventional PCR reaction using genomic DNA of IMI504958 and PAL5. The results with IMI504958 are illustrated in
All 5 species-specific primers reacted as expected.
Further, testing of strain- and species-specific primers was done against two other strains of Gd, one originally isolated in India (IMI 502398) and the other from Mauritius (IMI 502399), as well as a revived 2001 culture of UAP5541 strain (stored in glycerol at −80° C.), using the method described above. The data was in agreement with the 16 strain specific primers and 4 species specific primer sets as one of the species-specific primer sets produced a higher molecular weight band. This was a surprise result.
The sensitivity of detection of all 25 primer sets (20 strain-specific and 5 species-specific) was checked using serial dilutions of bacterial broth cultures. It was found that 24 of these sets produced very high levels of detection (requiring 1-10 bacterial cells).
Further, these 25 primers were then checked for cross-reactivity with several target plant species and varieties using DNA extracted in-house. The primers were tested in a PCR reaction using DNA extracted from plants of the following species: maize, wheat (var. Willow), quinoa, rice (var. Valencia), barley (var. Chapeaux), potato, Arabidopsis (var. Columbia), oilseed rape (vars. Ability and Extrovert) and a range of grasses (vars. Aberglyn, Dickens, J Premier Wicket, and Twystar). The method for isolating nucleic acids from plant tissues involved the mechanical maceration of leaf material followed by a modified CTAB extraction (Doyle and Doyle, 1987 Phytochem. Bull., 19: 11-15). Briefly, cellular membranes were disrupted using SDS and CTAB to release their contents, and cellular proteins were degraded or denatured using proteinase K and β-mercaptoethanol. The extraction buffer also contained PVPP to remove plant polyphenols, EDTA to chelate metal ions, sodium chloride to solubilise nucleic acid structures, as well as TRIS HCl to stabilise the buffer pH. RNA molecules were degraded using RNase A treatment. Following the removal of insoluble cellular debris using chloroform:isoamyl mix (24:1), deoxynucleic acids were precipitated in ethanol using sodium acetate, washed using diluted ethanol, and resuspended in molecular grade water.
Illustrative results are shown in
At the same time, the sensitivity of primers were tested by co-inoculating PCR reactions containing 100 ng of the above mentioned plant genomes with six-fold serially diluted genomic DNA from Gd, starting from 1 ng. It was found that the sensitivity of the PCR system was generally unaffected by the presence of plant genome and routine detection was established from a minimum of 1 picogram of Gd DNA.
Illustrative results are shown in
Results suggested that 17 of the 20 strain-specific primer sets and three of the five species-specific sets either do not cross react with any plant genomes tested, or cross-react with a small number but produce a DNA product of a different size and distinguishable size.
Of the strain-specific primer sets, only 10 produced results which were of (1) high specificity, (2) high sensitivity, and (3) produced no cross-reactions with plant DNA and these are represented in Table 3 above as primer sets A-J. Similarly only three of the selected species-specific primer sets were found to be specific and sensitive enough for use and these are shown as primer sets K-M in Table 3 respectively. In addition, the size of the products obtained using these primers is shown in Table 3 and illustrated in
A series of LAMP primers were designed to amplify regions of SEQ ID NOS 6, 7 and 9 and are shown in Table 4 below as follows:
SEQ ID NOS 40-45 were designed to amplify SEQ ID NO 6 above, SEQ ID NOS 46-51 were designed to amplify SEQ ID NO 7 above, and SEQ ID NOS 52-57 were designed to amplify SEQ ID NO 9 above.
These primers were obtained and tested in a LAMP assay on samples comprising pure Gd DNA that had been isolated using a modified CTAB methodology from bacteria grown in liquid culture.
In addition, DNAs from a range of plant pathogenic bacteria and fungi was tested for amplification in LAMP by the primer sets. These included Bacillus subtilis, Lactobacillus, Fructobacillus, Pseudomonas spp., Agrobacterium spp., a range of phytoplasmas and various fungi including species from the Fusarium, Penicillium and Aspergillus genera.
Real-time LAMP was carried out on a Genie II instrument (OptiGene), and 1 μl of sample was added to a 24 μl reaction mix containing 15 μl Isothermal Master Mix ISO-001 (OptiGene), 200 nM of each external primer (F3 and B3), 2 μM of each internal primer (FIP and BIP) and 1 μM of loops primer (FLoop and BLoop). RT-LAMP reaction consisted of 30 minutes of isothermal amplification at 63° C. To evaluate the annealing temperature of the products, reactions were then subjected to a slow annealing step from 95 to 68° C. (0.05° C./s) with fluorescence monitoring.
Negative reaction controls, consisting of water, were also used.
Of the three sets of primers tested in LAMP, the third primer set specific for SEQ ID NO 9 gave amplification in nine and a half minutes with an anneal at 89.2° C. (see
All sets of primers that gave the positive Gd amplification were specific for the bacterium and did not amplify from DNA of any of the other bacterial and fungal DNAs they were tested on. They are therefore all suitable as primer sets to be used for detection of the Gd bacterium.
To validate the primers on rapidly extracted DNA from contaminated seed, a series of experiments were set up in which seed of two plant species, tomato and wheat, were spiked on the surface with Gd DNA. The samples were then put through the 2-minute DNA extraction technique in which the samples are placed in plastic tubes containing steel beads and TE buffer and shaken vigorously for 2 minutes. Two microliters of the solution was then placed in the LAMP reaction as described in Example 4 using the primer set comprising SEQ ID NOs 52 to 57 to test for amplification of the Gd DNA from these samples.
The results showed that the Gd DNA is detectable when put through these assays, against a background of plant DNA.
In order confirm that any samples that tested negative for Gd supported LAMP amplification (i.e. they do not contain inhibitors of LAMP reactions), the cytochrome-oxidase gene (COX) primers (Tomlinson et al., 2012 Journal of Virological Methods, 191: 148-154.), which amplify DNA from the host plant, were used as controls for false negatives on all samples.
A range of QPCR reactions were carried out on samples comprising known quantities of DNA from Gd (IMI504958) and also from a range of crop species including maize, barley and wheat genomic DNA.
QPCR reaction mixtures were prepared to a volume of 20 μL volume per reaction. In the case of Gd DNA alone, these consisted of 10 μL iTaq™ Universal SYBR Green® Supermix (2×) (Bio-Rad), 1 μL each of forward and reverse primers (final concentration of 10 μmol), 7 μL SDW (sterile distilled water) and 1 μL DNA template at the required concentration.
Primers used in this case were as set out in Table 5.
The primer set represented by SEQ ID NOs 58 and 59 (designated P5) was aimed at amplifying a 149 base pair region of SEQ ID NO 3, the primer set represented by SEQ ID NOS 60 and 61 (designated P8) was designed to amplify a 104 base pair region of SEQ ID NO 6 above, and the primer pair represented by SEQ ID NO 62 and 63 (designated P17) was designed to amplify a 130 base pair region of SEQ ID NO 10 above.
Thermocycling was carried out using a CFX96 Touch™ Real-Time PCR Detection System from Bio-rad. Initial denaturation was performed at 95° C. for 3 minutes; amplification was performed using 40 cycles of denaturation at 95° C. for 5 seconds followed by 60° C. for 30 seconds (plate read post each amplification).
All of the primer sets amplified Gd DNA with good efficiency as set out in Table 6, which shows the average Cq values of three replicates of the amplification, and quantitatively as illustrated by
The quantitative amplification was carried out in the presence of genomic plant DNA in order to determine whether there was any cross reactivity. It was found that whilst there was cross reactivity with some plants species, the primer pairs P5 showed no cross-reactivity to wheat and barley genomes, P8 showed no cross-reactivity to wheat barley and maize and P17 showed no cross-reactivity to wheat and maize genomes making these potentially suitable primer sets for detecting Gd in crop species.
To ensure that primer efficiency and robustness would be maintained in the presence of plant genomic DNA, the above QPCR examples above were repeated but in this case, the composition was varied in that 6 μL SDW (sterile distilled water) was used together with 1 μL relevant Gd dilution DNA template and 1 μL plant genomic DNA template. For instance, Gd DNA (92 ng/μl) was serially diluted from 10−1 to 10−7 with either wheat DNA (70.6 ng/μl) or maize DNA (111 ng/μl) and amplification reactions run as described above.
Representative results are shown in
It appears that the primers will maintain efficiency in the presence of plant genomes and thus may form the basis of a detection kit.
Results were confirmed by carrying out melt analysis post amplification the denaturation curve (Melt curve) analysis was performed from 60° C. to 95° C. with 0.5° C. increment 5 seconds/step followed by plate read after each increment.
Representative examples of the results are shown in
Plasmid DNA extraction from Gd (IMI504958) was performed using Qiagen mini prep kit (Cat. No. 69104). The low copy number plasmid extraction protocol was followed using 5 ml and 10 ml 48 hour bacterial culture. The extracted plasmid was run on 1% agarose gel flanked by a 1 kb ladder (
Alongside the plasmid DNA, genomic DNA of Gd (IMI504958) was also included on lane-1. The results, shown in
The plasmid DNA was sequenced and a primer was designed using Primer3 to cover the start and end sites of linear sequence data (P_End_Fw—CCAAATCTCTGGAACGGGTA (SEQ ID NO 64). Sangar sequencing was performed using this primer (SEQ ID NO 64) and the sequenced data was aligned to confirm the plasmid sequence was complete.
Since plasmid DNA in its natural form is circular and can form secondary and tertiary structures, this may impact on the accuracy of size measurements using agarose gels. To confirm the results and also validate the sequencing of the plasmid DNA, a restriction map of plasmid was studied using NEBcutter. The restriction digestion will linearize the plasmid providing only a single conformational structure. Also, the restriction enzyme selection is done after studying the sequence, thus allowing the plasmid sequence to be validated as well. In case of IMI504958 plasmid DNA, the NEB-cutter showed the restriction enzyme EcoRI to digest the plasmid DNA at 3864-9461 bp and 9462-3863 bp producing a DNA fragment of 5598 bp and 11968 bp. Both the size can be studied using a 1 Kb ladder available in the lab, removing the limitation of the reference ladder's maximum size detection as well.
Therefore, restriction digestion was performed on IMI504958 plasmid using double cutter EcoRI as per supplier's protocol. Post restriction digestion the products were run on 1% agarose gel until the bands were resolved and imaged. IMI504958 plasmid DNA when restricted with EcoRI produced two fragments (1. ˜12 Kb and 2. ˜5.6 Kb) of DNA of predicted size (
This validated the sequencing data in terms of both size and sequence. It may further provide an identification test or a confirmatory test in relation to the kit of the invention.
A field trial was designed to test Gd (IMI504853) as a bio-fertilizer using wheat (cultivar Mulika). Two plots of Gd treated and control (untreated) respectively where planted. Post germination the young wheat seedlings at 10-12 day of growth were sampled and tested for Gd presence using the primer G (seq ID 26 & 27) representing the DNA seq ID 7. The Gd presence was detected when PCR was resolved on a 1% agarose gel with respective negative and positive controls (
The measurement of chlorophyll content i.e. “greenness” using a SPAD meter has been shown to correlate with over all plant health and crop yield. The crop at growth stage 35 and 61 were checked for its chlorophyll content using SPAD was found to be statistically significantly (P=0.001) in Gd treated plots when compared to control plots (
| Number | Date | Country | Kind |
|---|---|---|---|
| 1513277.2 | Jul 2015 | GB | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/GB2016/052288 | 7/27/2016 | WO | 00 |
