02751nas a2200277 4500008004100000022001400041245012500055210006900180260006400249300001200313490000800325520173500333653000902068653003702077653003202114653000902146653001302155653002102168653003002189653004702219100002002266700002002286700002002306700001702326856013002343 2009 eng d a0027-551400aIdentification of Indian pathogenic races of fusarium oxysporum f. sp ciceris with gene specific, ITS and random markers0 aIdentification of Indian pathogenic races of fusarium oxysporum  a810 E 10TH ST, LAWRENCE, KS 66044 USAbALLEN PRESS INCcAUG a484-4950 v1013 a

In this study we demonstrate the synergistic use of gene-specific markers, ITS-RFLP, ISSR and AFLP for distinguishing Indian F. oxysporum f. sp. ciceris races. We also report for the first time that F. oxysporum f. sp. ciceris race 3, a wilt pathogen of chickpea in India, is actually E proliferatum based on phylogenetic analysis with EF-1 alpha sequence data. E oxysporum f. sp. ciceris races 1, 2 and 4 were easily distinguished from ``race 3'' (F. proliferatum) by PCR amplification with oligonucleotides designed from conserved regions of Hop78 transposon (Hop 78), cutinase (Cut), desaturase (Dst). F oxysporum f. sp. ciceris race 4 was distinguished with the xylanase 3 (xyl3) gene by absence of amplification product only in this race. The Xyl3 amplified-DNA fragment isolated and sequenced from E oxysporum f. sp. ciceris race I was similar to the F-xylanase (Xyl3) gene of E oxysporum f. sp. lycopersici. A TELD motif, which is characteristic of the F-xylanases family, was detected within the deduced amino acid sequence of F. oxysporum f. sp. ciceris. Similarly the F oxysporum f. sp. ciceris Hop78 DNA fragment, which identified ``race 3'' (E proliferatum), was homologous to the Hop78 transposon of E oxysporum f. sp. melonis, including the 100 amino acid conserved domain and the characteristic CCHC motif. The internal transcribed spacer region-restriction fragment length polymorphism (ITS-RFLP) approach along with intersimple sequence repeat (ISSR) method also differentiated ``race 3'' (F. proliferatum). Races 1 and 2 were identified by unique AFLP patterns. Sequence characterization of race-specific AFLP products revealed significant homologies of these sequences with metabolically important genes.

10aAFLP10aF. oxysporum f. sp ciceris races10agene specific amplification10aISSR10aITS-RFLP10arace delineation10asequence characterization10atranslation elongation factor (EF-1 alpha)1 aGurjar, Gayatri1 aBarve, Maneesha1 aGiri, Ashok, P.1 aGupta, Vidya uhttps://library.ncl.res.in/content/identification-indian-pathogenic-races-fusarium-oxysporum-f-sp-ciceris-gene-specific-its-002008nas a2200253 4500008004100000022001400041245014100055210006900196260007400265300001200339490000800351520105100359653002701410653001501437653002201452653000901474653000901483653003301492653002701525100002101552700002101573700003301594856012701627 2011 eng d a0378-269700aAssociation between chemical and genetic variation in calophyllum inophyllum, a medicinally important tree of the Western Ghats of India0 aAssociation between chemical and genetic variation in calophyllu aSACHSENPLATZ 4-6, PO BOX 89, A-1201 WIEN, AUSTRIAbSPRINGER WIENcAPR a257-2650 v2923 a

The objective of the present work is to study the chemical variation in Calophyllum inophyllum growing along the Western Ghats of India. Contents of dipyranocoumarins (inophyllums) in C. inophyllum were determined to assess whether they could be used as a taxonomic marker for C. inophyllum. This study also aims to establish inter simple sequence repeat (ISSR) markers that can be used to study genetic variation within the species and explore correlation between ISSR and chemical markers. The contents of dipyranocoumarins were estimated in seeds collected from 20 locations. Leaves from plants at the same 20 locations were assayed for ISSR variation. A dendrogram based on Nei's genetic distance as well as principal component analysis based on dipyranocoumarins and ISSR variation clustered plants from these 20 locations into three groups that indicated close relationship among ISSR, dipyranocoumarins contents, and geographical position (variation) of locations. Based on this study, two locations of elite plants were identified.

10aCalophyllum inophyllum10aDendrogram10adipyranocoumarins10aHPLC10aISSR10aPrincipal component analysis10aWestern Ghats of India1 aPawar, Kiran, D.1 aJoshi, Swati, P.1 aThengane, Shubhada, Ratnakar uhttps://library.ncl.res.in/content/association-between-chemical-and-genetic-variation-calophyllum-inophyllum-medicinally-002454nas a2200265 4500008004100000022001400041245010500055210006900160260007400229300001400303490000800317520151000325653002601835653002201861653000901883653001601892653002201908100002401930700001601954700002601970700002401996700002002020700002102040856012702061 2014 eng d a0378-269700aEvaluation of genetic variability in Symplocos laurina Wall. from two biodiversity hotspots of India0 aEvaluation of genetic variability in Symplocos laurina Wall from aSACHSENPLATZ 4-6, PO BOX 89, A-1201 WIEN, AUSTRIAbSPRINGER WIENcDEC a2239-22470 v3003 a

Symplocos laurina Wall., an important medicinal tree species, is one of the pioneering plants for establishment of shola forest ecosystem. We analyzed 208 accessions of S. laurina from 13 populations belonging to three ecoregions in India namely, Western Ghats, Eastern Ghats and Northeast India, to comment on the genetic diversity and population structure of the species. Of the 100 inter simple sequence repeat primers screened, eight were selected based on their clear and reproducible polymorphic patterns. These eight ISSR primers produced on an average 1,014 bands from 208 accessions, of which 6.58 % were rare bands, 55.96 % were shared bands and 37.46 % were similar bands. The primers, UBC835 and UBC880, amplified the highest number of polymorphic loci (16), while the primer UBC852 amplified the least number of amplicons (9). The values for total genetic diversity (H-T) and the average heterozygosity (H-S) were 0.3407 and 0.2263, respectively; while the coefficient of genetic differentiation (G(ST)) was 0.3358. Within-population variance was higher (68 %) than among-population variance (17 %), indicating high intra-population genetic diversity. These populations were grouped according to their geographical location in cluster analysis. Mantel test also showed significant positive correlation between genetic and geographical distances. The present study revealed the importance of the Palghat gap in South India in shaping the distribution of genetic diversity in S. laurina.

10aBiodiversity hotspots10aGenetic diversity10aISSR10aPalghat gap10aSymplocos laurina1 aBhagwat, Rasika, M.1 aBanu, Sofia1 aDholakia, Bhushan, B.1 aKadoo, Narendra, Y.1 aLagu, Meena, D.1 aGupta, Vidya, S. uhttps://library.ncl.res.in/content/evaluation-genetic-variability-symplocos-laurina-wall-two-biodiversity-hotspots-india-003264nas a2200277 4500008004100000022001400041245017200055210006900227260000800296300001200304490000800316520228800324653002402612653001402636653002602650653002602676653000902702653001502711653002202726100002302748700002002771700001902791700002002810700002802830856012802858 2018 eng d a0926-669000aDevelopment of enhanced hypericin yielding transgenic plants and somaclones: high throughput direct organogenesis from leaf and callus explants of Hypericum perforatum0 aDevelopment of enhanced hypericin yielding transgenic plants and cJAN a544-5540 v1113 a

Hypericum perforatum is well known for its anti-depressent properties due to the presence of hypericins and hyperforins. The direct regeneration protocol from leaf explants and Agrobacterium tumefaciens mediated genetic transformation is a prerequisite for gene transfer studies in this valuable plant system as H. perforatum has shown its recalcitrance to these studies previously. The aim of generating transgenic shoots or somaclones in the present study is to select high hypericine yielding H. perforatum plants. High throughput direct bud organogenesis from leaf explants has been achieved for the first time in this plant system on media combination of MS + 5.0 mg/l BAP + 1.0 mg/l. This medium interestingly also worked as the indirect regeneration media for generation of somaclones from callus cultures. Thus far optimized single media can be used for direct and indirect regeneration in H. perforatum. The direct regeneration frequency of plantlets from leaf explants was found to be 80% while 100% was the regeneration frequency noted for indirect plantlet regeneration from callus cultures. The optimized direct regeneration protocol from leaf explants was utilized for A. tumefaciens (harbouring pCAMBIA 1301) mediated genetic transformation studies with the aim of establishing transgenic lines of H. perforatum. The resultant study successfully gave rise to kanamycin resistant GUS positive shoots with transformation efficiency of 3136 +/- 3.6. A total of four transgenic H. perforatum clones namely T2, T3, T5 and T8 with different growth parameters were established, where highest of fivefold increase in hypericin content was recorded by T5 (276.8 +/- 9.2 mu g/g dry wt.) in comparison to control non transformed plants (35.6 +/- 2.7 mu g/g dry wt.). Interestingly the presence of serotonin and melatonin was also detected in transgenic plants on TLC basis. The transgenic nature of the plants was confirmed by PCR with amplification of uidA gene. Apart from it, from indirect regeneration from callus, total of ten somaclones were generated. The ISSR profiling of somaclones scored a total of 156 bands, among which 118 were polymorphic in nature. The glasshouse established soma clones showed up to twofold increase in hypericin content on HPLC analysis.

10aDirect regeneration10aHypericin10aHypericum perforation10aIndirect regeneration10aISSR10aSomaclones10aTransgenic plants1 aKhan, Shamshad, A.1 aVerma, Priyanka1 aArbat, Akshata1 aGaikwad, Sushma1 aParasharami, Varsha, A. uhttps://library.ncl.res.in/content/development-enhanced-hypericin-yielding-transgenic-plants-and-somaclones-high-throughput02332nas a2200217 4500008004100000022001400041245010100055210006900156260000800225300001000233490000700243520161900250653002101869653000901890653002001899653000901919100001901928700002101947700002001968856012601988 2019 eng d a0972-853800aRobust micropropagation protocol for genetically true to type plants of Phule Arakta pomegranate0 aRobust micropropagation protocol for genetically true to type pl cMAR a23-310 v763 a

A rapid and reproducible micropropagation protocol for pomegranate cv. Phule Arakta has been developed using nodal segments of field grown plant. Bud break was induced in basal Woody Plant Medium (WPM) as well as compared when WPM was supplemented with plant growth regulators. Multiple shoot proliferation was induced in the nodal segments on WPM fortified with different concentration of benzyladenine (BAP) where 2mg/I BAP developed maximum number of shoots. Elongation of shoots was further amplified with the addition of adjuvant silver nitrate. Browning of culture medium was controlled by the addition of polyvinylpyrrolidone (PVP) and regular sub-culturing enhanced shoot multiplication as well as elongation. Rooting was induced in the regenerated shoots using Indole-3-butyric acid (IBA) and 3-Indoleacetic acid where best result was obtained using shock treatment with NAA. Sub-culturing resulted in denser and better rooting. The rooted plantlets were further acclimatized and then established in soil. The clonal fidelity of the in vitro grown cultures was assessed using Random Amplified Polymorphic DNA (RAPD) and Inter Simple Sequence Repeats (ISSR) markers. The 10 RAPD decamers produced 55 bands and 4 ISSR produced 19 bands in total. RAPD primers OPC-08, OPC-13 and OPD-07 produced the highest number of distinct bands and ISSR primer UBC-834 produced maximum distinct bands. All the bands were monomorphic which confirms the genetic fidelity of the in-vitro raised P. granatum cv. Phule Arakta and supported the method of mass production of true to type progenies using tissue culture.

10agenetic fidelity10aISSR10aPunica granatum10aRAPD1 aRaman, Taramla1 aGupta, Vidya, S.1 aShukla, Susmita uhttps://library.ncl.res.in/content/robust-micropropagation-protocol-genetically-true-type-plants-phule-arakta-pomegranate