Callus induction and organogenesis in Dioscorea species

Hitherto, there is little {nformation on species or line and organ specificity concerning callus and organ formation, plant regeneration from calli and proliferation from explants in yam species. To address, we examined variation in species/organ specificity for callus induction and organogenesis us...

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Veröffentlicht in:Ikushugaku zasshi 1991/12/01, Vol.41(4), pp.561-569
Hauptverfasser: Belarmino, M.M. (University of the Philippines, Los Banos, Laguna (Philippines)), Rosario, A.G
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creator Belarmino, M.M. (University of the Philippines, Los Banos, Laguna (Philippines))
Rosario, A.G
description Hitherto, there is little {nformation on species or line and organ specificity concerning callus and organ formation, plant regeneration from calli and proliferation from explants in yam species. To address, we examined variation in species/organ specificity for callus induction and organogenesis using three yam species, i.e. Dioscorea esculenta BURK., D. rotun.data POIR. and D. alata L. Axillary buds or shoot tips and single-node segments with one or two axillary buds were inoculated onto the culture media containing various combinations of plant hormones. Using axillary buds, D. esculenta acc. LE 030 produced calli on MS medium containing 2.0mg/l NAA in combination with 0.0, 0.2 and 0.5mg/l BA followed by green spot (45 to 75%), shoot (20 fo 30%) and root (20 to 90%) formation from calli. Similarly, D. alata L. cv. Farm Lisbon produced calli only on MS medium containing 1.0mg/l BA and 2.0mg/l NAA followed by high green spot (75%), shoot (50%) and root (10%) formation from the calli. On the other hand, two accessions of D, rotundata i.e. HR 018 and 020 produced calli followed by green spot (13 to 100%) and root (15 to 85%), but no shoot formatlon from the calli. Using single-node segments, two accessions of D. esculenta produced shoots at an average of 2.8 directly from nodal explant without callus formation on MS medium containing 0.1 mg/l NAA and 0.2 mg/l BA. Similarly, two accessions of D. rotundata produced shoots at an average of 3.2 to 4.8 on MS medium containing 1.0 to 2.0mg/l and 0.2 to 2.0mg/l BA. However, two cultlvars of D. alata and two accessions of D. rotuudata produced at an average of 4.0 and 6.0 shoots, respectively through the proliferation of bud on MS medium containing 15.0mg/l adenine sulfate. This proliferation was not affected by the additlon of NAAat 0.1, 0.5 and 1.0mg/l NAA. The present experiment showed species or line and organ specificity for callus and organ formation and plant regeneration from calli and direct proliferation from axillary buds. Particularly, It is important that D. alata with poor seed formatlon regenerated plants from calli and also directly from single-node segment through the proliferation of axillary buds.
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(University of the Philippines, Los Banos, Laguna (Philippines)) ; Rosario, A.G</creator><creatorcontrib>Belarmino, M.M. (University of the Philippines, Los Banos, Laguna (Philippines)) ; Rosario, A.G</creatorcontrib><description>Hitherto, there is little {nformation on species or line and organ specificity concerning callus and organ formation, plant regeneration from calli and proliferation from explants in yam species. To address, we examined variation in species/organ specificity for callus induction and organogenesis using three yam species, i.e. Dioscorea esculenta BURK., D. rotun.data POIR. and D. alata L. Axillary buds or shoot tips and single-node segments with one or two axillary buds were inoculated onto the culture media containing various combinations of plant hormones. Using axillary buds, D. esculenta acc. LE 030 produced calli on MS medium containing 2.0mg/l NAA in combination with 0.0, 0.2 and 0.5mg/l BA followed by green spot (45 to 75%), shoot (20 fo 30%) and root (20 to 90%) formation from calli. Similarly, D. alata L. cv. Farm Lisbon produced calli only on MS medium containing 1.0mg/l BA and 2.0mg/l NAA followed by high green spot (75%), shoot (50%) and root (10%) formation from the calli. On the other hand, two accessions of D, rotundata i.e. HR 018 and 020 produced calli followed by green spot (13 to 100%) and root (15 to 85%), but no shoot formatlon from the calli. Using single-node segments, two accessions of D. esculenta produced shoots at an average of 2.8 directly from nodal explant without callus formation on MS medium containing 0.1 mg/l NAA and 0.2 mg/l BA. Similarly, two accessions of D. rotundata produced shoots at an average of 3.2 to 4.8 on MS medium containing 1.0 to 2.0mg/l and 0.2 to 2.0mg/l BA. 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(University of the Philippines, Los Banos, Laguna (Philippines))</creatorcontrib><creatorcontrib>Rosario, A.G</creatorcontrib><title>Callus induction and organogenesis in Dioscorea species</title><title>Ikushugaku zasshi</title><addtitle>Jpn.J. Breed.</addtitle><description>Hitherto, there is little {nformation on species or line and organ specificity concerning callus and organ formation, plant regeneration from calli and proliferation from explants in yam species. To address, we examined variation in species/organ specificity for callus induction and organogenesis using three yam species, i.e. Dioscorea esculenta BURK., D. rotun.data POIR. and D. alata L. Axillary buds or shoot tips and single-node segments with one or two axillary buds were inoculated onto the culture media containing various combinations of plant hormones. Using axillary buds, D. esculenta acc. LE 030 produced calli on MS medium containing 2.0mg/l NAA in combination with 0.0, 0.2 and 0.5mg/l BA followed by green spot (45 to 75%), shoot (20 fo 30%) and root (20 to 90%) formation from calli. Similarly, D. alata L. cv. Farm Lisbon produced calli only on MS medium containing 1.0mg/l BA and 2.0mg/l NAA followed by high green spot (75%), shoot (50%) and root (10%) formation from the calli. On the other hand, two accessions of D, rotundata i.e. HR 018 and 020 produced calli followed by green spot (13 to 100%) and root (15 to 85%), but no shoot formatlon from the calli. Using single-node segments, two accessions of D. esculenta produced shoots at an average of 2.8 directly from nodal explant without callus formation on MS medium containing 0.1 mg/l NAA and 0.2 mg/l BA. Similarly, two accessions of D. rotundata produced shoots at an average of 3.2 to 4.8 on MS medium containing 1.0 to 2.0mg/l and 0.2 to 2.0mg/l BA. However, two cultlvars of D. alata and two accessions of D. rotuudata produced at an average of 4.0 and 6.0 shoots, respectively through the proliferation of bud on MS medium containing 15.0mg/l adenine sulfate. This proliferation was not affected by the additlon of NAAat 0.1, 0.5 and 1.0mg/l NAA. The present experiment showed species or line and organ specificity for callus and organ formation and plant regeneration from calli and direct proliferation from axillary buds. Particularly, It is important that D. alata with poor seed formatlon regenerated plants from calli and also directly from single-node segment through the proliferation of axillary buds.</description><subject>6-BENZILADENINA</subject><subject>6-BENZYLADENINE</subject><subject>ACIDE NAPHTALENE ACETIQUE</subject><subject>ACIDO NAFTILACETICO</subject><subject>ADENINA</subject><subject>ADENINE</subject><subject>Agronomy. 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Soil science and plant productions</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>CAL</topic><topic>CALLO</topic><topic>CALLUS</topic><topic>CULTURE MEDIA</topic><topic>DIOSCOREA</topic><topic>EXPLANT</topic><topic>EXPLANTES</topic><topic>EXPLANTS</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetics and breeding of economic plants</topic><topic>Haploidy, in vitro culture applications, somatic hybrids</topic><topic>MEDIO DE CULTIVO</topic><topic>MILIEU DE CULTURE</topic><topic>NAA</topic><topic>ORGANOGENESE</topic><topic>ORGANOGENESIS</topic><topic>Plant breeding: fundamental aspects and methodology</topic><topic>Yam,Dioscorea. Organogenesis,NAA,BA,adenlne sulfate</topic><toplevel>online_resources</toplevel><creatorcontrib>Belarmino, M.M. 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Breed.</addtitle><date>1991-12-01</date><risdate>1991</risdate><volume>41</volume><issue>4</issue><spage>561</spage><epage>569</epage><pages>561-569</pages><issn>0536-3683</issn><eissn>2185-291X</eissn><coden>IKZAAD</coden><abstract>Hitherto, there is little {nformation on species or line and organ specificity concerning callus and organ formation, plant regeneration from calli and proliferation from explants in yam species. To address, we examined variation in species/organ specificity for callus induction and organogenesis using three yam species, i.e. Dioscorea esculenta BURK., D. rotun.data POIR. and D. alata L. Axillary buds or shoot tips and single-node segments with one or two axillary buds were inoculated onto the culture media containing various combinations of plant hormones. Using axillary buds, D. esculenta acc. LE 030 produced calli on MS medium containing 2.0mg/l NAA in combination with 0.0, 0.2 and 0.5mg/l BA followed by green spot (45 to 75%), shoot (20 fo 30%) and root (20 to 90%) formation from calli. Similarly, D. alata L. cv. Farm Lisbon produced calli only on MS medium containing 1.0mg/l BA and 2.0mg/l NAA followed by high green spot (75%), shoot (50%) and root (10%) formation from the calli. On the other hand, two accessions of D, rotundata i.e. HR 018 and 020 produced calli followed by green spot (13 to 100%) and root (15 to 85%), but no shoot formatlon from the calli. Using single-node segments, two accessions of D. esculenta produced shoots at an average of 2.8 directly from nodal explant without callus formation on MS medium containing 0.1 mg/l NAA and 0.2 mg/l BA. Similarly, two accessions of D. rotundata produced shoots at an average of 3.2 to 4.8 on MS medium containing 1.0 to 2.0mg/l and 0.2 to 2.0mg/l BA. However, two cultlvars of D. alata and two accessions of D. rotuudata produced at an average of 4.0 and 6.0 shoots, respectively through the proliferation of bud on MS medium containing 15.0mg/l adenine sulfate. This proliferation was not affected by the additlon of NAAat 0.1, 0.5 and 1.0mg/l NAA. The present experiment showed species or line and organ specificity for callus and organ formation and plant regeneration from calli and direct proliferation from axillary buds. Particularly, It is important that D. alata with poor seed formatlon regenerated plants from calli and also directly from single-node segment through the proliferation of axillary buds.</abstract><cop>Tokyo</cop><pub>Japanese Society of Breeding</pub><doi>10.1270/jsbbs1951.41.561</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects 6-BENZILADENINA
6-BENZYLADENINE
ACIDE NAPHTALENE ACETIQUE
ACIDO NAFTILACETICO
ADENINA
ADENINE
Agronomy. Soil science and plant productions
Biological and medical sciences
Biotechnology
CAL
CALLO
CALLUS
CULTURE MEDIA
DIOSCOREA
EXPLANT
EXPLANTES
EXPLANTS
Fundamental and applied biological sciences. Psychology
Genetics and breeding of economic plants
Haploidy, in vitro culture applications, somatic hybrids
MEDIO DE CULTIVO
MILIEU DE CULTURE
NAA
ORGANOGENESE
ORGANOGENESIS
Plant breeding: fundamental aspects and methodology
Yam,Dioscorea. Organogenesis,NAA,BA,adenlne sulfate
title Callus induction and organogenesis in Dioscorea species
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