<mets:mets OBJID="eprint_5113" LABEL="Eprints Item" xsi:schemaLocation="http://www.loc.gov/METS/ http://www.loc.gov/standards/mets/mets.xsd http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-3.xsd" xmlns:mets="http://www.loc.gov/METS/" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><mets:metsHdr CREATEDATE="2023-07-05T12:30:44Z"><mets:agent ROLE="CUSTODIAN" TYPE="ORGANIZATION"><mets:name>OAR@ICRISAT</mets:name></mets:agent></mets:metsHdr><mets:dmdSec ID="DMD_eprint_5113_mods"><mets:mdWrap MDTYPE="MODS"><mets:xmlData><mods:titleInfo><mods:title>Culture and regeneration of mesophyll-derived protoplasts of sorghum [Sorghum bicolor (L.) Moench]</mods:title></mods:titleInfo><mods:name type="personal"><mods:namePart type="given">R V</mods:namePart><mods:namePart type="family">Sairam</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">N</mods:namePart><mods:namePart type="family">Seetharama</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">P S</mods:namePart><mods:namePart type="family">Devi</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">A</mods:namePart><mods:namePart type="family">Verma</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:name type="personal"><mods:namePart type="given">U R</mods:namePart><mods:namePart type="family">Murthy</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:abstract>A protocol for plant regeneration from&#13;
mesophyll/protoplasts of sorghum [Sorghum bicolor&#13;
(L.) Moench] was developed. The yield of intact protoplasts,&#13;
their subsequent divisions and regeneration&#13;
were genotype-dependent. The genotype 296B was&#13;
always more responsive than IS 32266. For 296B, the&#13;
sixth leaf from 18-day-old plants kept in dark for 2 days&#13;
before harvesting was found to be the most suitable&#13;
source of viable protoplasts. The first division was&#13;
observed 10–12 days after plating, and the second division&#13;
after 12–14 days. The maximum plating efficiency&#13;
was 4.8% in 296 B, followed by 2.48% in IS 32266.&#13;
Microcolonies were visible after 25–30 days, and microcalli&#13;
after 60–75 days. Whole plants were obtained after&#13;
6–8 weeks of culture of microcalli on MS medium&#13;
containing 0.2 mg l–1 kinetin and 2 mg l–1 BAP. The&#13;
frequency of regeneration in 296B and IS 32266 was&#13;
12.80% and 10.58%, respectively. Ten plants transferred&#13;
to pots in the glasshouse established well. The&#13;
seeds collected from glasshouse-grown plants were&#13;
sown in the field where plants were grown to&#13;
maturity.</mods:abstract><mods:classification authority="lcc">Sorghum</mods:classification><mods:originInfo><mods:dateIssued encoding="iso8061">1999</mods:dateIssued></mods:originInfo><mods:originInfo><mods:publisher>Springer Verlag</mods:publisher></mods:originInfo><mods:genre>Article</mods:genre></mets:xmlData></mets:mdWrap></mets:dmdSec><mets:amdSec ID="TMD_eprint_5113"><mets:rightsMD ID="rights_eprint_5113_mods"><mets:mdWrap MDTYPE="MODS"><mets:xmlData><mods:useAndReproduction>
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