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  <leader>04364nab a2200325 i 4500</leader>
  <controlfield tag="003">BR-BrBNA</controlfield>
  <controlfield tag="005">20240812110640.0</controlfield>
  <controlfield tag="008">240812b2017    bl.qr|pooa||| 00| 0 eng |</controlfield>
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    <subfield code="a">BR-BrBNA</subfield>
    <subfield code="b">eng</subfield>
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  <datafield tag="072" ind1=" " ind2=" ">
    <subfield code="a">F02</subfield>
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  <datafield tag="072" ind1=" " ind2=" ">
    <subfield code="a">F60</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Flores, R.</subfield>
  </datafield>
  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Maldaner, J.</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Brondani, D.</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Cezarotto, V.</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Giacomelli, S.R.</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Garlet, T.M.B.</subfield>
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  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Nicoloso, F.T.</subfield>
  </datafield>
  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Direct and indirect regeneration from Pfaffia tuberosa (Spreng.) Hicken calli and its &#x3B2;-ecdysone production</subfield>
  </datafield>
  <datafield tag="500" ind1=" " ind2=" ">
    <subfield code="a">Publica&#xE7;&#xE3;o on-line; 25 ref.; 1 table; 1 illus.; Summaries (En, Pt)</subfield>
  </datafield>
  <datafield tag="520" ind1=" " ind2=" ">
    <subfield code="a">

ABSTRACT: 

This study aimed to establish calli from nodal segments of P. tuberosa and to
evaluate the effect of plant growth regulators (PGR) on plant regeneration and production of
&#x3B2;-ecdysone from in vitro-grown tissues. Calli were induced from nodal segments on Murashige
and Skoog (MS) basal medium supplemented with 2,4-dichlorophenoxyacetic acid (2,4-D)
combined with N6-benzylaminopurine (BAP). The &#x3B2;-ecdysone concentrations [on a dry weight
(DW) basis] in in vitro grown and field-grown tissues were measured by high performance liquid
chromatography. Direct regenerants (ranging from 4.0 to 75.0%) arose from sprouts present
in the explants only in the medium containing 2,4-D. Maximum frequency of indirect shoot
regeneration from calli (20.0%) was observed in the medium containing 2,4-D and BAP (1.0
&#xB5;M at each). The accumulation of &#x3B2;-ecdysone in the calli was associated with the presence
of shoots and influenced by the concentrations of 2,4-D. Higher amounts of &#x3B2;-ecdysone were
observed in the calli grown with 10.0 &#xB5;M 2,4-D [0.516% (w/w; DW)], whose content was almost
twice that found in the shoots [0.333% (w/w; DW)] from field-grown plants. Calli grown under 1.0
to 5.0 &#xB5;M 2,4-D presented lower &#x3B2;-ecdysone concentrations than those found in the shoot, but
higher than those detected in the roots from field-grown plants [0.022% (w/w; DW)]. Our study
is the first report on the presence of ecdysteroids in the organogenic calli of P. tuberosa, and
may be useful for several biotechnological applications and/or in vitro propagation approaches.

Keywords: In vitro culture, ecdysteroid, Brazilian ginseng, Amaranthaceae.</subfield>
  </datafield>
  <datafield tag="520" ind1=" " ind2=" ">
    <subfield code="a">

RESUMO: 

Regenera&#xE7;&#xE3;o direta e indireta em Pfaffia tuberosa (Spreng.) Hicken e sua
produ&#xE7;&#xE3;o de &#x3B2;-ecdisona. Este estudo teve como objetivo estabelecer calos em P. tuberosa e
avaliar o efeito de reguladores vegetais sobre a regenera&#xE7;&#xE3;o e a produ&#xE7;&#xE3;o de &#x3B2;-ecdisona. Os
calos foram induzidos a partir de segmentos nodais em meio de Murashige e Skoog, acrescido
de 2,4-D e BAP. O teor de &#x3B2;-ecdisona (com base na biomassa seca), nos tecidos in vitro e
em plantas a campo, foi avaliado por cromatografia liquida de alta efici&#xEA;ncia. Observou-se
regenera&#xE7;&#xE3;o direta de brotos (4 a 75%) somente nos explantes cultivados na presen&#xE7;a do
2,4-D. A maior frequ&#xEA;ncia de regenera&#xE7;&#xE3;o indireta a partir dos calos (20%) foi registrada em
meio com 2,4-D e BAP (1 &#xB5;M de cada). O teor de &#x3B2;-ecdisona nos calos foi associado com
a presen&#xE7;a de brotos e influenciado pelas concentra&#xE7;&#xF5;es de 2,4-D. Maiores quantidades de
&#x3B2;-ecdisona foram observadas nos calos cultivados com 10 &#xB5;M de 2,4-D (0,516%), cujo teor foi
quase duas vezes maior que o encontrado nos brotos (0,333%) das plantas a campo. Calos
cultivados com concentra&#xE7;&#xF5;es de 1 a 5 &#xB5;M de 2,4-D apresentaram menores teores de &#x3B2;-ecdisona
quando comparado com aqueles encontrados nos brotos, mas maiores que o detectado nas
ra&#xED;zes (0,022%) das plantas a campo. Este &#xE9; o primeiro estudo que mostra a presen&#xE7;a de
ecdister&#xF3;ides em calos organog&#xEA;nicos de P. tuberosa.

Palavras-chave: cultivo in vitro, ecdister&#xF3;ides, ginseng brasileiro, Amaranthaceae.</subfield>
  </datafield>
  <datafield tag="650" ind1=" " ind2=" ">
    <subfield code="a">CULTIVO IN VITRO</subfield>
  </datafield>
  <datafield tag="650" ind1=" " ind2=" ">
    <subfield code="a">PLANTA MEDICINAL</subfield>
  </datafield>
  <datafield tag="650" ind1=" " ind2=" ">
    <subfield code="a">AMARANTHACEAE</subfield>
  </datafield>
  <datafield tag="773" ind1="0" ind2=" ">
    <subfield code="0">3543</subfield>
    <subfield code="9">317119</subfield>
    <subfield code="d">Botucatu-SP Instituto de Bioci&#xEA;ncias - Departamento de Qu&#xED;mica e Bioqu&#xED;mica 1998</subfield>
    <subfield code="o">2024-3719</subfield>
    <subfield code="t">Revista Brasileira de Plantas Medicinais (Brazil)</subfield>
    <subfield code="x">1516-0572</subfield>
    <subfield code="g">v. 19(2) p. 266-273; (2017)</subfield>
    <subfield code="w">BR2024002111</subfield>
  </datafield>
  <datafield tag="856" ind1=" " ind2=" ">
    <subfield code="u">https://www.sbpmed.org.br/admin/files/papers/file_EZHABDH1EQYU.pdf</subfield>
  </datafield>
  <datafield tag="942" ind1=" " ind2=" ">
    <subfield code="c">Anal&#xED;tica</subfield>
  </datafield>
  <datafield tag="999" ind1=" " ind2=" ">
    <subfield code="c">300837</subfield>
    <subfield code="d">300837</subfield>
  </datafield>
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