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	<front>
		<journal-meta>
			<journal-id journal-id-type="publisher-id">pnut</journal-id>
			<journal-id journal-id-type="allenpress-id">pnut</journal-id>
			<journal-title>Peanut Science</journal-title>
			<issn pub-type="ppub">0095-3679</issn>
			<issn pub-type="active">0095-3679</issn>
			<publisher>
				<publisher-name>American Peanut Research and Education Society</publisher-name>
			</publisher>
		</journal-meta>
		<article-meta>
			<article-id pub-id-type="doi">10.3146/i0095-3679-23-2-1</article-id>
			<article-categories>
				<subj-group subj-group-type="heading">
					<subject>Articles</subject>
				</subj-group>
			</article-categories>
			<title-group>
				<article-title>High Efficiency Peanut Regeneration Using a Nonimbibed Immature Leaflet Culture Method</article-title>
			</title-group>
			<contrib-group>
				<contrib contrib-type="author" xlink:type="simple">
					<name name-style="western">
						<given-names>S. D.</given-names><x xml:space="preserve"> </x>
						<surname>Utomo</surname>
					</name>
					<xref ref-type="aff" rid="aff1"><sup>1</sup></xref><x xml:space="preserve">, </x>
				</contrib>
				<contrib contrib-type="author" xlink:type="simple">
					<name name-style="western">
						<given-names>A. K.</given-names><x xml:space="preserve"> </x>
						<surname>Weissinger</surname>
					</name>
					<xref ref-type="aff" rid="aff2"><sup>2</sup></xref><x xml:space="preserve">, and </x>
				</contrib>
				<contrib contrib-type="author" xlink:type="simple">
					<name name-style="western">
						<given-names>T. G.</given-names><x xml:space="preserve"> </x>
						<surname>Isleib</surname>
					</name>
					<xref ref-type="corresp" rid="cor1">&ast;<sup>,</sup></xref>
					<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
				</contrib>
				
					<aff id="aff1">
					<label><sup>1</sup></label> Dept. of Agronomy, College of Agric., Lampung Univ., Jl. S. Brodjonegoro 1 Bandar Lampung 35145, Indonesia.
				</aff>
				
					<aff id="aff2">
					<label><sup>2</sup></label> Dept. of Crop Science, N.C. State Univ., Box 7629, Raleigh, NC 27695-7629.
				</aff>
			</contrib-group>
			<author-notes>
				<corresp id="cor1">&ast;Corresponding author.</corresp>
			</author-notes>
			<pub-date pub-type="ppub">
				<month>7</month>
				<year>1996</year>
			</pub-date>
			<volume>23</volume>
			<issue>2</issue>
			<fpage>71</fpage>
			<lpage>75</lpage>
			<permissions>
				<copyright-statement>American Peanut Research and Education Society</copyright-statement>
				<copyright-year>1996</copyright-year>
				<copyright-holder>American Peanut Research and Education Society</copyright-holder>
			</permissions>
			<related-article related-article-type="pdf" xlink:href="i0095-3679-23-2-1.pdf" xlink:type="simple"></related-article>
			<abstract>
				<title>Abstract</title>
				<p>Efficient plant regeneration is an essential part of gene transfer systems using recombinant DNA technology. Efficiency of regeneration from immature leaflets of peanut (<italic>Arachis hypogaea</italic> L.) was compared among several explant treatments in an effort to maximize recovery of plants from culture. In one experiment, explants were derived from leaflets of cv. NC 7 from dry mature seeds or from mature seeds which had been imbibed for 1 or 4 d. To avoid confounding treatment effects with variation among individual seeds, both nonimbibed and imbibed leaflets originated from a single seed. For each seed, four nonimbibed leaflets from a single leaf were excised, sterilized, rinsed, and plated on MS-based medium amended with 4 mg L<sup>-1</sup> benzylaminopurine and 2 mg L<sup>-1</sup> naphthaleneacetic acid. The embryonic axis with the other leaf (four remaining leaflets) and one cotyledon attached was then imbibed in water for 1 or 4 d. After 4 wk in culture, 53&percnt; of nonimbibed leaflets, 37&percnt; of leaflets imbibed for 1 d, and 6&percnt; of leaflets imbibed for 4 d produced shoots. Subsequently, regeneration efficiency was compared among immature leaflet cultures from nonimbibed seeds of four cultivars representing three botanical varieties from two subspecies. Shoot frequency after 4 wk in culture averaged 9&percnt; for Peruvian introduction A<sub>2</sub> (NC Ac 17090) representing subsp. <italic>fastigiata</italic> var. <italic>peruviana</italic> versus 53&percnt; for cv. NC 7 and Bolivian introduction B<sub>2</sub> (PI 274191), both representing subsp. <italic>hypogaea</italic> var. <italic>hypogaea.</italic> At 6 wk after plating, these frequencies increased to 28 and 61&percnt;, respectively. The response of Argentine introduction C<sub>2</sub> (PI 262000) representing subsp. <italic>fastigiata</italic> var. <italic>vulgaris</italic> was intermediate to vars. <italic>hypogaea</italic> and <italic>fastigiata.</italic> Shoot proliferation in var. <italic>hypogaea</italic> was significantly greater than in the other varieties, whereas it was significantly lower in var. <italic>peruviana.</italic> Regenerated plants developed normal flowers and pods in the greenhouse. The study indicated that <italic>A. hypogaea</italic> can be cultured efficiently from nonimbibed leaflets.</p>
			</abstract>
			<kwd-group>
				<title>Key Words</title>
				<kwd><italic>Arachis hypogaea</italic> L</kwd><x xml:space="preserve">; </x><x xml:space="preserve">, </x>
				<kwd>tissue culture</kwd><x xml:space="preserve">; </x><x xml:space="preserve">, </x>
				<kwd>imbibition</kwd>
			</kwd-group>
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				<page-count count="5"></page-count>
			</counts>
		</article-meta>
	</front>
</article>
