Annona Species Monograph.pdf - Crops for the Future
Annona Species Monograph.pdf - Crops for the Future
Annona Species Monograph.pdf - Crops for the Future
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Chapter 9. Genetic Improvement<br />
9.5 Role of modern biotechnology<br />
9.5.1 Tissue culture<br />
Tissue culture has many uses: a) micropropagation; b) maintenance of<br />
germplasm collections; c) embryo rescue; d) development of haploid plants;<br />
e) enhancement of variability by somaclonal variation; and f) to prepare<br />
explants <strong>for</strong> trans<strong>for</strong>mation methods (Encina et al., 1999; Herrera, 1999).<br />
However, <strong>for</strong> most annona work <strong>the</strong> main objective is micropropagation, as<br />
<strong>the</strong> conventional methods of propagation are slow and costly, and in some<br />
cases, such as with cherimoya, are also inefficient. This appears to be<br />
because <strong>the</strong> morphological potential <strong>for</strong> rooting of cherimoya is very low<br />
(Encina et al., 1999).<br />
Researchers have successfully micropropagated cherimoya, sugar apple,<br />
soursop and atemoya. Atemoya clonal propagation was described by Rasai et<br />
al. (1994). They obtained multiple shoot <strong>for</strong>mation from hypocotyls and<br />
nodal cuttings of <strong>the</strong> cultivar ‘African Pride’. The explants were cultivated in<br />
MS medium supplemented with BAP, kinetin, biotin and calcium<br />
panto<strong>the</strong>nate. In spite of improved rooting by shoot pre-treatment in liquid<br />
MS medium containing IBA, <strong>the</strong> percentage of rooting was still low (40%)<br />
and remains a limiting factor <strong>for</strong> commercial micropropagation of atemoya.<br />
Benjoy and Hariharam (1992) described plantlet differentiation in soursop.<br />
They found a mean of 4.8 shoots per hypocotyl explant growing in an MS<br />
medium containing BAP and NAA. However, <strong>the</strong>y reported only relative<br />
success in rooting and survival (35%). To improve <strong>the</strong> system, Lemos and<br />
Baker (1998) suggested <strong>the</strong> use of sorbitol to induce de novo shoot<br />
development and Lemos and Blake (1996 c) tried galactose and NAA to<br />
stimulate rooting. None<strong>the</strong>less, no commercial protocol is ready <strong>for</strong> use.<br />
The first haploid plants induced by an<strong>the</strong>r culture in fruit trees were reported<br />
by Nair et al. (1983) with sugar apple. The availability of haploids is very<br />
important <strong>for</strong> fruit-breeding, because of <strong>the</strong> long generation intervals, <strong>the</strong><br />
highly heterozygous nature of most fruit species and <strong>the</strong> presence of<br />
par<strong>the</strong>nocarpy and self-incompatibility. These researchers obtained callus<br />
differentiation, and <strong>for</strong>mation of triploid roots and shoots from sugar apple<br />
endosperm (Nair et al., 1986). Their aim was development of seedless fruits,<br />
but a complete plantlet was not obtained.<br />
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