[HTML][HTML] Efficient micropropagation protocol and genome size estimation of an important cover crop, Mucuna bracteata DC. ex Kurz
Mucuna bracteata DC. ex Kurz is an important cover crop in plantations across the tropics.
However, low germination rate and poor viability of Mucuna seeds pose significant
challenges of using the seeds as starting material. To address these limitations, we have
optimized seed germination conditions (such as scarification period, surface sterilization
protocols and imbibition period) and in vitro propagation protocols for M. bracteata. We
found that seeds treated with sulphuric acid for 30 min, imbibed for 6 h and incubated in dark …
However, low germination rate and poor viability of Mucuna seeds pose significant
challenges of using the seeds as starting material. To address these limitations, we have
optimized seed germination conditions (such as scarification period, surface sterilization
protocols and imbibition period) and in vitro propagation protocols for M. bracteata. We
found that seeds treated with sulphuric acid for 30 min, imbibed for 6 h and incubated in dark …
Efficient micropropagation protocol and genome size estimation of an important cover crop, Mucuna bracteata DC. ex Kurz.
NAA Nazrin Abd Aziz, TBC Tan BoonChin… - 2018 - cabidigitallibrary.org
Mucuna bracteata DC. ex Kurz is an important cover crop in plantations across the tropics.
However, low germination rate and poor viability of Mucuna seeds pose significant
challenges of using the seeds as starting material. To address these limitations, we have
optimized seed germination conditions (such as scarification period, surface sterilization
protocols and imbibition period) and in vitro propagation protocols for M. bracteata. We
found that seeds treated with sulphuric acid for 30 min, imbibed for 6 h and incubated in dark …
However, low germination rate and poor viability of Mucuna seeds pose significant
challenges of using the seeds as starting material. To address these limitations, we have
optimized seed germination conditions (such as scarification period, surface sterilization
protocols and imbibition period) and in vitro propagation protocols for M. bracteata. We
found that seeds treated with sulphuric acid for 30 min, imbibed for 6 h and incubated in dark …
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