2014
DOI: 10.1016/j.molcatb.2013.07.013
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Establishment of an ex vivo laticifer cell suspension culture from Taraxacum brevicorniculatum as a production system for cis-isoprene

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Cited by 9 publications
(3 citation statements)
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“…However, at present, these experiments are restricted to Hevea brasiliensis , although it is expected that they can be applied in the future to T. kok‐saghyz and its close relative T. brevicorniculatum . Currently, many of the proteins and molecular pathways involved in rubber biosynthesis are known (Hillebrand et al, ; Post et al, ; Schmidt et al, ; Wahler et al, ). It was shown that rubber from T. kok‐saghyz contains less protein than rubber from H. brasiliensis , which might cause fewer allergic reactions (Van Beilen & Poirier, ).…”
Section: Cultivation Of Plants Of the Genus Taraxacummentioning
confidence: 99%
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“…However, at present, these experiments are restricted to Hevea brasiliensis , although it is expected that they can be applied in the future to T. kok‐saghyz and its close relative T. brevicorniculatum . Currently, many of the proteins and molecular pathways involved in rubber biosynthesis are known (Hillebrand et al, ; Post et al, ; Schmidt et al, ; Wahler et al, ). It was shown that rubber from T. kok‐saghyz contains less protein than rubber from H. brasiliensis , which might cause fewer allergic reactions (Van Beilen & Poirier, ).…”
Section: Cultivation Of Plants Of the Genus Taraxacummentioning
confidence: 99%
“…It is also possible to cultivate roots in a sterile environment controlling the growth conditions without phytohormones. Another possibility is to cultivate only the rubber‐producing laticifer cells in vitro; this has been tried as proof of concept but not at a larger scale (Post et al, ).…”
Section: Cultivation Of Plants Of the Genus Taraxacummentioning
confidence: 99%
“…The overexpression constructs for NtFT5 G170W and NtFT5 MM W170G were prepared by digesting the NtFT5 G170W and NtFT5 MM W170G amplicons (generated using the primers listed in Supplementary Table S1) with the appropriate restriction enzymes and inserting them into vector pRT104, containing the CaMV 35S promoter and terminator (Töpfer et al ., 1987). The entire expression cassette was then excised with HindIII and transferred to vector plab12.10 (Post et al ., 2014).…”
Section: Methodsmentioning
confidence: 99%