TY - JOUR
T1 - Multispectral phloem-mobile probes
T2 - Properties and applications
AU - Knoblauch, Michael
AU - Vendrell, Marc
AU - De Leau, Erica
AU - Paterlini, Andrea
AU - Knox, Kirsten
AU - Ross-Elliot, Tim
AU - Reinders, Anke
AU - Brockman, Stephen A.
AU - Ward, John
AU - Oparka, Karl
N1 - Publisher Copyright:
© 2014 American Society of Plant Biologists. All rights reserved.
PY - 2015/4/1
Y1 - 2015/4/1
N2 - Using Arabidopsis (Arabidopsis thaliana) seedlings, we identified a range of small fluorescent probes that entered the translocation stream and were unloaded at the root tip. These probes had absorbance/emission maxima ranging from 367/454 to 546/576 nm and represent a versatile toolbox for studying phloem transport. Of the probes that we tested, naturally occurring fluorescent coumarin glucosides (esculin and fraxin) were phloem loaded and transported in oocytes by the sucrose transporter, AtSUC2. Arabidopsis plants in which AtSUC2 was replaced with barley (Hordeum vulgare) sucrose transporter (HvSUT1), which does not transport esculin in oocytes, failed to load esculin into the phloem. In wild-type plants, the fluorescence of esculin decayed to background levels about 2 h after phloem unloading, making it a suitable tracer for pulse-labeling studies of phloem transport. We identified additional probes, such as carboxytetraethylrhodamine, a red fluorescent probe that, unlike esculin, was stable for several hours after phloem unloading and could be used to study phloem transport in Arabidopsis lines expressing green fluorescent protein.
AB - Using Arabidopsis (Arabidopsis thaliana) seedlings, we identified a range of small fluorescent probes that entered the translocation stream and were unloaded at the root tip. These probes had absorbance/emission maxima ranging from 367/454 to 546/576 nm and represent a versatile toolbox for studying phloem transport. Of the probes that we tested, naturally occurring fluorescent coumarin glucosides (esculin and fraxin) were phloem loaded and transported in oocytes by the sucrose transporter, AtSUC2. Arabidopsis plants in which AtSUC2 was replaced with barley (Hordeum vulgare) sucrose transporter (HvSUT1), which does not transport esculin in oocytes, failed to load esculin into the phloem. In wild-type plants, the fluorescence of esculin decayed to background levels about 2 h after phloem unloading, making it a suitable tracer for pulse-labeling studies of phloem transport. We identified additional probes, such as carboxytetraethylrhodamine, a red fluorescent probe that, unlike esculin, was stable for several hours after phloem unloading and could be used to study phloem transport in Arabidopsis lines expressing green fluorescent protein.
UR - http://www.scopus.com/inward/record.url?scp=84926147000&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84926147000&partnerID=8YFLogxK
U2 - 10.1104/pp.114.255414
DO - 10.1104/pp.114.255414
M3 - Article
C2 - 25653316
AN - SCOPUS:84926147000
SN - 0032-0889
VL - 167
SP - 1211
EP - 1220
JO - Plant physiology
JF - Plant physiology
IS - 4
ER -