Isolation of root hairs from seedlings of Pisum sativum. Identification of root hair specific proteins by in situ labeling

1987 ◽  
Vol 69 (1) ◽  
pp. 129-136 ◽  
Author(s):  
Mechthild Rohm ◽  
Dietrich Werner
1991 ◽  
Vol 39 (4) ◽  
pp. 435-440 ◽  
Author(s):  
M J Bodson ◽  
W H Outlaw ◽  
S H Silvers

Malate, which plays many essential roles in plant metabolism, is a potent in vitro inhibitor of the cytosolic enzyme phosphoenolpyruvate carboxylase (PEPC). Because PEPC activity leads to malate biosynthesis, malate is assumed to attenuate its own synthesis in situ. To test this hypothesis, we measured directly the malate content of picoliter samples of Raphanus root-hair cytoplasm using quantitative histochemical techniques. We also obtained an estimate for malate accumulation in these cells. These values were compared with the PEPC activity of individual root hairs (less than 2 ng). The results indicate that high cytoplasmic malate concentration does not severely inhibit PEPC in situ. We suggest that the focus for studies on the regulation of organic anion accumulation be on the interactive effects of malate and other PEPC effectors.


2000 ◽  
Vol 80 (4) ◽  
pp. 801-804 ◽  
Author(s):  
Robert H. Gulden ◽  
J. Kevin Vessey

Under three levels of phosphorus availability, inoculation of pea plants with Penicillium bilaii in growth pouches had no effect on root length (excluding root hairs), mean root diameter, root-hair diameter, P accumulation or shoot growth. However, inoculation with P. bilaii resulted in a 22% increase in the proportion of root containing root hairs and a 33% increase in the mean root-hair length. Key words: Pea, Penicillium bilaii, Pisum sativum, phosphorus, root hairs, root morphology


1987 ◽  
Vol 42 (5) ◽  
pp. 537-541 ◽  
Author(s):  
Dietrich Werner ◽  
Andreas Bernd Wolff

Abstract In root hairs from seedlings of Glycine max cultivars, isolated from the root system and com­ pared with the complete organ, specific soluble proteins have been found. By FPLC chromatography and SDS gel electrophoresis root hair specific proteins with molecular weights of 13, 21, 34, 38 and 42 kDa were separated. Additionally, proteins with molecular weights of 12, 20, 69 and 74 kDa were significantly enriched in root hairs compared to roots without root hairs. By using CNBr activated Sepharose with antibodies against the root system without root hairs, the pres­ ence of root hair specific proteins was confirmed in extracts from isolated root hair cells. Enrichment of Fe and Ca in some of the proteins from the root hairs is demonstrated. The present knowledge of the biochemical specificity of legume root hairs, the target cells of Rhizobium and Bradyrhizobium infection, is discussed.


Author(s):  
K.S. Walters ◽  
R.D. Sjolund ◽  
K.C. Moore

Callose, B-1,3-glucan, a component of cell walls, is associated with phloem sieve plates, plasmodesmata, and other cell wall structures that are formed in response to wounding or infection. Callose reacts with aniline blue to form a fluorescent complex that can be recognized in the light microscope with ultraviolet illumination. We have identified callose in cell wall protuberances that are formed spontaneously in suspension-cultured cells of S. tortuosus and in the tips of root hairs formed in sterile callus cultures of S. tortuosus. Callose deposits in root hairs are restricted to root hair tips which appear to be damaged or deformed, while normal root hair tips lack callose deposits. The callose deposits found in suspension culture cells are restricted to regions where unusual outgrowths or protuberances are formed on the cell surfaces, specifically regions that are the sites of new cell wall formation.Callose formation has been shown to be regulated by intracellular calcium levels.


Plants ◽  
2021 ◽  
Vol 10 (1) ◽  
pp. 150 ◽  
Author(s):  
Katarzyna Retzer ◽  
Wolfram Weckwerth

Plant growth and productivity are orchestrated by a network of signaling cascades involved in balancing responses to perceived environmental changes with resource availability. Vascular plants are divided into the shoot, an aboveground organ where sugar is synthesized, and the underground located root. Continuous growth requires the generation of energy in the form of carbohydrates in the leaves upon photosynthesis and uptake of nutrients and water through root hairs. Root hair outgrowth depends on the overall condition of the plant and its energy level must be high enough to maintain root growth. TARGET OF RAPAMYCIN (TOR)-mediated signaling cascades serve as a hub to evaluate which resources are needed to respond to external stimuli and which are available to maintain proper plant adaptation. Root hair growth further requires appropriate distribution of the phytohormone auxin, which primes root hair cell fate and triggers root hair elongation. Auxin is transported in an active, directed manner by a plasma membrane located carrier. The auxin efflux carrier PIN-FORMED 2 is necessary to transport auxin to root hair cells, followed by subcellular rearrangements involved in root hair outgrowth. This review presents an overview of events upstream and downstream of PIN2 action, which are involved in root hair growth control.


1986 ◽  
Vol 64 (10) ◽  
pp. 2216-2226 ◽  
Author(s):  
Yves Prin ◽  
Mireille Rougier

The aim of the present study was to investigate the Alnus root surface using seedlings grown axenically. This study has focused on root zones where infection by the symbiotic actinomycete Frankia takes place. The zones examined extend from the root cap to the emerging root hair zone. The root cap ensheaths the Alnus root apex and extends over the root surface as a layer of highly flattened cells closely appressed to the root epidermal cell wall. These cells contain phenolic compounds as demonstrated by various histochemical tests. They are externally bordered by a thin cell wall coated by a thin mucilage layer. The root cap is ruptured when underlying epidermal cells elongate, and cell remnants are still found in the emerging root hair zone. Young emerging root hairs are bordered externally by a cell wall covered by a thin mucilage layer which reacts positively to the tests used for the detection of polysaccharides, glycoproteins, and anionic sites. The characteristics of the Alnus root surface and the biological function of mucilage and phenols present at the root surface are discussed in relation to the infection process.


Resting spore germination and the root hair stages of the life history of Plasmodiophora brassicae were studied in stained preparations of infected Brassica rapa seedling roots. Naked protoplasts, usually possessing two unequal flagella, were released from resting spores through a small circular pore. They penetrated the root hairs of B. rapa and there developed into plasmodia which, after becoming multinucleate, cleaved to form zoosporangia con­taining incipient zoospores. Biflagellate zoospores were released from root hair zoosporangia and fused in pairs, although karyogamy did not occur. The resulting binucleate zoospores infected the cortical dells of B. rapa to form binucleate plasmodia, the earliest stages of the secondary phase of the life history. These findings are discussed in relation to previous studies on the life history of P. brassicae in Brassica plants and in Brassica tissue cultures, and a new complete life history, including nuclear fusion in the secondary plasmodium, is suggested for the organism.


1983 ◽  
Vol 61 (11) ◽  
pp. 2863-2876 ◽  
Author(s):  
Alison M. Berry ◽  
John G. Torrey

Structural and cell developmental studies of root hair deformation in Alnus rubra Bong. (Betulaceae) were carried out following inoculation with the soil pseudomonad Pseudomonas cepacia 85, alone or in concert with Frankia, and using axenically grown seedlings. Deformational changes can be observed in elongating root hairs within 2 h of inoculation with P. cepacia 85. These growing root hairs become branched or multilobed and highly modified from the single-tip growth of axenic root hairs. The cell walls of deformed hairs are histologically distinctive when stained with the fluorochrome acridine orange. Filtrate studies using P. cepacia 85 suggest that the deforming substance is not a low molecular weight compound. Root hair deformation and the associated wall histology are host specific in that Betula root hairs show none of these responses when grown and inoculated in the experimental conditions described. The bacterially induced changes in root hair cell walls during deformation may create a chemically and physically modified substrate for Frankia penetration, and the deformation itself may serve to entrap and enclose the filamentous organism, allowing wall dissolution and entry. Thus these events represent a complex host response as a precondition to successful nodulation.


1969 ◽  
Vol 22 (2) ◽  
pp. 413 ◽  
Author(s):  
Phaik Y Yao ◽  
JM Vincent

Thirty-eight cultures of rhizobia and 10 non-rhizobia growing in the root zone of clover (Trifolium glomeratum L.), 5 rhizobia and 3 non-rhizobia in that of lucerne (Medicago sativa L.), and 8 rhizobia in that ofSiratro (Phaseolus atropurpureus DO.) revealed a specific relationship between bacteria and host that determined the kind and degree of deformation of the root hairs.


2017 ◽  
Author(s):  
Silvina Mangano ◽  
Silvina Paola Denita-Juarez ◽  
Hee-Seung Choi ◽  
Eliana Marzol ◽  
Youra Hwang ◽  
...  

AbstractRoot hair polar growth is endogenously controlled by auxin and sustained by oscillating levels of reactive oxygen species (ROS). These cells extend several hundred-fold their original size toward signals important for plant survival. Although their final cell size is of fundamental importance, the molecular mechanisms that control it remain largely unknown. Here, we show that ROS production is controlled by the transcription factors RSL4, which in turn is transcriptionally regulated by auxin through several Auxin Responsive Factors (ARFs). In this manner, auxin controls ROS-mediated polar growth by activating RSL4, which then upregulates the expression of genes encoding NADPH oxidases (also known as RBOHs, RESPIRATORY BURST OXIDASE HOMOLOG proteins) and Class-III Peroxidases (PER), which catalyse ROS production. Chemical or genetic interference with the ROS balance or peroxidase activity affect root hair final cell size. Overall, our findings establish a molecular link between auxin regulated ARFs-RSL4 and ROS-mediated polar root hair growth.Significance StatementTip-growing root hairs are excellent model systems to decipher the molecular mechanism underlying reactive oxygen species (ROS)-mediated cell elongation. Root hairs are able to expand in response to external signals, increasing several hundred-fold their original size, which is important for survival of the plant. Although their final cell size is of fundamental importance, the molecular mechanisms that control it remain largely unknown. In this study, we propose a molecular mechanism that links the auxin-Auxin Response Factors (ARFs) module to activation of RSL4, which directly targets genes encoding ROS-producing enzymes, such as NADPH oxidases (or RBOHs) and secreted type-III peroxidases (PERs). Activation of these genes impacts apoplastic ROS homeostasis, thereby stimulating root hair cell elongation.


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