Attachment to Plant Root Surface and Nitrogenase Activity of Rhizobia Associated with Petunia Plants

1980 ◽  
Vol 98 (5) ◽  
pp. 465-470 ◽  
Author(s):  
E.-M. Götz
2020 ◽  
Author(s):  
Pallavi Kumari ◽  
Tali Sayas ◽  
Patricia Bucki ◽  
Sigal Brown Miyara ◽  
Maya Kleiman

AbstractStudying the interactions between microorganisms and plant roots is crucial for understanding a variety of phenomena concerning crop yield and health. The role of root surface properties in these interactions, is rarely addressed. To this end, we previously built a synthetic system, from the inert polymer polydimethyl siloxane (PDMS), mimicking the root surface microstructure, using a replication technique. This replica enables the study of isolated effects of surface structure on microorganism-plant interactions. Since the root surface is composed mostly of cellulose, using cellulose-like materials as our replica, instead of PDMS, is the next logical step. This will enable following the hydrolysis of such surfaces as a result of microorganisms secreting Plant Cell Wall Degrading Enzymes (PCWDE), and in particular, cellulase. Visualization of such hydrolysis in a synthetic system can assist in studying the localization and activity of microorganisms and how they correlate with surface microtopography, separately from chemical plant signals.In this work, we modified the known carboxymethyl cellulase (CMC) hydrolysis visualization method to enable real-time tracking of cellulase activity of microorganisms on the surface. Surface was formed from pure CMC, rather than CMC incorporated in agar as is often done, and by that, eliminating diffusion issues. Acridine orange dye, which is compatible, at low concentrations, with microorganisms, as opposed to other routinely used dyes, was incorporated into the film. The dye disassociated from the film when hydrolysis occurred, forming a halo surrounding the point of hydrolysis. This enabled real-time visualization since the common need for post hydrolysis dyeing was negated. Using Root Knot Nematode (RKN) as a model organism that penetrates the plant root, we showed it was possible to follow microorganism cellulase secretion on the surface in the form of CMC film hydrolysis. Furthermore, the addition of natural additives, in the form of root extract was also shown to be an option and resulted in an increased RKN response. We tested our newly developed method by changing temperature and pH conditions and by characterization of the hydrolyzed surface using both Scanning Electron Microscopy (SEM) and Atomic Force Microscopy (AFM).This method will be implemented in the future on a root surface microstructure replica. We believe the combination of this new method with our previously developed root surface microstructure replication technique can open a new avenue of research in the field of plant root-microorganism interactions.


Author(s):  
Peter B. Tinker ◽  
Peter Nye

We discussed in chapter 4 the movement of solute between small volumes of soil, and in chapter 5 some properties of plant roots and associated hairs, particularly the relation between the rate of uptake at the root surface and the concentration of solute in the ambient solution. In the chapters to follow, we consider the plant root in contact with the soil, and deal with their association in increasingly complex situations; first, when the root acts merely as a sink and, second, when it modifies its relations with the surrounding soil by changing its pH, excreting ions, stimulating microorganisms, or developing mycorrhizas. In this chapter, we take the simplest situation that can be studied in detail, namely, a single intact root alone in a volume of soil so large that it can be considered infinite. The essential transport processes occurring near the root surface are illustrated in figure 6.1. We have examined in chapter 3 the rapid dynamic equilibrium between solutes in the soil pore solution and those sorbed on the immediately adjacent solid surfaces. These sorbed solutes tend to buffer the soil solution against changes in concentration induced by root uptake. At the root surface, solutes are absorbed at a rate related to their concentration in the soil solution at the boundary (section 5.3.2); and the root demand coefficient, αa, is defined by the equation . . . I = 2παaCLa (6.1) . . . where I = inflow (rate of uptake per unit length), a = root radius, CLa = concentration in solution at the root surface. To calculate the inflow, we have to know CLa, and the main topic of this chapter is the relation between CLa, and the soil pore solution concentration CL. The root also absorbs water at its surface due to transpiration (chapter 2) so that the soil solution flows through the soil pores, thus carrying solutes to the root surface by mass flow (convection). Barber et al. (1962) calculated whether the nutrients in maize could be acquired solely by this process, by multiplying the composition of the soil solution by the amount of water the maize had transpired.


1982 ◽  
Vol 60 (6) ◽  
pp. 888-896 ◽  
Author(s):  
F. D. H. Macdowall

Measurements were made of plant, root, and nodule dry matter, nodule number, acetylene reduction by nitrogenase, plant N content, and shoot height of Medicago sativa L. cv. Algonquin and expressed chiefly as rate constants of growth (k1′). The effects of the nature and quantity of solid substratum, of the form and concentration of combined N and of symbiotic and non-symbiotic growth, were compared in optimum growth room conditions. Plants grew at the same maximum k1′ in vermiculite with or without gravel and in a soil mix when supplied with 15 mM NO3− in the nutrient solution. Plant growth was retarded with decreasing pot size but maximum nodule growth k1′ occurred in 7-cm pots. Nodulation and nitrogenase activity showed maximum k1′ with least added N but moderate additions produced larger yields of roots and nodules. Plant growth in dry matter and N content, expressed as k1′, yield, or absolute rate (k1′∙yield), was under no circumstance increased by symbiosis in this phase of exponential growth. Nodulation was completely inhibited by 15 mM NO3− and higher concentrations of N were generally inhibitory. A transient, postgerminative treatment with 15 mM NO3− provided a sustained boost to growth. Combined N supplied as NO2− or NH4+ at 15 mM in the nutrient solution without NO3− suported k1′ values comparable to those obtained with less than 1.5 mM NO3−.


2015 ◽  
Vol 81 (21) ◽  
pp. 7484-7495 ◽  
Author(s):  
Pauline Woan Ying Liew ◽  
Bor Chyan Jong ◽  
Nazalan Najimudin

ABSTRACTA proteomic analysis of a soil-dwelling, plant growth-promotingAzotobacter vinelandiistrain showed the presence of a protein encoded by the hypotheticalAvin_16040gene when the bacterial cells were attached to theOryza sativaroot surface. AnAvin_16040deletion mutant demonstrated reduced cellular adherence to the root surface, surface hydrophobicity, and biofilm formation compared to those of the wild type. By atomic force microscopy (AFM) analysis of the cell surface topography, the deletion mutant displayed a cell surface architectural pattern that was different from that of the wild type.Escherichia colitransformed with the wild-typeAvin_16040gene displayed on its cell surface organized motifs which looked like the S-layer monomers ofA. vinelandii. The recombinantE. colialso demonstrated enhanced adhesion to the root surface.


1984 ◽  
Vol 62 (9) ◽  
pp. 1965-1967 ◽  
Author(s):  
David D. Biesboer

Seasonal changes in nitrogen fixation, numbers of nitrogen-fixing bacteria associated with the roots, and rhizome–root carbohydrates were studied for the broad-leaved cattail, Typha latifolia L. Populations of anaerobic and aerobic diazotrophic bacteria were present on the root surface. Anaerobic bacteria predominated in the diazotrophic association, were more active in the acetylene reduction assay, and generally outnumbered aerobic bacteria by 2 to 1 during maximum rates of seasonal nitrogen fixation. The observed maximum nitrogen fixation rate coincided closely with reproductive development in Typha and peak microbial populations. Starch levels in rhizomes were nearly depleted during the middle of the growing season, whereas free sugar concentrations remained stable. Sugar concentrations in the roots increased rapidly during rhizome–root growth and decreased rapidly prior to peak nitrogenase activity.


2021 ◽  
Vol 49 (2) ◽  
pp. 12258
Author(s):  
Xian HUANG ◽  
Tianzhi GONG ◽  
Mei LI ◽  
Cenghong HU ◽  
Dejian ZHANG ◽  
...  

Plant root hairs are cylindrical tubular projections from root epidermal cells. They increase the root surface area, which is important for the acquisition of water and nutrients, microbe interactions, and plant anchorage. The root hair specification, the effect of root hairs on nutrient acquisition and the mechanisms of nutrients (calcium, iron, magnesium, nitrogen, phosphorus, and potassium) that affect root hair development and growth were reviewed. The gene regulatory network on root hair specification in the plant kingdom was highlighted. More work is needed to clone the genes of additional root hair mutants and elucidate their roles, as well as undertaking reverse genetics and mutant complementation studies to add to the current knowledge of the signaling networks, which are involved in root hair development and growth regulated by nutrients.


Author(s):  
Shinichi Ogiyama ◽  
Nobuyoshi Ishii ◽  
Shigeo Uchida

Experiments using rice plants (Oryza sativa L.) were conducted to examine uptake of 14C-acetic acid via the root and 14C behavior on the root surface. For hydroponics, three types of rice plants were cultured with 14C-acetic acid solution: complete plant, half-rooted plant, and non-rooted plant. Also, for the root incubation experiment, sterilized root and non-sterilized root were incubated with 14C-acetic acid solution. The 14C radioactivities in the plant parts and solution were measured. Non- and half-rooted plant had 14C radioactivity in their aerial part, but the complete plant did not. The trends of radioactivity levels in the solution were directly opposite to those of plant root biomass. A high level of 14C radioactivity was observed on the entire root surface of non-sterilized root in the incubation experiment, and 14C radioactivity in the solution also remarkably decreased from 7 h to 96 h after the 14C addition. These results suggest that the amount of 14C-acetic acid absorbed by the plant through the roots is very small. However, the plant absorbs 14C-acetic acid through breaks in the roots. Once 14C-acetic acid is inside the plant, it immediately transfers to the shoots. Degradation of 14C radioactivity in the solution and 14C fixation on the root surface arise from the context of microbial activities.


1993 ◽  
Vol 39 (4) ◽  
pp. 420-429 ◽  
Author(s):  
J. Katsuwon ◽  
R. Zdor ◽  
A. J. Anderson

Several saprophytic fluorescent pseudomonads that are aggressive root colonizers express similar specific activities of superoxide dismutase during growth in liquid culture. The pseudomonads have the potential to produce hydrogen peroxide sensitive and hydrogen peroxide insensitive isoforms of superoxide dismutase with distinct mobilities in nondenaturing polyacrylamide gel electrophoresis. Synthesis of the hydrogen peroxide insensitive form is enhanced by limited iron availability, by exposure to Mn2+, and to a lesser extent by external sources of superoxide anion. Unlike Pseudomonas aeruginosa, a root-colonizing strain of Pseudomonas putida did not show regulation of isoform pattern by phosphate availability. A plasmid potentially encoding the pseudomonad hydrogen peroxide sensitive form complemented the superoxide dismutase deficiency in a mutant of Escherichia coli lacking expression of both Fe and Mn genes. Contact between the plant root and pseudomonad or E. coli cells that lack or express superoxide dismutase did not influence superoxide anion production from root surface enzymes. The pseudomonad and the superoxide dismutase deficient and producing E. coli strains survived exposure to the root equally well. Only the hydrogen peroxide sensitive isoform of superoxide dismutase was detected in P. putida cells associated with bean root surfaces.Key words: pseudomonads, activated oxygen, root surface colonization.


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