scholarly journals Biological nitrification inhibition in maize—isolation and identification of hydrophobic inhibitors from root exudates

Author(s):  
Junnosuke Otaka ◽  
Guntur Venkata Subbarao ◽  
Hiroshi Ono ◽  
Tadashi Yoshihashi

AbstractTo control agronomic N losses and reduce environmental pollution, biological nitrification inhibition (BNI) is a promising strategy. BNI is an ecological phenomenon by which certain plants release bioactive compounds that can suppress nitrifying soil microbes. Herein, we report on two hydrophobic BNI compounds released from maize root exudation (1 and 2), together with two BNI compounds inside maize roots (3 and 4). On the basis of a bioassay-guided fractionation method using a recombinant nitrifying bacterium Nitrosomonas europaea, 2,7-dimethoxy-1,4-naphthoquinone (1, ED50 = 2 μM) was identified for the first time from dichloromethane (DCM) wash concentrate of maize root surface and named “zeanone.” The benzoxazinoid 2-hydroxy-4,7-dimethoxy-2H-1,4-benzoxazin-3(4H)-one (HDMBOA, 2, ED50 = 13 μM) was isolated from DCM extract of maize roots, and two analogs of compound 2, 2-hydroxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one (HMBOA, 3, ED50 = 91 μM) and HDMBOA-β-glucoside (4, ED50 = 94 μM), were isolated from methanol extract of maize roots. Their chemical structures (1–4) were determined by extensive spectroscopic methods. The contributions of these four isolated BNI compounds (1–4) to the hydrophobic BNI activity in maize roots were 19%, 20%, 2%, and 4%, respectively. A possible biosynthetic pathway for zeanone (1) is proposed. These results provide insights into the strength of hydrophobic BNI activity released from maize root systems, the chemical identities of the isolated BNIs, and their relative contribution to the BNI activity from maize root systems.

Author(s):  
Arindam Ghatak ◽  
Florian Schindler ◽  
Gert Bachmann ◽  
Doris Engelmeier ◽  
Prasad Bajaj ◽  
...  

AbstractRoots secrete a vast array of low molecular weight compounds into the soil broadly referred to as root exudates. It is a key mechanism by which plants and soil microbes interact in the rhizosphere. The effect of drought stress on the exudation process and composition is rarely studied, especially in cereal crops. This study focuses on comparative metabolic profiling of the exudates from sensitive and tolerant genotypes of pearl millet after a period of drought stress. We employed a combined platform of gas and liquid chromatography coupled to mass spectrometry to cover both primary and secondary metabolites. The results obtained demonstrate that both genotype and drought stress have a significant impact on the concentration and composition of root exudates. The complexity and function of these differential root exudates are discussed. To reveal the potential effect of root exudates on the soil microbial community after a period of drought stress, we also tested for biological nitrification inhibition (BNI) activity. The analysis revealed a genotype-dependent enhancement of BNI activity after a defined period of drought stress. In parallel, we observed a genotype-specific relation of elongated root growth and root exudation under drought stress. These data suggest that the drought stress-dependent change in root exudation can manipulate the microbial soil communities to adapt and survive under harsh conditions.


2021 ◽  
Author(s):  
Pauline Sophie Rummel ◽  
Reinhard Well ◽  
Birgit Pfeiffer ◽  
Klaus Dittert ◽  
Sebastian Floßmann ◽  
...  

<p>The main prerequisites for denitrification are availability of nitrate (NO<sub>3</sub><sup>-</sup>) and easily decomposable organic substances, and oxygen deficiency. Growing plants modify all these parameters and may thus play an important role in regulating denitrification. Previous studies investigating plant root effects on denitrification have found contradictive results. Both increased and decreased denitrification in the presence of plants have been reported and were associated with higher C<sub>org</sub> or lower NO<sub>3</sub><sup>-</sup> availability, respectively. Accordingly, it is still unclear whether growing plants stimulate denitrification through root exudation or restrict it through NO<sub>3</sub><sup>-</sup> uptake. Furthermore, reliable measurements of N<sub>2</sub> fluxes and N<sub>2</sub>O/(N<sub>2</sub>O+N<sub>2</sub>) ratios in the presence of plants are scarce.</p><p>Therefore, we conducted a double labeling pot experiment with either maize (<em>Zea mays</em> L.) or cup plant (<em>Silphium perfoliatum</em> L.) of the same age but differing in size of their shoot and root systems. The <sup>15</sup>N gas flux method was applied to directly quantify N<sub>2</sub>O and N<sub>2</sub> fluxes in situ. To link denitrification with available C in the rhizosphere, <sup>13</sup>CO<sub>2</sub> pulse labeling was used to trace C translocation from shoots to roots and its release by roots into the soil.</p><p>Plant water uptake was a main factor controlling soil moisture and, thus, daily N<sub>2</sub>O+N<sub>2</sub> fluxes, cumulative N emissions, and N<sub>2</sub>O production pathways. However, N fluxes remained on a low level when NO<sub>3</sub><sup>-</sup> availability was low due to rapid plant N uptake. Only when both N and water uptake were low, high NO<sub>3</sub><sup>-</sup> availability and high soil moisture led to strongly increased denitrification-derived N losses.</p><p>Total CO<sub>2</sub> efflux was positively correlated with root dry matter, but there was no indication of any relationship between recovered <sup>13</sup>C from root exudation and cumulative N emissions. We anticipate that higher C<sub>org</sub> availability in pots with large root systems did not lead to higher denitrification rates, as NO<sub>3</sub><sup>-</sup> was limiting denitrification due to plant N uptake. Overall, we conclude that root-derived C stimulates denitrification only when soil NO<sub>3</sub><sup>-</sup> is not limited and low O<sub>2</sub> concentrations enable denitrification. Thus, root-derived C may stimulate denitrification under small plants, while N and water uptake become the controlling factors with increasing plant and root growth.</p>


2020 ◽  
Vol 44 (6) ◽  
pp. 874-908
Author(s):  
Pierfrancesco Nardi ◽  
Hendrikus J Laanbroek ◽  
Graeme W Nicol ◽  
Giancarlo Renella ◽  
Massimiliano Cardinale ◽  
...  

ABSTRACT Nitrification is the microbial conversion of reduced forms of nitrogen (N) to nitrate (NO3−), and in fertilized soils it can lead to substantial N losses via NO3− leaching or nitrous oxide (N2O) production. To limit such problems, synthetic nitrification inhibitors have been applied but their performance differs between soils. In recent years, there has been an increasing interest in the occurrence of biological nitrification inhibition (BNI), a natural phenomenon according to which certain plants can inhibit nitrification through the release of active compounds in root exudates. Here, we synthesize the current state of research but also unravel knowledge gaps in the field. The nitrification process is discussed considering recent discoveries in genomics, biochemistry and ecology of nitrifiers. Secondly, we focus on the ‘where’ and ‘how’ of BNI. The N transformations and their interconnections as they occur in, and are affected by, the rhizosphere, are also discussed. The NH4+ and NO3− retention pathways alternative to BNI are reviewed as well. We also provide hypotheses on how plant compounds with putative BNI ability can reach their targets inside the cell and inhibit ammonia oxidation. Finally, we discuss a set of techniques that can be successfully applied to solve unresearched questions in BNI studies.


2009 ◽  
Vol 59 (5) ◽  
pp. 529-545 ◽  
Author(s):  
Guntur Venkata Subbarao ◽  
Masahiro Kishii ◽  
Kazuhiko Nakahara ◽  
Takayuki Ishikawa ◽  
Tomohiro Ban ◽  
...  

2018 ◽  
Vol 426 (1-2) ◽  
pp. 401-411 ◽  
Author(s):  
Jonathan Nuñez ◽  
Ashly Arevalo ◽  
Hannes Karwat ◽  
Konrad Egenolf ◽  
John Miles ◽  
...  

2019 ◽  
Vol 2 (1) ◽  
Author(s):  
Félicien Meunier ◽  
Adrien Heymans ◽  
Xavier Draye ◽  
Valentin Couvreur ◽  
Mathieu Javaux ◽  
...  

Abstract Functional-structural root system models combine functional and structural root traits to represent the growth and development of root systems. In general, they are characterized by a large number of growth, architectural and functional root parameters, generating contrasted root systems evolving in a highly non-linear environment (soil, atmosphere), which makes the link between local traits and functioning unclear. On the other end of the root system modelling continuum, macroscopic root system models associate to each root system a set of plant-scale, easily interpretable parameters. However, as of today, it is unclear how these macroscopic parameters relate to root-scale traits and whether the upscaling of local root traits is compatible with macroscopic parameter measurements. The aim of this study was to bridge the gap between these two modelling approaches. We describe here the MAize Root System Hydraulic Architecture soLver (MARSHAL), a new efficient and user-friendly computational tool that couples a root architecture model (CRootBox) with fast and accurate algorithms of water flow through hydraulic architectures and plant-scale parameter calculations. To illustrate the tool’s potential, we generated contrasted maize hydraulic architectures that we compared with root system architectural and hydraulic observations. Observed variability of these traits was well captured by model ensemble runs. We also analysed the multivariate sensitivity of mature root system conductance, mean depth of uptake, root system volume and convex hull to the input parameters to highlight the key model parameters to vary for virtual breeding. It is available as an R package, an RMarkdown pipeline and a web application.


2018 ◽  
Vol 28 (5) ◽  
pp. 629-636 ◽  
Author(s):  
Matthew B. Bertucci ◽  
David H. Suchoff ◽  
Katherine M. Jennings ◽  
David W. Monks ◽  
Christopher C. Gunter ◽  
...  

Grafting of watermelon (Citrullus lanatus) is an established production practice that provides resistance to soilborne diseases or tolerance to abiotic stresses. Watermelon may be grafted on several cucurbit species (interspecific grafting); however, little research exists to describe root systems of these diverse rootstocks. A greenhouse study was conducted to compare root system morphology of nine commercially available cucurbit rootstocks, representing four species: pumpkin (Cucurbita maxima), squash (Cucurbita pepo), bottle gourd (Lagenaria siceraria), and an interspecific hybrid squash (C. maxima × C. moschata). Rootstocks were grafted with a triploid watermelon scion (‘Exclamation’), and root systems were compared with nongrafted (NG) and self-grafted (SG) ‘Exclamation’. Plants were harvested destructively at 1, 2, and 3 weeks after transplant (WAT), and data were collected on scion dry weight, total root length (TRL), average root diameter, root surface area, root:shoot dry-weight ratio, root diameter class proportions, and specific root length. For all response variables, the main effect of rootstock and rootstock species was significant (P < 0.05). The main effect of harvest was significant (P < 0.05) for all response variables, with the exception of TRL proportion in diameter class 2. ‘Ferro’ rootstock produced the largest TRL and root surface area, with observed values 122% and 120% greater than the smallest root system (‘Exclamation’ SG), respectively. Among rootstock species, pumpkin produced the largest TRL and root surface area, with observed values 100% and 82% greater than those of watermelon, respectively. These results demonstrate that substantial differences exist during the initial 3 WAT in root system morphology of rootstocks and rootstock species available for watermelon grafting and that morphologic differences of root systems can be characterized using image analysis.


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