Abstract
The rhizosphere is a hotbed of microbial activity in ecosystems, fueled by carbon compounds from plant roots. Basic questions about the location and dynamics of plant-spurred microbial growth in the rhizosphere are difficult to answer with standard, destructive soil assays mixing a multitude of microbe-scale microenvironments in a single, often sieved, sample. Soil microbial biosensors designed with the luxCDABE reporter genes fused to a promoter of interest enable continuous imaging of the microbial perception of (and response to) environmental conditions in soil. We used the common soil bacterium Pseudomonas putida KT2440 as host to plasmid pZKH2 containing a fusion between the strong constitutive promoter nptII and luxCDABE (coding for light-emitting proteins) from Vibrio fischeri. Experiments in liquid media demonstrated that high light production by KT2440/pZKH2 was associated with rapid microbial growth supported by high carbon availability. We applied the biosensors in microcosms filled with non-sterile soil in which corn (Zea mays L.), black poplar (Populus nigra L.), or tomato (Solanum lycopersicum L.) was growing. We detected minimal light production from microbiosensors in the bulk soil, but biosensors reported continuously from around roots for as long as six days. For corn, peaks of luminescence were detected 1–4 and 20–35 mm along the root axis behind growing root tips, with the location of maximum light production moving farther back from the tip as root growth rate increased. For poplar, luminescence around mature roots increased and decreased on a coordinated diel rhythm, but was not bright near root tips. For tomato, luminescence was dynamic, but did not exhibit a diel rhythm, appearing in acropetal waves along roots. KT2440/pZKH2 revealed that root tips are not always the only, or even the dominant, hotspots for rhizosphere microbial growth, and carbon availability is highly variable in space and time around roots.
Highlights
Most terrestrial plants grow in environments where restricted quantities of water or mineral nutrients limit plant growth
It has long been known that different plant roots release different kinds of carbon compounds, that shoot-root allocation patterns vary widely, and that plant roots grow at different rates depending on environmental conditions
From the perspective of the rhizosphere being a key commodities exchange in ecosystems, this integrated view is essential—many resources may support microbial growth, and a range of conditions exist around plant roots
Summary
Most terrestrial plants grow in environments where restricted quantities of water or mineral nutrients (e.g., nitrogen, phosphorous) limit plant growth. Plants invest a significant amount of fixed carbon into root tissue and rhizodeposition to acquire these limiting resources. As roots grow, they release carbon, in the process stimulating the growth and activities of surrounding microbial community (Wardle, 1992; Cheng et al, 1996). van Veen et al (1991) estimate, for example, that for every 10 grams of carbon assimilated by a plant, an estimated 4 grams are contributed to the soil as rhizodeposition These rhizodeposits provide energy supporting growth and activity of microbes in the rhizosphere (Lynch and Whipps, 1990). Is the energy contribution from roots to microbes a one-time occurrence as the root tip passes by in the soil, or do plants continue to release carbon at the same location again and again? Do known shoot-root carbon allocation patterns in various plant species translate to similar temporal (or spatial) patterns of carbon availability to free-living rhizosphere microbes?
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