Long Distance Transport: Under pressure
Plants use photosynthesis to make sugar in their leaves and other green tissues. They also move excess sugars from these “source” tissues to other parts of the plant, such as the seeds, fruits and roots. In addition to playing crucial roles in the life of the plant, these "sink" tissues are often the edible part of the plant. Indeed, virtually every calorie we consume has travelled from a source tissue to sink tissue at least once, so the system used to transport sugars in plants has a big influence on crop yields.
The long distance transport of sugars occurs in a tissue called phloem. In tall trees, source tissues and sink tissues can be separated by more than 100 meters: it would take over 300,000 years for sugars to diffuse over such a distance, so there must be other mechanisms in place. Now, in eLife, Michael Knoblauch of Washington State University and colleagues tackle long standing questions in the field of phloem transport (Knoblauch et al., 2016).
In flowering plants, cells called sieve elements form the tubes that transport sugars and other molecules through the phloem. These cells adopt a “zombie-like” state as they mature: although they are living cells, they are only able to carry out a limited number of processes compared to other plant cells. The sieve elements are separated by sieve plates, which contain large pores that allow fluid to flow through the phloem. Alongside the phloem, another type of tissue called the xylem transports water and ions away from the roots. Although the phloem and xylem play different roles in the plant, they also depend heavily on each other.
In 1930, the German botanist Ernst Münch proposed that pressure differences between the source and sink tissues are responsible for transport through the phloem (Münch, 1927). In the phloem of source tissues, sugars are highly concentrated, so water is drawn into the sieve tubes from the neighboring xylem. This increases the hydrostatic pressure, which is counteracted by the cell walls of sieve elements, leading to an increase in the turgor pressure. In sink tissues, on the other hand, sugars are consumed, which reduces their concentration in the phloem: this allows water to flow back into the xylem and leads to a decrease in the turgor pressure.
Münch proposed that the difference in turgor pressure between the source and the sink is sufficient to drive long-distance transport without the need of additional energy. This so-called “pressure flow hypothesis” is very intuitive and has been taught at universities for decades despite there being only limited experimental evidence to support it. It is technically challenging to perform experiments on phloem because the tissue is often deeply embedded in the plant and it is difficult to isolate sieve tubes.
The Knoblauch lab has a long history of developing techniques to measure the biophysical characteristics of flow through the phloem and xylem (Knoblauch and van Bel, 1998; Mullendore et al., 2010; Froelich et al., 2011; Jensen et al., 2012; Knoblauch et al., 2014). Now, they have used these methods to calculate the flow of fluid through the phloem of a type of vine called Morning Glory (Ipomea nil), which can grow up to 15 meters in length.
If the Münch hypothesis is right, there should be differences in turgor pressure and phloem conductivity (the ability of fluid to move through the phloem) between tall and short plants. Knoblauch and colleagues – who are based at Washington State University, Harvard University, the Brookhaven National Laboratory and the Technical University of Denmark – allowed individual morning glory plants to grow to several different lengths (Figure 1). The plants had their lower leaves removed so that the only leaves remaining were on the top four meters of each plant. The experiments demonstrate that taller plants have larger differences in turgor pressure between source and sink compared to shorter plants. Furthermore, phloem tubes have higher conductivities in taller plants than in shorter plants because the pores in their sieve plates are larger.
This study provides a long-awaited experimental proof of Münch’s pressure flow hypothesis. One of the most striking findings is the observation that, in contrast to a generally accepted theory, the unloading of sugars from phloem in sink tissues is very likely to involve additional inputs of energy. This implies that transporter proteins that unload nutrients from the phloem – like the SWEET and UmamiT proteins – play much more important roles than previously thought (Chen et al., 2012; 2015; Muller et al., 2015). Their biophysical properties need to be investigated in much greater detail to understand their role in phloem transport. Another question for future research is how plants control the distribution of resources between tissues for storage or growth. Last but not least, the precise molecular mechanisms of phloem loading, particularly in trees, are still a matter of debate that needs to be investigated.
References
-
Modeling the hydrodynamics of phloem sieve platesFrontiers in Plant Science 3:151.https://doi.org/10.3389/fpls.2012.00151
-
Pico gauges for minimally invasive intracellular hydrostatic pressure measurementsPlant Physiology 166:1271–1279.https://doi.org/10.1104/pp.114.245746
-
Sieve tube geometry in relation to phloem flowPlant Cell 22:579–593.https://doi.org/10.1105/tpc.109.070094
-
Versuche über den SaftkreislaufBerichte der Deutschen Botanischen Gesellschaft 45:340–356.https://doi.org/10.1111/j.1438-8677.1927.tb01184.x
Article and author information
Author details
Publication history
Copyright
© 2016, Hammes
This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.
Metrics
-
- 2,375
- views
-
- 204
- downloads
-
- 0
- citations
Views, downloads and citations are aggregated across all versions of this paper published by eLife.
Download links
Downloads (link to download the article as PDF)
Open citations (links to open the citations from this article in various online reference manager services)
Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)
Further reading
-
- Plant Biology
Obligate parasites often trigger significant changes in their hosts to facilitate transmission to new hosts. The molecular mechanisms behind these extended phenotypes - where genetic information of one organism is manifested as traits in another - remain largely unclear. This study explores the role of the virulence protein SAP54, produced by parasitic phytoplasmas, in attracting leafhopper vectors. SAP54 is responsible for the induction of leaf-like flowers in phytoplasma-infected plants. However, we previously demonstrated that the insects were attracted to leaves and the leaf-like flowers were not required. Here, we made the surprising discovery that leaf exposure to leafhopper males is required for the attraction phenotype, suggesting a leaf response that distinguishes leafhopper sex in the presence of SAP54. In contrast, this phytoplasma effector alongside leafhopper females discourages further female colonization. We demonstrate that SAP54 effectively suppresses biotic stress response pathways in leaves exposed to the males. Critically, the host plant MADS-box transcription factor short vegetative phase (SVP) emerges as a key element in the female leafhopper preference for plants exposed to males, with SAP54 promoting the degradation of SVP. This preference extends to female colonization of male-exposed svp null mutant plants over those not exposed to males. Our research underscores the dual role of the phytoplasma effector SAP54 in host development alteration and vector attraction - integral to the phytoplasma life cycle. Importantly, we clarify how SAP54, by targeting SVP, heightens leaf vulnerability to leafhopper males, thus facilitating female attraction and subsequent plant colonization by the insects. SAP54 essentially acts as a molecular ‘matchmaker’, helping male leafhoppers more easily locate mates by degrading SVP-containing complexes in leaves. This study not only provides insights into the long reach of single parasite genes in extended phenotypes, but also opens avenues for understanding how transcription factors that regulate plant developmental processes intersect with and influence plant-insect interactions.
-
- Microbiology and Infectious Disease
- Plant Biology
Programmed cell death occurring during plant development (dPCD) is a fundamental process integral for plant growth and reproduction. Here, we investigate the connection between developmentally controlled PCD and fungal accommodation in Arabidopsis thaliana roots, focusing on the root cap-specific transcription factor ANAC033/SOMBRERO (SMB) and the senescence-associated nuclease BFN1. Mutations of both dPCD regulators increase colonization by the beneficial fungus Serendipita indica, primarily in the differentiation zone. smb-3 mutants additionally exhibit hypercolonization around the meristematic zone and a delay of S. indica-induced root-growth promotion. This demonstrates that root cap dPCD and rapid post-mortem clearance of cellular corpses represent a physical defense mechanism restricting microbial invasion of the root. Additionally, reporter lines and transcriptional analysis revealed that BFN1 expression is downregulated during S. indica colonization in mature root epidermal cells, suggesting a transcriptional control mechanism that facilitates the accommodation of beneficial microbes in the roots.