Rhizobia

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Root nodules, each containing billions of Rhizobiaceae bacteria Soybean-root-nodules.jpg
Root nodules, each containing billions of Rhizobiaceae bacteria

Rhizobia are diazotrophic bacteria that fix nitrogen after becoming established inside the root nodules of legumes (Fabaceae). To express genes for nitrogen fixation, rhizobia require a plant host; they cannot independently fix nitrogen. [1] In general, they are gram negative, motile, non-sporulating rods.

Contents

Rhizobia are a "group of soil bacteria that infect the roots of legumes to form root nodules". [2] Rhizobia are found in the soil and, after infection, produce nodules in the legume where they fix nitrogen gas (N2) from the atmosphere, turning it into a more readily useful form of nitrogen. From here, the nitrogen is exported from the nodules and used for growth in the legume. Once the legume dies, the nodule breaks down and releases the rhizobia back into the soil, where they can live individually or reinfect a new legume host. [2]

History

The first known species of rhizobia, Rhizobium leguminosarum , was identified in 1889, and all further species were initially placed in the Rhizobium genus. Most research has been done on crop and forage legumes such as clover, alfalfa, beans, peas, and soybeans; more research is being done on North American legumes.[ citation needed ]

Taxonomy [lower-alpha 1]

Rhizobia are a paraphyletic group that fall into two classes of Pseudomonadota the alphaproteobacteria and betaproteobacteria. As shown below, most belong to the order Hyphomicrobiales, but several rhizobia occur in distinct bacterial orders of the Pseudomonadota. [3] [4] [5] [6]

Alphaproteobacteria

Hyphomicrobiales (syn. Rhizobiales)
Nitrobacteraceae
Bosea
Bradyrhizobium
B. arachidis
B. canariense
B. cytisi
B. daqingense
B. denitrificans
B. diazoefficiens
B. elkanii
B. huanghuaihaiense
B. iriomotense
B. japonicum
B. jicamae
B. lablabi
B. liaoningense
B. pachyrhizi
B. rifense
B. yuanmingense
Brucellaceae
Ochrobactrum
O. cytisi
O. lupini
Hyphomicrobiaceae
Devosia
D. neptuniae
Methylobacteriaceae
Methylobacterium
M. nodulans
Microvirga
M. lotononidis
M. lupini
M. zambiensis
Phyllobacteriaceae
Aminobacter
A. anthyllidis
Mesorhizobium
M. abyssinicae
M. albiziae
M. alhagi
M. amorphae
M. australicum
M. camelthorni
M. caraganae
M. chacoense
M. ciceri
M. gobiense
M. hawassense
M. huakuii
M. loti
M. mediterraneum
M. metallidurans
M. muleiense
M. opportunistum
M. plurifarium
M. qingshengii
M. robiniae
M. sangaii
M. septentrionale
M. shangrilense
M. shonense
M. tamadayense
M. tarimense
M. temperatum
M. tianshanense
Phyllobacterium
P. sophorae
P. trifolii
Rhizobiaceae
Rhizobium
R. alamii
R. cauense
R. cellulosilyticum
R. daejeonense
R. etli
R. fabae
R. gallicum
R. grahamii
R. hainanense
R. halophytocola
R. indigoferae
R. leguminosarum
R. leucaenae
R. loessense
R. lupini
R. lusitanum
R. mesoamericanum
R. mesosinicum
R. miluonense
R. mongolense
R. multihospitium
R. oryzae
R. petrolearium
R. phaseoli
R. pisi
R. qilianshanense
R. sullae
R. taibaishanense
R. tibeticum
R. tropici
R. tubonense
R. vallis
R. yanglingense
Agrobacterium
A. nepotum
A. pusense
Allorhizobium
A. undicola


Pararhizobium
P. giardinii
P. helanshanense
P. herbae
P. sphaerophysae
Neorhizobium
N. alkalisoli
N. galegae
N. huautlense
N. vignae
Shinella
S. kummerowiae
Ensifer (syn. Sinorhizobium )
E. abri
E. adhaerens
E. americanus
E. arboris
E. chiapanecum
E. fredii
E. garamanticus
E. indiaense
E. kostiense
E. kummerowiae
E. medicae
E. meliloti
E. mexicanus
E. numidicus
E. psoraleae
E. saheli
E. sesbaniae
E. sojae
E. terangae
Xanthobacteraceae
Azorhizobium
A. caulinodans
A. doebereinerae

Betaproteobacteria

Burkholderiales
Burkholderiaceae
Cupriavidus
C. taiwanensis
Paraburkholderia
P. caribensis
P. diazotrophica
P. dilworthii
P. mimosarum
P. nodosa
P. phymatum
P. piptadeniae
P. rhynchosiae
P. sabiae
P. sprentiae
P. symbiotica
P. tuberum

These groups include a variety of non-symbiotic bacteria. For instance, the plant pathogen Agrobacterium is a closer relative of Rhizobium than the Bradyrhizobium that nodulate soybean. [7]

Importance in agriculture

Rhizobia nodules on Vigna unguiculata Rhizobia nodules on Vigna unguiculata.jpg
Rhizobia nodules on Vigna unguiculata

Although much of the nitrogen is removed when protein-rich grain or hay is harvested, significant amounts can remain in the soil for future crops. This is especially important when nitrogen fertilizer is not used, as in organic rotation schemes or in some less-industrialized countries. [8] Nitrogen is the most commonly deficient nutrient in many soils around the world and it is the most commonly supplied plant nutrient. The supply of nitrogen through fertilizers has severe environmental concerns.

Specific strains of rhizobia are required to make functional nodules on the roots able to fix the N2. [9] Having this specific rhizobia present is beneficial to the legume, as the N2 fixation can increase crop yield. [10] Inoculation with rhizobia tends to increase yield. [11]

Legume inoculation has been an agricultural practice for many years and has continuously improved over time. [10] 12–20 million hectares of soybeans are inoculated annually. An ideal inoculant includes some of the following aspects; maximum efficacy, ease of use, compatibility, high rhizobial concentration, long shelf-life, usefulness under varying field conditions, and survivability. [10] [12] [13]

These inoculants may foster success in legume cultivation. [14] As a result of the nodulation process, after the harvest of the crop, there are higher levels of soil nitrate, which can then be used by the next crop.

Symbiotic relationship

Rhizobia are unique in that they are the only nitrogen-fixing bacteria living in a symbiotic relationship with legumes. Common crop and forage legumes are peas, beans, clover, and soy.

Nature of the mutualism

The legume–rhizobium symbiosis is a classic example of mutualism rhizobia supply ammonia or amino acids to the plant and, in return, receive organic acids (mainly malate and succinate, which are dicarboxylic acids) as a carbon and energy source. However, because several unrelated strains infect each individual plant, a classic tragedy of the commons scenario presents itself. Cheater strains may hoard plant resources such as polyhydroxybutyrate for the benefit of their own reproduction without fixing an appreciable amount of nitrogen. [15] Given the costs involved in nodulation and the opportunity for rhizobia to cheat, it may be surprising that this symbiosis exists.

Infection and signal exchange

The formation of the symbiotic relationship involves a signal exchange between both partners that leads to mutual recognition and the development of symbiotic structures. The most well understood mechanism for the establishment of this symbiosis is through intracellular infection. Rhizobia are free living in the soil until they are able to sense flavonoids, derivatives of 2-phenyl-1.4-benzopyrone, which are secreted by the roots of their host plant, triggering the accumulation of a large population of cells and eventually attachment to root hairs. [16] [17] These flavonoids then promote the DNA binding activity of NodD, which belongs to the LysR family of transcriptional regulators and triggers the secretion of nod factors after the bacteria have entered the root hair. [17] Nod factors trigger a series of complex developmental changes inside the root hair, beginning with root hair curling and followed by the formation of the infection thread, a cellulose lined tube that the bacteria use to travel down through the root hair into the root cells. [18] The bacteria then infect several other adjacent root cells. This is followed by continuous cell proliferation, resulting in the formation of the root nodule. [16] A second mechanism, used especially by rhizobia that infect aquatic hosts, is called crack entry. In this case, no root hair deformation is observed. Instead, the bacteria penetrate between cells through cracks produced by lateral root emergence. [19]

Inside the nodule, the bacteria differentiate morphologically into bacteroids and fix atmospheric nitrogen into ammonium using the enzyme nitrogenase. Ammonium is then converted into amino acids like glutamine and asparagine before it is exported to the plant. [16] In return, the plant supplies the bacteria with carbohydrates in the form of organic acids. [16] The plant also provides the bacteroid oxygen for cellular respiration, tightly bound by leghaemoglobins, plant proteins similar to human hemoglobins. This process keeps the nodule oxygen poor in order to prevent the inhibition of nitrogenase activity. [16]

Recently, a Bradyrhizobium strain was discovered to form nodules in Aeschynomene without producing nod factors, suggesting the existence of alternative communication signals other than nod factors, possibly involving the secretion of the plant hormone cytokinin. [16] [20]

It has been observed that root nodules can be formed spontaneously in Medicago without the presence of rhizobia. [21] This implies that the development of the nodule is controlled entirely by the plant and simply triggered by the secretion of nod factors.

Evolutionary hypotheses

The sanctions hypothesis

There are two main hypotheses for the mechanism that maintains legume-rhizobium symbiosis (though both may occur in nature). The sanctions hypothesis theorizes that legumes cannot recognize the more parasitic or less nitrogen fixing rhizobia and must counter the parasitism by post-infection legume sanctions. In response to underperforming rhizobia, legume hosts can respond by imposing sanctions of varying severity to their nodules. [22] These sanctions include, but are not limited to, reduction of nodule growth, early nodule death, decreased carbon supply to nodules, or reduced oxygen supply to nodules that fix less nitrogen. Within a nodule, some of the bacteria differentiate into nitrogen fixing bacteroids, which have been found to be unable to reproduce. [23] Therefore, with the development of a symbiotic relationship, if the host sanctions hypothesis is correct, the host sanctions must act toward whole nodules rather than individual bacteria because individual targeting sanctions would prevent any reproducing rhizobia from proliferating over time. This ability to reinforce a mutual relationship with host sanctions pushes the relationship toward mutualism rather than parasitism and is likely a contributing factor to why the symbiosis exists.

However, other studies have found no evidence of plant sanctions. [24]

The partner choice hypothesis

The partner choice hypothesis proposes that the plant uses prenodulation signals from the rhizobia to decide whether to allow nodulation, and chooses only noncheating rhizobia. There is evidence for sanctions in soybean plants, which reduce rhizobium reproduction (perhaps by limiting oxygen supply) in nodules that fix less nitrogen. [25] Likewise, wild lupine plants allocate fewer resources to nodules containing less-beneficial rhizobia, limiting rhizobial reproduction inside. [26] This is consistent with the definition of sanctions, although called "partner choice" by the authors. Some studies support the partner choice hypothesis. [27] While both mechanisms no doubt contribute significantly to maintaining rhizobial cooperation, they do not in themselves fully explain the persistence of mutualism. The partner choice hypothesis is not exclusive from the host sanctions hypothesis, as it is apparent that both of them are prevalent in the symbiotic relationship. [28]

Evolutionary history

The symbiosis between nitrogen fixing rhizobia and the legume family has emerged and evolved over the past 66 million years. [29] [30] Although evolution tends to swing toward one species taking advantage of another in the form of noncooperation in the selfish-gene model, management of such symbiosis allows for the continuation of cooperation. [31] When the relative fitness of both species is increased, natural selection will favor symbiosis.

To understand the evolutionary history of this symbiosis, it is helpful to compare the rhizobia-legume symbiosis to a more ancient symbiotic relationship, such as that between endomycorrhizae fungi and land plants, which dates back to almost 460 million years ago. [32]

Endomycorrhizal symbiosis can provide many insights into rhizobia symbiosis because recent genetic studies have suggested that rhizobia co-opted the signaling pathways from the more ancient endomycorrhizal symbiosis. [33] Bacteria secrete Nod factors and endomycorrhizae secrete Myc-LCOs. Upon recognition of the Nod factor/Myc-LCO, the plant proceeds to induce a variety of intracellular responses to prepare for the symbiosis. [34]

It is likely that rhizobia co-opted the features already in place for endomycorrhizal symbiosis because there are many shared or similar genes involved in the two processes. For example, the plant recognition gene SYMRK (symbiosis receptor-like kinase) is involved in the perception of both the rhizobial Nod factors as well as the endomycorrhizal Myc-LCOs. [35] The shared similar processes would have greatly facilitated the evolution of rhizobial symbiosis because not all the symbiotic mechanisms would have needed to develop. Instead, the rhizobia simply needed to evolve mechanisms to take advantage of the symbiotic signaling processes already in place from endomycorrhizal symbiosis.

Other diazotrophs

Many other species of bacteria are able to fix nitrogen (diazotrophs), but few are able to associate intimately with plants and colonize specific structures like legume nodules. Bacteria that do associate with plants include the actinomycete, Frankia , which form symbiotic root nodules in actinorhizal plants, although these bacteria have a much broader host range, implying the association is less specific than in legumes. [16] Additionally, several cyanobacteria like Nostoc are associated with aquatic ferns, Cycas , and Gunneras, although they do not form nodules. [36] [37]

Additionally, loosely associated plant bacteria, termed endophytes, have been reported to fix nitrogen in planta. [38] These bacteria colonize the intercellular spaces of leaves, stems, and roots in plants [39] but do not form specialized structures like rhizobia and Frankia. Diazotrophic bacterial endophytes have very broad host ranges, in some cases colonizing both monocots and dicots. [40]

Note

  1. As with many bacterium classifications, taxonomy work is still in progress as new genetic data and discoveries re-shuffle the existing phylogenetic tree

Related Research Articles

<span class="mw-page-title-main">Leghemoglobin</span> Phytoglobin

Leghemoglobin is an oxygen-carrying phytoglobin found in the nitrogen-fixing root nodules of leguminous plants. It is produced by these plants in response to the roots being colonized by nitrogen-fixing bacteria, termed rhizobia, as part of the symbiotic interaction between plant and bacterium: roots not colonized by Rhizobium do not synthesise leghemoglobin. Leghemoglobin has close chemical and structural similarities to hemoglobin, and, like hemoglobin, is red in colour. It was originally thought that the heme prosthetic group for plant leghemoglobin was provided by the bacterial symbiont within symbiotic root nodules. However, subsequent work shows that the plant host strongly expresses heme biosynthesis genes within nodules, and that activation of those genes correlates with leghemoglobin gene expression in developing nodules.

<i>Rhizobium</i> Genus of nitrogen-fixing bacteria

Rhizobium is a genus of Gram-negative soil bacteria that fix nitrogen. Rhizobium species form an endosymbiotic nitrogen-fixing association with roots of (primarily) legumes and other flowering plants.

Diazotrophs are bacteria and archaea that fix gaseous nitrogen in the atmosphere into a more usable form such as ammonia.

<i>Ensifer meliloti</i> Species of bacterium

Ensifer meliloti are an aerobic, Gram-negative, and diazotrophic species of bacteria. S. meliloti are motile and possess a cluster of peritrichous flagella. S. meliloti fix atmospheric nitrogen into ammonia for their legume hosts, such as alfalfa. S. meliloti forms a symbiotic relationship with legumes from the genera Medicago, Melilotus and Trigonella, including the model legume Medicago truncatula. This symbiosis promotes the development of a plant organ, termed a root nodule. Because soil often contains a limited amount of nitrogen for plant use, the symbiotic relationship between S. meliloti and their legume hosts has agricultural applications. These techniques reduce the need for inorganic nitrogenous fertilizers.

<span class="mw-page-title-main">Root nodule</span> Plant part

Root nodules are found on the roots of plants, primarily legumes, that form a symbiosis with nitrogen-fixing bacteria. Under nitrogen-limiting conditions, capable plants form a symbiotic relationship with a host-specific strain of bacteria known as rhizobia. This process has evolved multiple times within the legumes, as well as in other species found within the Rosid clade. Legume crops include beans, peas, and soybeans.

<span class="mw-page-title-main">Nod factor</span> Signaling molecule

Nod factors, are signaling molecules produced by soil bacteria known as rhizobia in response to flavonoid exudation from plants under nitrogen limited conditions. Nod factors initiate the establishment of a symbiotic relationship between legumes and rhizobia by inducing nodulation. Nod factors produce the differentiation of plant tissue in root hairs into nodules where the bacteria reside and are able to fix nitrogen from the atmosphere for the plant in exchange for photosynthates and the appropriate environment for nitrogen fixation. One of the most important features provided by the plant in this symbiosis is the production of leghemoglobin, which maintains the oxygen concentration low and prevents the inhibition of nitrogenase activity.

<span class="mw-page-title-main">Rhizosphere</span> Region of soil or substrate comprising the root microbiome

The rhizosphere is the narrow region of soil or substrate that is directly influenced by root secretions and associated soil microorganisms known as the root microbiome. Soil pores in the rhizosphere can contain many bacteria and other microorganisms that feed on sloughed-off plant cells, termed rhizodeposition, and the proteins and sugars released by roots, termed root exudates. This symbiosis leads to more complex interactions, influencing plant growth and competition for resources. Much of the nutrient cycling and disease suppression by antibiotics required by plants, occurs immediately adjacent to roots due to root exudates and metabolic products of symbiotic and pathogenic communities of microorganisms. The rhizosphere also provides space to produce allelochemicals to control neighbours and relatives.

Sharon Rugel Long is an American plant biologist. She is the Steere-Pfizer Professor of Biological Science in the Department of Biology at Stanford University, and the Principal Investigator of the Long Laboratory at Stanford.

Symbiotic bacteria are bacteria living in symbiosis with another organism or each other. For example, rhizobia living in root nodules of legumes provide nitrogen fixing activity for these plants.

Horizontal transmission is the transmission of organisms between biotic and/or abiotic members of an ecosystem that are not in a parent-progeny relationship. This concept has been generalized to include transmissions of infectious agents, symbionts, and cultural traits between humans.

<i>Bradyrhizobium</i> Genus of bacteria

Bradyrhizobium is a genus of Gram-negative soil bacteria, many of which fix nitrogen. Nitrogen fixation is an important part of the nitrogen cycle. Plants cannot use atmospheric nitrogen (N2); they must use nitrogen compounds such as nitrates.

Actinorhizal plants are a group of angiosperms characterized by their ability to form a symbiosis with the nitrogen fixing actinomycetota Frankia. This association leads to the formation of nitrogen-fixing root nodules.

Microbial inoculants also known as soil inoculants or bioinoculants are agricultural amendments that use beneficial rhizosphericic or endophytic microbes to promote plant health. Many of the microbes involved form symbiotic relationships with the target crops where both parties benefit (mutualism). While microbial inoculants are applied to improve plant nutrition, they can also be used to promote plant growth by stimulating plant hormone production. Although bacterial and fungal inoculants are common, inoculation with archaea to promote plant growth is being increasingly studied.

Bradyrhizobium japonicum is a species of legume-root nodulating, microsymbiotic nitrogen-fixing bacteria. The species is one of many Gram-negative, rod-shaped bacteria commonly referred to as rhizobia. Within that broad classification, which has three groups, taxonomy studies using DNA sequencing indicate that B. japonicum belongs within homology group II.

Ensifer fredii is a nitrogen fixing bacteria of the genus Sinorhizobium. It is a fast-growing root nodule bacteria. Sinorhizobium fredii exhibit a broad host-range and are able to nodulate both determinant hosts such as soy as well as indeterminate hosts including the pigeon pea. Because of their ease of host infection there is interest in their genetics and the symbiotic role in host infection and nodule formation.

Pararhizobium giardinii is a Gram negative root nodule bacteria. It forms nitrogen-fixing root nodules on legumes, being first isolated from those of Phaseolus vulgaris.

Mesorhizobium mediterraneum is a bacterium from the genus Mesorhizobium, which was isolated from root nodule of the Chickpea in Spain. The species Rhizobium mediterraneum was subsequently transferred to Mesorhizobium mediterraneum. This species, along with many other closely related taxa, have been found to promote production of chickpea and other crops worldwide by forming symbiotic relationships.

Martin Parniske is a German biologist with a specialisation in genetics, microbiology and biochemistry. He is university professor and head of the Institute of Genetics at the Faculty of Biology of the Ludwig Maximilian University of Munich. Parniske's scientific focus is on the molecular interaction between plants and symbiotic and pathogenic organisms including bacteria, fungi, oomycetes and insects.

<span class="mw-page-title-main">Symbiosome</span>

A symbiosome is a specialised compartment in a host cell that houses an endosymbiont in a symbiotic relationship.

Tripartite symbiosis is a type of symbiosis involving three species. This can include any combination of plants, animals, fungi, bacteria, or archaea, often in interkingdom symbiosis.

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Further reading