scholarly journals Iron Transport across Symbiotic Membranes of Nitrogen-Fixing Legumes

2021 ◽  
Vol 22 (1) ◽  
pp. 432
Author(s):  
David A. Day ◽  
Penelope M. C. Smith

Iron is an essential nutrient for the legume-rhizobia symbiosis and nitrogen-fixing bacteroids within root nodules of legumes have a very high demand for the metal. Within the infected cells of nodules, the bacteroids are surrounded by a plant membrane to form an organelle-like structure called the symbiosome. In this review, we focus on how iron is transported across the symbiosome membrane and accessed by the bacteroids.

2015 ◽  
Vol 28 (5) ◽  
pp. 605-614 ◽  
Author(s):  
Aleksandr Gavrin ◽  
Veerle Jansen ◽  
Sergey Ivanov ◽  
Ton Bisseling ◽  
Elena Fedorova

The nitrogen-fixing rhizobia in the symbiotic infected cells of root nodules are kept in membrane compartments derived from the host cell plasma membrane, forming what are known as symbiosomes. These are maintained as individual units, with mature symbiosomes having a specific radial position in the host cell cytoplasm. The mechanisms that adapt the host cell architecture to accommodate intracellular bacteria are not clear. The intracellular organization of any cell depends heavily on the actin cytoskeleton. Dynamic rearrangement of the actin cytoskeleton is crucial for cytoplasm organization and intracellular trafficking of vesicles and organelles. A key component of the actin cytoskeleton rearrangement is the ARP2/3 complex, which nucleates new actin filaments and forms branched actin networks. To clarify the role of the ARP2/3 complex in the development of infected cells and symbiosomes, we analyzed the pattern of actin microfilaments and the functional role of ARP3 in Medicago truncatula root nodules. In infected cells, ARP3 protein and actin were spatially associated with maturing symbiosomes. Partial ARP3 silencing causes defects in symbiosome development; in particular, ARP3 silencing disrupts the final differentiation steps in functional maturation into nitrogen-fixing units.


1976 ◽  
Vol 194 (1116) ◽  
pp. 285-293 ◽  

In cross-inoculation trials, inocula containing the nodule endophytes of Myrica gale, M. cerifera, M. cordifolia and M. pilulifera respectively were applied to the roots of young plants of M. faya Ait. growing in nitrogen-free culture solution. All four inocula induced nodule formation, and except where the M. gale inoculum had been used the nodules were of effective type and enabled the plants bearing them to grow nearly as well as other M. faya plants associated with the normal endophyte. The nodules induced by the M. gale endophyte were very numerous, but remained small and fixed no significant amount of nitrogen, and were thus ineffective. Light and electron microscopy showed that in the effective nodules induced by the normal endophyte or by that of M. cordifolia , the endophyte was confined to a layer 1-2 cells deep near the middle of the nodule cortex, and that in respect of the width of the hyphae and their production of club-shaped internally subdivided vesicles, the endophytes resembled closely those in the nodules of the few other species of Myrica that have been studied by modern methods of microscopy. In ineffective nodules the disposition of the infected cells was unchanged, but within the cells only a sparse development of the endophyte was observed, and no vesicles were found. The finding that nodules lacking vesicles showed little or no fixation is consistent with other evidence that the vesicles normally produced by non-legume nodule endophytes are the main site of nitrogen fixation.


Author(s):  
T. Bisseling ◽  
R.C. Van Den Bos ◽  
M.W. Weststrate ◽  
M.J.J. Hakkaart ◽  
A. Van Kammen

1992 ◽  
Vol 38 (6) ◽  
pp. 526-533 ◽  
Author(s):  
A. B. M. Siddique ◽  
A. K. Bal

Nitrogen fixation in legume root nodules is believed to be supported by the supply of photosynthate of the current photoperiod. However, in peanut nodules, prolonged periods of darkness or detopping do not disrupt nitrogen fixation for at least 48 h. During this period, nodule oleosomes (lipid bodies) have been shown to decrease in number within the infected cells, and it has been suggested that lipids from oleosomes are mobilized to maintain the energy and carbon requirements of the nitrogen-fixing nodules. We present morphological evidence, at the ultrastructural level, for the utilization of oleosomes during photosynthate stress. The biochemical status of the nodule has also been assessed and correlated with ultrastructure. For comparison cowpea nodules were used that totally lacked oleosomes. In peanut nodules leghemoglobin and total protein remained unchanged along with integrated ultrastructure on nodule cells for 48 h, whereas in cowpea a decline in proteins with ultrastructural damage became apparent within a very short period of photosynthate stress. In peanut nodules empty or partially empty oleosomes were taken as evidence for their utilization during the stress period. Key words: N2 fixation, photosynthate stress, lipid bodies, catalase, malate synthase, peanut nodule, β-oxidation.


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