I. STUDIES FOCUSED ON THE PLANT PARTNER |
G. max roots (wt and SS2-2 mutant) |
B. japonicum USDA110 |
Lim et al., 2010
|
Protein-mediated suppression of defense-related responses in root cells upon inoculation with symbiotic bacteria. |
G. max root hairs |
B. japonicum USDA110 |
Wan et al., 2005
|
Induction of phospholipases, phosphoglucomutases, lectins, and an actin isoform in soybean roots upon B. japonicum inoculation. |
G. max nodules (cytosol fraction) |
B. japonicum USDA110 |
Oehrle et al., 2008
|
Proteins related to carbon and nitrogen metabolism, oxygen supply and protection are predominantly found in the cytosol of nodule cells. |
G. max En-b0-1 roots (supernodulating) |
B. japonicum MAFF 211342 |
Salavati et al., 2012
|
Identification of a correlation between the levels of a peroxidase isoform and nodulation at the protein but not transcript level in soybean nodules. |
L. japonicus roots and nodules |
M. loti MAFF30309 |
Dam et al., 2014
|
Establishment of 2D-PAGE reference maps of L. japonicum roots and nodules. |
M. alba nodules |
S. meliloti 1021 |
Natera et al., 2000
|
Identification of nearly 100 plant and bacterial proteins in white sweetclover nodules. |
M. truncatula roots |
S. meliloti 2011 |
Bestel-Corre et al., 2002
|
Two leghemoglobin isoforms and one enolase protein were accumulated in roots upon inoculation with symbiotic bacteria. |
M. truncatula nodules |
S. meliloti 2011 |
Larrainzar et al., 2007
|
Identification of 377 plant proteins in nodules, mostly related to amino acid metabolism and protein synthesis and degradation. |
M. truncatula nodules |
S. meliloti 2011 |
Larrainzar et al., 2009
|
Integrative proteomic and metabolomic analysis of the effects of drought stress in the plant and bacteroid fractions of M. truncatula nodules. |
M. truncatula roots and nodules |
S. meliloti 2011 |
Larrainzar et al., 2014
|
Absolute quantification proteomics and gene expression analyses show that sulfur metabolism and ethylene biosynthesis have key roles in the response of nodules and roots subjected to drought stress. |
M. truncatula shoots and roots |
S. meliloti 1021 |
Molesini et al., 2014
|
Analysis of local and systemic responses of M. truncatula roots and shoots upon inoculation. |
M. truncatula roots (wt and skl mutant) |
S. meliloti 1021 |
Prayitno et al., 2006
|
Increased abundance of one ACC oxidase isoform in wild-type roots but not in roots of the supernodulating skl mutant upon inoculation. |
M. truncatula roots and shoots |
S. meliloti 2011 |
Staudinger et al., 2012
|
Detection of salt and drought stress markers and identification of an improved plant response to stress of plants grown under symbiotic conditions when compared to nitrate-fed plants. |
M. truncatula shoots |
S. medicae WSM419 and S. meliloti 2011 |
Staudinger et al., 2016
|
Plants grown under symbiotic conditions present reduced levels of leaf senescence during drought stress independently of the efficiency of the symbiotic Rhizobium strain used. |
P. sativum shoots |
R. leguminosarum bv. viciae
|
Irar et al., 2014
|
Identification of variations in protein abundance as part as the local responses of pea nodules grown under split-root conditions and subjected to water stress. |
P. sativum shoots (soluble and plasma membrane fractions) |
R. leguminosarum bv. viciae
|
Desalegn et al., 2016
|
Indications of a positive influence of the symbiotic interaction on the activation of the plant defense responses upon pathogen attack. |
P. sativum shoots |
R. leguminosarum bv. viciae
|
Turetschek et al., 2016
|
Proteomic and metabolomic analyses of two pea cultivars with varying pathogen resistance levels associate tolerance to ethylene biosynthesis and suppression of cell death responses. |
V. unguiculata roots |
Rhizobium sp. NGR234 |
Krause and Broughton, 1992
|
One of the first proteomic studies analyzing symbiosis-specific proteins potentially involved in root-hair deformation in cowpea. |
II. STUDIES FOCUSED ON THE
Rhizobium
PARTNER
|
B. japonicum USDA110 |
Bacteroids |
Sarma and Emerich, 2005
|
Abundance of proteins related to nitrogen and carbon metabolism, and transport in soybean nodule bacteroids. |
B. japonicum USDA110 |
Free-living cells vs. bacteroids |
Sarma and Emerich, 2006
|
Compared to bacteria under free-living conditions, nodule bacteroids present unusually low levels in proteins related to fatty acid and nucleic acid metabolism. |
B. japonicum USDA110 |
Bacteroids |
Delmotte et al., 2010
|
In contrast to previous reports, application of more sensitive LC-MS/MS-based approaches identifies a complete set of proteins related to de novo nucleoside and nucleotide biosynthesis in bacteroids. |
Bradyrhizobium sp. ORS278 |
Bacteroids (Aeschynomene indica root and stem nodules) |
Delmotte et al., 2014
|
Root and stem nodule bacteroids show expression of similar sets of proteins, mostly related to central metabolism. As exceptions, proteins involved in photosynthesis were exclusive found in stem nodules. |
M. loti MAFF30309 |
Free-living cells vs. bacteroids |
Tatsukami et al., 2013
|
Differentiated bacteroids do not longer express proteins either involved in peptidoglycan biosynthesis or proteins related to the flagellum. |
M. loti MAFF30309 |
Bacteroids |
Nambu et al., 2015
|
Time-course analysis of nodulation suggests that bacteroids experience nitrogen-deficiency at early stages of nodule development. |
S. meliloti 1021 |
Free-living cells vs. bacteroids |
Djordjevic et al., 2003
|
Compared to free-living bacteria, nodule bacteroids appear not to require the expression of sugar transporters or enzymes involved in the early steps of glycolysis. |
S. meliloti 1021 |
Bacteroids |
Djordjevic, 2004
|
Bacteroids express a specific set of ABC-type transporters involved in the transport of amino acids and inorganic ions. |