ROLE OF ALKYLRESORCINOLS IN COLONIZATION OF WHEAT BY PSEUDOMONAS SP. STRAIN 150

Author(s):  
Elżbieta G. Magnucka ◽  
◽  
Stanisław J. Pietr ◽  
Keyword(s):  
2020 ◽  
Vol 23 ◽  
pp. 03009
Author(s):  
Maxim. D. Timergalin ◽  
Arina V. Feoktistova ◽  
Timur V. Rameev ◽  
Gaisar G. Khudaygulov ◽  
Sergei N. Starikov ◽  
...  

This article submits results of laboratory and field experiments on the effect of an auxin-producing bacterial strain Pseudomonas sp. DA1.2 in comparison with Pseudomonas koreensis IB-4 on wheat plants in conjunction with the “Chistalan” herbicide treatment. Our work shows the positive effect of bacterial treatments on plant growth, the relative water content in leaves and the role of bacteria in the redistribution of ABA and IAA in wheat shoots under conditions of herbicidal stress. Application of Pseudomonas sp. DA1.2 together with the herbicide in the field of the steppe zone led to an increase in yield by 20% relative to the control variant. This bacterial strain helps to overcome herbicidal stress and is a promising agent for improving the technology of using synthetic auxins herbicides.


Microbiology ◽  
2005 ◽  
Vol 151 (5) ◽  
pp. 1403-1408 ◽  
Author(s):  
Daan van den Broek ◽  
Thomas F. C. Chin-A-Woeng ◽  
Guido V. Bloemberg ◽  
Ben J. J. Lugtenberg

Pseudomonas sp. strain PCL1171 undergoes reversible colony phase variation between opaque phase I and translucent phase II colonies, which is dependent on spontaneous mutations in the regulatory genes gacA and gacS. Mutation of the mutS gene and constitutive expression of rpoS increases the frequency at which gac mutants appear 1000- and 10-fold, respectively. Experiments were designed to study the relationship between gacS, rpoS and mutS. These studies showed that (i) a functional gac system is required for the expression of rpoS, (ii) RpoS suppresses the expression of mutS and therefore increases the frequency of gac mutants, and (iii) upon mutation of rpoS and gacS, the expression of mutS is increased. Mutation of gacS abolishes suppression of mutS expression in stationary growth, suggesting that additional gac-dependent factors are involved in this suppression. In conclusion, inefficient mutation repair via MutS, of which the expression is influenced by gacA/S itself and by rpoS in combination with other factors, contributes to the high frequency of mutations accumulating in gacA/S. The role of RpoS in the growth advantage of a gac mutant was analysed, and mutation of rpoS only reduced the length of the lag phase, but did not affect the growth rate, suggesting a role for both RpoS and a reduction of metabolic load in the growth advantage of a gac mutant.


2019 ◽  
Vol 31 (9) ◽  
pp. 1507 ◽  
Author(s):  
Núria Arcarons ◽  
Meritxell Vendrell-Flotats ◽  
Marc Yeste ◽  
Elena Mercade ◽  
Manel López-Béjar ◽  
...  

Biological molecules isolated from organisms that live under subzero conditions could be used to protect oocytes from cryoinjuries suffered during cryopreservation. This study examined the cryoprotectant role of exopolysaccharides of Pseudomonas sp. ID1 (EPS ID1) in the vitrification of prepubertal and adult cow oocytes. IVM oocytes were vitrified and warmed in media supplemented with 0, 1, 10, 100 or 1000µgmL−1 EPS ID1. After warming, oocytes were fertilised and embryo development, spindle morphology and the expression of several genes in Day 8 blastocysts were assessed. Vitrification led to significantly lower proportion of prepubertal oocytes exhibiting a normal spindle configuration. In fresh control oocytes and most groups of vitrified adult oocytes, similar percentages of oocytes with a normal spindle configuration were observed. Percentages of Day 8 blastocysts were similar for prepubertal oocytes vitrified in the absence or presence of 1 or 10µgmL−1 EPS ID1 and for adult oocytes vitrified in the presence of 10µgmL−1 EPS ID1 compared with non-vitrified oocytes. EPS ID1 supplementation had no effect on solute carrier family 2 member 3 (SLC2A3), ubiquitin-conjugating enzyme E2A (UBE2A) and histone deacetylase 1 (HDAC1) expression in Day 8 blastocysts form adult oocytes. However, supplementation with 10 and 100µgmL−1 EPS ID1 led to increased expression of genes involved in epigenetic modifications (DNA methyltransferase 3 alpha (DNMT3A) and K (lysine) acetyltransferase 2A (KAT2A)) and apoptosis (BCL2 associated X apoptosis regulator (BAX) and BCL2-like 1 (BCL2L1)). The lowest BAX:BCL2L1 ratio was found in the 10µgmL−1 EPS ID1-supplemented group. The results suggest that 10µgmL−1 EPS ID1 added to vitrification and warming media may help protect bovine oocytes against cryodamage.


2014 ◽  
Vol 52 (12) ◽  
pp. 1020-1024 ◽  
Author(s):  
Jian Zhang ◽  
Liyuan Meng ◽  
Yuanyuan Cao ◽  
Huiping Chang ◽  
Zhongyou Ma ◽  
...  

2007 ◽  
Vol 93 (3) ◽  
pp. 285-296 ◽  
Author(s):  
Reeta Davis ◽  
Arun Chandrashekar ◽  
Tumkur R. Shamala
Keyword(s):  

2005 ◽  
Vol 52 (7) ◽  
pp. 63-68 ◽  
Author(s):  
T.C. Lau ◽  
X.A. Wu ◽  
H. Chua ◽  
P.Y. Qian ◽  
P.K. Wong

Pseudomonas sp. CU-1, which was isolated from an interfacial biofilm of a sludge sample collected from an electroplating company, had a relatively high ability to adsorb Cu2 +  in solution. The bacterium grown in broth culture produced a large amount of capsular exopolymers mainly consisting of polysaccharides. The exopolysaccharides (EPS) were partially purified. The adsorption isotherm experiments showed that cells and EPS of Pseudomonas sp. CU-1 had similar Q0 and b for the dye, Janus Green, and Cu2+. The adsorption of Cu2 +  by cells could be monitored by the amount of dye displaced, due to the binding of metal ions onto the cell surface. The order of adsorption ability of metal ions and dye displacement by metal ion of the bacterium was: Cu2 + > Cd2 + > Zn2 + > Ni2 + . The results of the dye displacement by metal ions binding onto the surfaces of cells, EPS-removed cells, and EPS suggest that EPS produced by Pseudomonas sp. CU-1 plays an important role in preventing metal ions in the surrounding environment from contact with the bacterial cells. The possible role of the metal ion adsorption by the EPS of this biofilm bacterium was discussed.


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