scholarly journals Genes control of rates development as components of regulation stability of Triticum aestivum L. to biotic stress under conditions in vitro

Author(s):  
O. O. Avksentiieva ◽  
N. V. Terentiieva

Aim. The aim of our work is to research the influence of exometabolites phytopathogens of genus Fusarium on callus culture isogenic lines for genes PPD (NILs) of winter soft wheat. Methods. In the work used standard biotechnological and mycological methods. The influence of exometabolites phytopathogens g. Fusarium investigated, adding CF mi-cromycetes to MS culture medium in a ratio of 1:20, using transplants callus culture of isogenic lines of wheat. Growth index analyzed density of callus tissue and size of callus cells determined. Results. Established that the CF of Fusarium oxysporum significantly slows grows reaction of callus cultures and morphological structure callus NILs is changes. It is shown that the impact exometabolites phytopathogens has the opposite effect on cytological parameters (number and length callus cells) in the isolines differing pace of development in conditions in vivo. The culture filtrate F. oxysporum has more toxicity compared to exometabolites F. moniliforme. Conclusions. It is supposed that the genetic system controlling the pace of development and photoperiodic sensitivity Triticum aestivum L. in conditions in vivo indirectly determines the formation of resistance to biotic stress conditions in vitro. Keywords: Triticum aestivum L., Fusarium oxysporum, Fusarium moniliforme, PPD genes, NILs, callus culture, growth index, resistance to phytopathogens.

Author(s):  
Rizwan Sheirdil ◽  
Rifat Hayat ◽  
Xiao-Xia Zhang ◽  
Nadeem Abbasi ◽  
Safdar Ali ◽  
...  

Plant growth promoting rhizobacteria (PGPR) are capable to reduce the use of chemical fertilizers input cost of farmer. Keeping in view the study was designed to investigate and evaluate inoculation effect of indigenous rhizospheric bacteria on growth and yield of wheat (Triticum aestivum L.) under in vitro and in vivo conditions using different treatments. Ten potential strains were selected on the basis of their ACC deaminase activity, siderophore production, P-solubilization and production of indole acetic acid (IAA). Further these strains were tested in three different experiments (growth chamber, pot and field). We found significant increase in crop growth response to the inoculants in comparison with un-inoculated control. In pot and field trial we tested PGPR with recommended dose of inorganic fertilizers. The results of present study revealed that inoculation of bacterial strains with wheat seeds significantly increased plant growth and improved crop yield. Results of present study reveal that these strains could be employed in different combinations and can get higher yield in case of half recommended doses of inorganic fertilizers along with consortium of strains in comparison with sole application of recommended dose of fertilizer and with consortium of strains. These strains were further identified by 16Sr RNA gene sequencing, fatty acid profile and biolog. It can be concluded that inoculated bacteria have more potential and contributes in good crop quality, increased yield when they are applied in combination, thus have potential to minimize use of chemical fertilizers.


2006 ◽  
Vol 33 (7) ◽  
pp. 685 ◽  
Author(s):  
Aravind K. Jukanti ◽  
Phil L. Bruckner ◽  
Andreas M. Fischer

Polyphenol oxidases (PPOs) have been implicated in plant defence reactions. From an applied point of view, high PPO activity is associated with browning / darkening of fresh and processed food. Owing to its complex genome and economic importance, wheat (Triticum aestivum L.) represents an interesting system to advance our understanding of plant PPO function. We have previously shown that wheat PPOs are organised in a multigene family, consisting of two distinct phylogenetic clusters with three members each. In this study, we demonstrate that members of one cluster are not expressed in developing kernels or senescing flag leaves. Transcriptional regulation of one major gene in the other cluster largely controls PPO levels in these tissues, at least in the wheat varieties used for this study. Our data further indicate that the product of this gene is present as a latent enzyme during early kernel development, and that the latent enzyme is activated during later developmental phases. Enzyme activation can be achieved in vitro by limited tryptic digestion, but our data do not indicate activation by a proteolytic mechanism in vivo. Together, results presented in this study provide important insights into the regulation of wheat PPO function.


1969 ◽  
Vol 47 (8) ◽  
pp. 1334-1336 ◽  
Author(s):  
W. G. Barker

Explants derived from widely divergent tissues within the body of the basswood, Tilia americana L. (ovary wall, root and shoot cambia, perimedullary region, petiole), have the same general appearance when growing as a callus culture on identical media. The cambial-derived calli will meld into a single unit when placed in contact in the same culture bottle. Similarly, calli from several sources of wheat, Triticum aestivum L., are indistinguishable in vitro.From the standpoint of purely observational criteria, parenchyma explanted from several organs within the same organism responds in a seemingly identical way to the cultural environment.


2016 ◽  
Vol 24 (1) ◽  
pp. 222-229 ◽  
Author(s):  
O. O. Aksentyeva ◽  
V. V. Shulik

The article investigates the effects of the main manifestations of the genetic system controlling the type and rate of wheat development – VRN (vernalization) at the level of an integrated system of plant organism in vivo and callus certain population of cells in vitro. The paper studies the system of allelic VRN genes, which determine the need or insensitivity Triticum aestivum L. to vernalization and predetermination process of callusogenesis by the present system in vitro. In the experiments the modern model system of nearly isogenic lines (NILs) of spring type was used. The NILs were created in genotypes of the winter varieties Myronivska 808 and Olvia. Molecular genetic analysis of allelic loci of VRN genes was carried out by PCR analysis on grains and secondary callus culture using five pairs of specific primers (Grain Gene Mass Wheat). In the course of the experiments, it was found that the genetic system controlling the wheat rate determined the frequency of callusogenesis. However, the studied genetic system did not affect the morphological characteristics of primary and secondary callus tissue. In both hexaploid wheat cultivars the maximum frequency of callusogenesis appeared to be characterized in the Vrn 2 isogenic line and the original variety, slowly developing and intensely accumulating vegetative mass in vivo. The minimal frequency of callusogenesis was determined in the VRN 1 and VRN 3 isogenic lines, characterized by the rapid development of vegetation. The callus was derived from immature wheat embryos by morphological features analysis. Calluses with low water content, mainly, amorphous, compact, transparent, white or with yellowish tint were identified. Using PCR analysis, in grains in vivo and in the callus culture in vitro the almost identical allelic status of VRN genes was revealed. In grains and callus of Vrn 1 isogenic lines of both wheat varieties the presence of a dominant gene VRN A1 and recessive VRN B1 and VRN D1 was detected, whereas in VRN 2 – a dominant gene VRN B1 and recessive VRN A1 and VRN D1. However, the dominant allele VRN D1 in the studied NILs was detected. Therefore, in varieties of grains and callus cultures all genes are represented only by recessive alleles VRN A1, VRN B1 and VRN D1. Differences were found in the callus culture of VRN 3 isogenic line of Myronivska 808 on the allelic state of theVRN B1 gene. The obtained results could be associated with genomic reconstructions during callusogenesis induction. Our studies indicate the unidirectional system of VRN genes functioning, which appears to be the main control system of type and rate of soft wheat development in the system in vivo and in vitro. This allows us to assume the role of the VRN genetic system in the determination of callusogenesis, and also the adequacy of the functioning of the system in vitro processes, determining the system of integration of plants. Thus, our study confirms that the callus tissues cells of higher plants are able to preserve the cells properties of the whole organism along with the acquisition of new specific properties. Moreover, the culture in vitro is an adequate system for the study of the plant organism properties as a system.


Sign in / Sign up

Export Citation Format

Share Document