Histochemical techniques in plant science: more than meets the eye

Author(s):  
Vaishali Yadav ◽  
Namira Arif ◽  
Vijay Pratap Singh ◽  
Gea Guerriero ◽  
Roberto Berni ◽  
...  

Abstract Histochemistry is an essential analytical tool interfacing extensively with plant science. The literature is indeed constellated with examples showing its use to decipher specific physiological and developmental processes, as well as to study plant cell structures. Plant cell structures are translucent unless they are stained. Histochemistry allows the identification and localization, at the cellular level, of biomolecules and organelles in different types of cells and tissues, based on the use of specific staining reactions and imaging. Histochemical techniques are also widely used for the in-vivo localization of promoters in specific tissues, as well as to identify specific cell wall components such as lignin and polysaccharides. Histochemistry also enables the study of plants’ reactions to environmental constraints, for example, the production of reactive oxygen species (ROS) can be traced by applying histochemical staining techniques. The possibility of detecting ROS and localizing them at the cellular level is vital in establishing the mechanisms involved in the sensitivity and tolerance to different stress conditions in plants. This review comprehensively highlights the additional value of histochemistry as a complementary technique to high-throughput approaches for the study of the plant response to environmental constraints. Moreover, here we have provided and extensive survey of the available plant histochemical staining methods used for the localization of metals, minerals, secondary metabolites, cell wall components, as well as the detection of ROS production in plant cells. The use of recent technological advances like CRISPR/Cas9 based genome-editing for histological application is also addressed. This review also surveys the availale literature data on histochemical techniques used to study the response of plants to abiotic stresses and to identify the effects at the tissue and cell-level.

Author(s):  
WILLIAM S. YORK ◽  
ALAN G. DARVILL ◽  
MICHAEL MCNEIL ◽  
THOMAS T. STEVENSON ◽  
PETER ALBERSHEIM

Author(s):  
William S. York ◽  
Alan G. Darvill ◽  
Michael McNeil ◽  
Thomas T. Stevenson ◽  
Peter Albersheim

2017 ◽  
Vol 233 ◽  
pp. 216-227 ◽  
Author(s):  
Anh Dao T. Phan ◽  
Bernadine M. Flanagan ◽  
Bruce R. D'Arcy ◽  
Michael J. Gidley

2013 ◽  
Vol 6 (3) ◽  
pp. 898 ◽  
Author(s):  
Jaclyn D. DeMartini ◽  
Sivakumar Pattathil ◽  
Jeffrey S. Miller ◽  
Hongjia Li ◽  
Michael G. Hahn ◽  
...  

2015 ◽  
Vol 3 (1) ◽  
pp. 56-72 ◽  
Author(s):  
Yogesh K. Murugesan ◽  
Damiano Pasini ◽  
Alejandro D. Rey

2016 ◽  
Vol 82 (17) ◽  
pp. 5174-5185 ◽  
Author(s):  
Elena Geiser ◽  
Michèle Reindl ◽  
Lars M. Blank ◽  
Michael Feldbrügge ◽  
Nick Wierckx ◽  
...  

ABSTRACTThe microbial conversion of plant biomass to valuable products in a consolidated bioprocess could greatly increase the ecologic and economic impact of a biorefinery. Current strategies for hydrolyzing plant material mostly rely on the external application of carbohydrate-active enzymes (CAZymes). Alternatively, production organisms can be engineered to secrete CAZymes to reduce the reliance on externally added enzymes. Plant-pathogenic fungi have a vast repertoire of hydrolytic enzymes to sustain their lifestyle, but expression of the corresponding genes is usually highly regulated and restricted to the pathogenic phase. Here, we present a new strategy in using the biotrophic smut fungusUstilago maydisfor the degradation of plant cell wall components by activating its intrinsic enzyme potential during axenic growth. This fungal model organism is fully equipped with hydrolytic enzymes, and moreover, it naturally produces value-added substances, such as organic acids and biosurfactants. To achieve the deregulated expression of hydrolytic enzymes during the industrially relevant yeast-like growth in axenic culture, the native promoters of the respective genes were replaced by constitutively active synthetic promoters. This led to an enhanced conversion of xylan, cellobiose, and carboxymethyl cellulose to fermentable sugars. Moreover, a combination of strains with activated endoglucanase and β-glucanase increased the release of glucose from carboxymethyl cellulose and regenerated amorphous cellulose, suggesting that mixed cultivations could be a means for degrading more complex substrates in the future. In summary, this proof of principle demonstrates the potential applicability of activating the expression of native CAZymes from phytopathogens in a biocatalytic process.IMPORTANCEThis study describes basic experiments that aim at the degradation of plant cell wall components by the smut fungusUstilago maydis. As a plant pathogen, this fungus contains a set of lignocellulose-degrading enzymes that may be suited for biomass degradation. However, its hydrolytic enzymes are specifically expressed only during plant infection. Here, we provide the proof of principle that these intrinsic enzymes can be synthetically activated during the industrially relevant yeast-like growth. The fungus is known to naturally synthesize valuable compounds, such as itaconate or glycolipids. Therefore, it could be suited for use in a consolidated bioprocess in which more complex and natural substrates are simultaneously converted to fermentable sugars and to value-added compounds in the future.


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