The Poaceae is one of the most important Angiosperm families, in terms of morphological diversity, ecology and economic importance. Species within this family show a very wide variation in terms of salinity tolerance. Salt secretion through salt glands plays a significant role in regulating ion balance, contributing to salinity tolerance. This review focuses on salt glands in the Poaceae family and their role in the salinity tolerance. In Poaceae microhairs have been observed in all subfamilies, except Pooideae, but functioning salt glands are reported only in genera belonging to the Chloridoideae subfamily. Structural, ultrastructural and physiological features of salt glands are summarized and discussed and the use of salt glands as potential target features for improving salt tolerance of crops is considered.

Cytosolic glyceraldehyde-3-phosphate dehydrogenase (NAD-GAPDH) is involved in a critical energetic step of glycolysis and also has many important functions besides its enzymatic activity. The recombinant wheat NAD-GAPDH was phosphorylated in vitro at Ser205 by a SNF1-Related protein kinase 1 (SnRK1) from wheat heterotrophic (but not from photosynthetic) tissues. The S205D mutant enzyme (mimicking the phosphorylated form) exhibited a significant decrease in activity but similar affinity toward substrates. Immunodetection and activity assays showed that NAD-GAPDH is phophorylated in vivo, the enzyme depicting different activity, abundance and phosphorylation profiles during development of seeds that mainly accumulate starch (wheat) or lipids (castor oil seed). NAD-GAPDH activity gradually increases along wheat seed development, but protein levels and phosphorylation status exhibited slight changes. Conversely, in castor oil seed, the activity slightly increased and total protein levels do not significantly change in the first half of seed development but both abruptly decreased in the second part of development, when triacylglycerols synthesis and storage begin. Interestingly, phospho-NAD-GAPDH levels reached a maximum when the seeds switch their metabolism to mainly support synthesis and accumulation of carbon reserves. After this point the castor oil seed NAD-GAPDH protein levels and activity highly decreased, and the protein stability assays showed that the protein would be degraded by the proteasome. The results presented herein suggest that phosphorylation of NAD-GAPDH during seed development would have impact on the partitioning of triose-phosphate between different metabolic pathways and cell compartments to support the specific carbon, energy and reducing equivalents demands during synthesis of storage products.

In many countries, Amaranthus hybridus is a widespread weed in agricultural systems. The high prolificacy and invasive capacity as well as the resistance of some biotypes to herbicides are among the complications of handling this weed. This paper reports on the first A. hybridus biotypes with resistance to auxinic herbicides and multiple resistance to auxinic herbicides and the EPSPs inhibitor, glyphosate. Several dose response assays were carried out to determine and compare sensitivity of six population of A. hybridus to glyphosate, 2,4-D, and dicamba. In addition, shikimic acid accumulation and piperonil butoxide effects on 2,4-D and dicamba metabolism were tested in the same populations. The results showed four populations were resistant to dicamba and three of these were also resistant to 2,4-D, while only one population was resistant to glyphosate. The glyphosate-resistant population also showed multiple resistance to auxinic herbicides. Pretreatment with piperonil butoxide (PBO) followed by 2,4-D or dicamba resulted in the death of all individual weeds independent of herbicide or population.

2,4-D resistance is increasing around the world due to both transgenic crops and resistance to other herbicides. The objective of the this study was to characterize the currently unknown mechanisms of 2,4-D resistance in five weed species from around the globe: Amaranthus hybridus (Argentina), Conyza canadensis (Hungary), Conyza sumatrensis (France), Hirschfeldia incana (Argentina) and Parthenium hysterophorus (Dominican Republic), using Papaver rhoeas (Spain) as a standard resistant (R) species. Dose-response trials using malathion and absorption, translocation and metabolism experiments were performed to unravel the resistance mechanisms. R plants produced at least 3-folds less ethylene than susceptible plants, confirming the resistance to 2,4-D, together with resistance factors >4. A. hybridus, P. hysterophorus and P. rhoeas showed both reduced translocation and enhanced metabolism. In the two Conyza sps., the only resistance mechanism found was enhanced metabolism. Malathion synergized with 2,4-D in all these species, indicating the role of cytochrome P450 in the herbicide degradation. In H. incana, reduced translocation was the only contributing mechanism to resistance. Among the six dicotyledonous weed species investigated, there was a differential contribution to 2,4-D resistance of enhanced metabolism and reduced translocation. Thus, extrapolating 2,4-D resistance mechanisms from one weed species to another is very risky, if even related.

The levels of resistance to glyphosate of 13 barnyard grass (Echinochloa crus-galli) populations harvested across different agriculture areas in the Southern Iberian Peninsula were determined in greenhouse and laboratory experiments. Shikimate accumulation fast screening separated the populations regarding resistance to glyphosate: susceptible (S) E2, E3, E4, and E6 and resistant (R) E1, E5, E7, E8, E9, E10, E11, E12, and E13. However, resistance factor (GR₅₀ E1–E13/GR₅₀ E6) values separated these populations into three groups: (S) E2, E3, E4, and E6, (R) E1, E5, E7, E8, and E9, and very resistant (VR) E10, E11, E12, and E13. ¹⁴C-glyphosate assays performed on two S populations (E2 and E6) showed greater absorption and translocation than those found for R (E7 and E9) and VR (E10 and E12) populations. No previous population metabolized glyphosate to amino methyl phosphonic acid (AMPA) and glyoxylate, except for the E10 population that metabolized 51% to non-toxic products. The VR populations showed two times more 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) activity without herbicide than the rest, while the inhibition of the EPSPS activity by 50% (I₅₀) required much higher glyphosate in R and VR populations than in S populations. These results indicated that different target-site and non-target-site resistance mechanisms were implicated in the resistance to glyphosate in E. crus-galli. Our results conclude that resistance is independent of climate, type of crop, and geographic region and that the level of glyphosate resistance was mainly due to the selection pressure made by the herbicide on the different populations of E. crus-galli studied.