Tangerine tomato roots show increased accumulation of acyclic carotenoids, less abscisic acid, drought sensitivity, and impaired endomycorrhizal colonization

Previously described methods to quantify the proportion of root length colonized by vesicular-arbuscular (VA) mycorrhizal fungi are reviewed. It is argued that these methods give observer-dependent measures of colonization which cannot be used to compare, quantitatively, roots examined by different researchers. A modified method is described here to estimate VA mycorrhizal colonization on an objective scale of measurement, involving inspection of intersections between the microscope eyepiece crosshair and roots at magnification × 200; it is referred to as the magnified intersections method. Whether the vertical eyepiece crosshair crosses one or more arbuscules is noted at each intersection. The estimate of colonization is the proportion of root length containing arbuscules, called the arbuscular colonization (AC). The magnified intersections method also determines the proportion of root length containing vesicles, the vesicular colonization (VC), and the proportion of root length containing hyphae, the hyphal colonization (HC). However, VC and HC should be interpreted with caution because vesicles and hyphae, unlike arbuscules, can be produced in roots by non-mycorrhizal fungi.

Strigolactones (SLs) are carotenoid-derived plant hormones and signaling molecules. When released into the soil, SLs indicate the presence of a host to symbiotic fungi and root parasitic plants. In planta, they regulate several developmental processes that adapt plant architecture to nutrient availability. Highly branched/tillered mutants in Arabidopsis, pea, and rice have enabled the identification of four SL biosynthetic enzymes: a cis/trans-carotene isomerase, two carotenoid cleavage dioxygenases, and a cytochrome P450 (MAX1). In vitro and in vivo enzyme assays and analysis of mutants have shown that the pathway involves a combination of new reactions leading to carlactone, which is converted by a rice MAX1 homolog into an SL parent molecule with a tricyclic lactone moiety. In this review, we focus on SL biosynthesis, describe the hormonal and environmental factors that determine this process, and discuss SL transport and downstream signaling as well as the role of SLs in regulating plant development.

We developed a reliable, inexpensive, and simple method for staining arbuscular-mycorrhizal fungal colonizations in root tissues. Apart from applications in research, this nontoxic, high-quality staining method also could be of great utility in teaching exercises. After adequate clearing with KOH, an ink-vinegar solution successfully stained all fungal structures, rendering them clearly visible.