Strigolactones (SLs) are multifunctional plant metabolites working not only as allelochemicals in the rhizosphere, but also as a novel class of hormones regulating growth and development in planta. To date, more than 30 SLs have been characterized, but the reason why plants produce structurally diverse SLs and the details of their biosynthetic pathway remain elusive. Recent studies using transcriptomics and reverse genetic techniques have paved the way to clarify the entire biosynthetic pathway of structurally diverse SLs. In this review, we discuss how various SLs are synthesized and what SL structural diversity means for plant growth and development.

Strigolactones (SLs) regulate important aspects of plant growth and stress responses. Many diverse types of SL occur in plants, but a complete picture of biosynthesis remains unclear. In Arabidopsis thaliana, we have demonstrated that MAX1, a cytochrome P450 monooxygenase, converts carlactone (CL) into carlactonoic acid (CLA) and that LBO, a 2‐oxoglutarate‐dependent dioxygenase, can convert methyl carlactonoate (MeCLA) into a metabolite called [MeCLA + 16 Da]. In the present study, feeding experiments with deuterated MeCLAs revealed that [MeCLA + 16 Da] is hydroxymethyl carlactonoate (1'‐HO‐MeCLA). Importantly, this LBO metabolite was detected in plants. Interestingly, other related compounds, methyl 4‐hydroxycarlactonoate (4‐HO‐MeCLA) and methyl 16‐hydroxycarlactonoate (16‐HO‐MeCLA), were also found to accumulate in lbo mutants. 3‐HO‐, 4‐HO‐, and 16‐HO‐CL were detected in plants, but their expected corresponding metabolites, HO‐CLAs, were absent in max1 mutants. These results suggest that HO‐CL derivatives may be predominant SLs in Arabidopsis, produced through MAX1 and LBO.

Strigolactones (SLs) are essential host recognition signals for both root-parasitic plants and arbuscular mycorrhizal (AM) fungi in the rhizosphere, and in planta SLs or their metabolites function as a novel class of plant hormones that regulate various aspects of plant growth through crosstalk with other hormones. Although nutrient availability is one of the important factors influencing SL production and exudation, and phosphate (Pi) deficiency significantly promotes SL production and exudation in host plants of AM fungi, how nutrient availability modulates SL production and exudation remains elusive. Cytokinin (CK), a canonical plant hormone, has extensively been studied as a shoot branching promoter and its biosynthesis is also influenced by mineral nutrients, especially nitrate, indicating that CK might be another key factor that affect SL production and exudation. In the present study, we show that CKs (t-zeatin, benzyladenine, kinetin, and CPPU) applied to hydroponic culture media significantly suppressed the SL levels in both the root exudates and the root tissues of rice plants grown under Pi deficiency. In a split-root system, CK suppressed SL production locally, while Pi affected SL production systemically, suggesting that Pi and CK act on SL production independently in rice plants.

Strigolactones (SLs), a group of plant secondary metabolites, play an important role as a host recognition signal for symbiotic arbuscular mycorrhizal (AM) fungi in the rhizosphere. SLs promote symbioses with other beneficial microbes, including root nodule bacteria. Root parasitic weeds also take advantage of SLs as a clue to locate living host roots. In plants, SLs function as plant hormones regulating various growth and developmental processes including shoot and root architectures. Plants under nutrient deficiencies, especially that of phosphate, promote SL production and exudation to attract symbionts and to optimize shoot and root architecture.