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8,540 result(s) for "Cytokinins"
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Effects of 6-Benzylaminopurine Combined with Prohexadione-Ca on Yield and Quality of IChrysanthemum morifolium/I Ramat cv. Hangbaiju
Increasing shoot branch numbers of Chrysanthemum morifolium Ramat cv. Hangbaiju (Hangbaiju) is crucial for producing high flower yields. Pot experiments were designed to evaluate the effects of foliar application of 6-benzylaminopurine (6-BA) combined with prohexadione-Ca (Pro-Ca) on the yield and quality of Hangbaiju flowers. Foliar application of 6-BA combined with Pro-Ca typically increased leaf chlorophyll content and decreased leaf soluble sugar and soluble protein contents throughout the floral organ growth phase. At the bud formation phenophase stage (August), the contents of gibberellin (GA), indole-3-acetic acid (IAA), and zeatin (ZA) decreased (except for GA content in the 10 mg L[sup.−1] 6-BA combined with 100 mg L[sup.−1] Pro-Ca treatment), but abscisic acid (ABA) content increased. The yield of Hangbaiju flowers was found higher in plants treated with foliar application of 6-BA combined with Pro-Ca. Higher yields were found in the 6-BA[sub.5] + Ca[sub.100] and 6-BA[sub.10] + Ca[sub.100] treatments than in the 6-BA[sub.5] + Ca[sub.50] and 6-BA[sub.10] + Ca[sub.50] treatments, and the highest yield was observed in the 6-Ba[sub.5] + Ca[sub.100] treatment both in 2019 and 2020. Nutritional indices such as soluble sugar, soluble protein, total amino acid, and water extract increased, and medicinal indices such as flavonoid, total phenolics, chlorogenic acid, cynaroside, and 3,5-dicaffeoyl quinic acid slightly decreased after foliar application of 6-BA combined with Pro-Ca; however, they were all higher than the standards recorded in the Chinese Pharmacopeia. Overall, foliar application of 6-BA combined with Pro-Ca could increase the yield and nutritional quality of Hangbaiju flowers, enhancing its tea quality.
Evolution of cytokinin biosynthesis and degradation
Cytokinin hormones are important regulators of development and environmental responses of plants that execute their action via the molecular machinery of signal perception and transduction. The limiting step of the whole process is the availability of the hormone in suitable concentrations in the right place and at the right time to interact with the specific receptor. Hence, the hormone concentrations in individual tissues, cells, and organelles must be properly maintained by biosynthetic and metabolic enzymes. Although there are merely two active cytokinins, isopentenyladenine and its hydroxylated derivative zeatin, a variety of conjugates they may form and the number of enzymes/isozymes with varying substrate specificity involved in their biosynthesis and conversion gives the plant a variety of tools for fine tuning of the hormone level. Recent genome-wide studies revealed the existence of the respective coding genes and gene families in plants and in some bacteria. This review summarizes present knowledge on the enzymes that synthesize cytokinins, form cytokinin conjugates, and carry out irreversible elimination of the hormones, including their phylogenetic analysis and possible variations in different organisms.
Gynogenesis Induction in Sugar Beet and Synergized with Cold Pretreatment
For sugar beet (Beta vulgaris) breeding, producing homozygous lines through haploid and doubled haploid techniques are preferred over conventional and time-consuming methods. Doubled haploid sugar beet production necessitates inducing ovules to develop into haploid plants, referred to as gynogenesis. The protocol involves an interaction between cold pretreatment of six genotypes of sugar beet inflorescences at 4 °C for 1 week or more and 6-benzylaminopurine (BAP) concentrations (1 or 2 mg L.sup.-1) to increase the response rate of haploid embryo induction. Compared with freshly cultured ovules (6.49%), cold pretreatment for 1 week almost doubled the mean of haploid plantlet induction rate (11.3%), whereas pretreatment for more than 1 week was not as effective as the control. Addition of 2 mg L.sup.-1 BAP to the culture medium nearly doubled the induction rate of the cultured ovules (10.75%), followed by 1 mg L.sup.-1 BAP (7.78%) in comparison with hormone-free medium (5.69%). The highest gynogenesis rate (37.8%) was achieved when ovules were cultured on medium containing 2 mg L.sup.-1 BAP following 1-week cold pretreatment. This combination approximately tripled the mean total haploid embryo induction rate of all the genotypes to 16.3% in comparison with the control (5.74%). However, the addition of BAP resulted in vitrification proportionately. As a result, 2 mg L.sup.-1 BAP decreased the normal plantlet emergence (NPE) to one-third (7.59%) while 1 mg L.sup.-1 BAP had a moderate effect (NPE: 18.98%) in comparison with hormone-free treatment (NPE: 24.35%). The results indicate that the combination of cold pretreatment and BAP is very effective in inducing haploid plants from recalcitrant genotypes of sugar beet, but BAP can have both advantages and disadvantages.
The Hulks and the Deadpools of the Cytokinin Universe: A Dual Strategy for Cytokinin Production, Translocation, and Signal Transduction
Cytokinins are plant hormones, derivatives of adenine with a side chain at the N6-position. They are involved in many physiological processes. While the metabolism of trans-zeatin and isopentenyladenine, which are considered to be highly active cytokinins, has been extensively studied, there are others with less obvious functions, such as cis-zeatin, dihydrozeatin, and aromatic cytokinins, which have been comparatively neglected. To help explain this duality, we present a novel hypothesis metaphorically comparing various cytokinin forms, enzymes of CK metabolism, and their signalling and transporter functions to the comics superheroes Hulk and Deadpool. Hulk is a powerful but short-lived creation, whilst Deadpool presents a more subtle and enduring force. With this dual framework in mind, this review compares different cytokinin metabolites, and their biosynthesis, translocation, and sensing to illustrate the different mechanisms behind the two CK strategies. This is put together and applied to a plant developmental scale and, beyond plants, to interactions with organisms of other kingdoms, to highlight where future study can benefit the understanding of plant fitness and productivity.
Cytokinin glucosyl transferases, key regulators of cytokinin homeostasis, have potential value for wheat improvement
Summary The cytokinins, which are N6‐substituted adenine derivatives, control key aspects of crop productivity. Cytokinin levels are controlled via biosynthesis by isopentenyl transferase (IPT), destruction by cytokinin oxidase/dehydrogenase (CKX), and inactivation via glucosylation by cytokinin glucosyl transferases (CGTs). While both yield components and tolerance to drought and related abiotic stressors have been positively addressed via manipulation of IPT and/or CKX expression, much less attention has been paid to the CGTs. As naming of the CGTs has been unclear, we suggest COGT, CNGT, CONGT and CNOGT to describe the O‐, N‐ and dual function CGTs. As specific CGT mutants of both rice and arabidopsis showed impacts on yield components, we interrogated the wheat genome database, IWGSC RefSeq v1.0 & v2.0, to investigate wheat CGTs. Besides providing unambiguous names for the 53 wheat CGTs, we show their expression patterns in 70 developmental tissues and their response characteristics to various stress conditions by reviewing more than 1000 RNA‐seq data sets. These revealed various patterns of responses and showed expression generally being more limited in reproductive tissues than in vegetative tissues. Multiple cis‐regulatory elements are present in the 3 kb upstream of the start codons of the 53 CGTs. Elements associated with abscisic acid, light and methyl jasmonate are particularly over‐represented, indicative of the responsiveness of CGTs to the environment. These data sets indicate that CGTs have potential value for wheat improvement and that these could be targeted in TILLING or gene editing wheat breeding programmes.
Roles and regulation of cytokinins in tomato fruit development
Cytokinins (CKs) are thought to play important roles in fruit development, especially cell division. However, the mechanisms and regulation of CK activity have not been well investigated. This study analysed CK concentrations and expression of genes involved in CK metabolism in developing tomato (Solanum lycopersicum) ovaries. The concentrations of CK ribosides and isopentenyladenine and the transcript levels of the CK biosynthetic genes SlIPT3, SlIPT4, SlLOG6, and SlLOG8 were high at anthesis and decreased immediately afterward. In contrast, trans-zeatin concentration and the transcript levels of the CK biosynthetic genes SlIPT1, SlIPT2, SlCYP735A1, SlCYP735A2, and SlLOG2 increased after anthesis. The expression of type-A response regulator genes was high in tomato ovaries from pre-anthesis to early post-anthesis stages. These results suggest that the CK signal transduction pathway is active in the cell division phase of fruit development. This study also investigated the effect of CK application on fruit set and development. Application of a synthetic CK, N-(2-chloro-pyridin-4-yl)-N’-phenylurea (CPPU), to unpollinated tomato ovaries induced parthenocarpic fruit development. The CPPU-induced parthenocarpic fruits were smaller than pollinated fruits, because of reduction of pericarp cell size rather than reduced cell number. Thus, CPPU-induced parthenocarpy was attributable to the promotion of cell division, not cell expansion. Overall, the results provide evidence that CKs are involved in cell division during development of tomato fruit.
Strigolactone promotes cytokinin degradation through transcriptional activation of CYTOKININ OXIDASE/DEHYDROGENASE 9 in rice
Strigolactones (SLs), a group of terpenoid lactones derived from carotenoids, are plant hormones that control numerous aspects of plant development. Although the framework of SL signaling that the repressor DWARF 53 (D53) could be SL-dependently degraded via the SL receptor D14 and F-box protein D3 has been established, the downstream response genes to SLs remain to be elucidated. Here we show that the cytokinin (CK) content is dramatically increased in shoot bases of the rice SL signaling mutant d53. By examining transcript levels of all the CK metabolism-related genes after treatment with SL analog GR24, we identified CYTOKININ OXIDASE/DEHYDROGENASE 9 (OsCKX9) as a primary response gene significantly up-regulated within 1 h of treatment in the wild type but not in d53. We also found that OsCKX9 functions as a cytosolic and nuclear dual-localized CK catabolic enzyme, and that the overexpression of OsCKX9 suppresses the browning of d53 calli. Both the CRISPR/Cas9-generated OsCKX9 mutants and OsCKX9-overexpressing transgenic plants showed significant increases in tiller number and decreases in plant height and panicle size, suggesting that the homeostasis of OsCKX9 plays a critical role in regulating rice shoot architecture. Moreover, we identified the CK-inducible rice type-A response regulator OsRR5 as the secondary SL-responsive gene, whose expression is significantly repressed after 4 h of GR24 treatment in the wild type but not in osckx9. These findings reveal a comprehensive plant hormone cross-talk in which SL can induce the expression of OsCKX9 to down-regulate CK content, which in turn triggers the response of downstream genes.
Control of cytokinin and auxin homeostasis in cyanobacteria and algae
The metabolism of cytokinins (CKs) and auxins in vascular plants is relatively well understood, but data concerning their metabolic pathways in non-vascular plants are still rather rare. With the aim of filling this gap, 20 representatives of taxonomically major lineages of cyanobacteria and algae from Cyanophyceae, Xanthophyceae, Eustigmatophyceae, Porphyridiophyceae, Chlorophyceae, Ulvophyceae, Trebouxiophyceae, Zygnematophyceae and Klebsormidiophyceae were analysed for endogenous profiles of CKs and auxins and some of them were used for studies of the metabolic fate of exogenously applied radiolabelled CK, [ H]trans-zeatin (transZ) and auxin ([ H]indole-3-acetic acid (IAA)), and the dynamics of endogenous CK and auxin pools during algal growth and cell division. Quantification of phytohormone levels was performed by high-performance or ultrahigh-performance liquid chromatography-electrospray tandem mass spectrometry (HPLC-MS/MS, UHPLC-MS/MS). The dynamics of exogenously applied [ H]transZ and [ H]IAA in cell cultures were monitored by HPLC with on-line radioactivity detection. The comprehensive screen of selected cyanobacteria and algae for endogenous CKs revealed a predominance of bioactive and phosphate CK forms while O- and N-glucosides evidently did not contribute greatly to the total CK pool. The abundance of cis-zeatin-type CKs and occurrence of CK 2-methylthio derivatives pointed to the tRNA pathway as a substantial source of CKs. The importance of the tRNA biosynthetic pathway was proved by the detection of tRNA-bound CKs during the course of Scenedesmus obliquus growth. Among auxins, free IAA and its oxidation catabolite 2-oxindole-3-acetic acid represented the prevailing endogenous forms. After treatment with [ H]IAA, IAA-aspartate and indole-3-acetyl-1-glucosyl ester were detected as major auxin metabolites. Moreover, different dynamics of endogenous CKs and auxin profiles during S. obliquus culture clearly demonstrated diverse roles of both phytohormones in algal growth and cell division. Our data suggest the existence and functioning of a complex network of metabolic pathways and activity control of CKs and auxins in cyanobacteria and algae that apparently differ from those in vascular plants.