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Cell cycle regulation by plant growth regulators: involvement of auxin and cytokinin in the re-entry of Petunia protoplasts into the cell cycle.

In order to understand the mode of action of auxins and cytokinins in the induction of cell division, the effects of the two plant growth regulators 2,4-dichlorophenoxyacetic acid (2,4-D) and N6-benzyladenine (BA) were investigated using mesophyll protoplasts of Petunia hybrida, cultivated in either complete medium or in medium deficient in cytokinin, auxin or both. Firstly we studied DNA synthesis, using 5-bromodeoxyuridine/bisbenzimide Hoechst/propidium iodide flow cytometry analyses and by the monitoring of histone H4 transcript levels. Roscovitine, a cyclin-dependent kinase (CDK) inhibitor, was found to block the cell cycle prior to entry into the S and M phases in the cultured P. hybrida protoplasts. This suggests that in Petunia cell there is a requirement for CDK activity in order to complete the G1 and G2 phases. Further experiments using roscovitine showed that neither 2,4-D nor BA were individually able to induce cell cycle progression beyond the roscovitine G1 arrest. We also monitored the phytohormonal induction of S phase by studying variations in transcript levels of the gene for mitogenactivated protein kinase (PMEK1) and transcript levels of the cell division cycle gene cdc2Pet. Only 2,4-D, and not BA, was able to stimulate PMEK1 gene transcription; thus, the more rapid S-phase induction in 2,4-D-treated protoplasts may be attributable to the activation of this transduction pathway. In contrast, both plant growth regulators were required to induce the appearance of cdc2Pet mRNA transcripts prior to S-phase engagement.

2,4-Dichlorophenoxyacetic Acid↗

On the structure of calonyctin A, a plant growth regulator.

The plant growth regulator calonyctin A, isolated from the dried leaves of Calonyction aculeatum L. House (Yue-Guang-Hua), was separated into two pure components by high performance liquid chromatography. By use of mass spectrometry based on various ionization techniques, one- and two-dimensional NMR spectroscopy, IR spectrometry, and chemical methods the molecular structures of the two homologous glycosides were determined. Each molecule contains two hydroxy fatty acid residues and four 6-deoxyhexose units. The fatty acids are 3-hydroxy-2-methylbutanoic acid and 11-hydroxytetradecanoic acid or 11-hydroxyhexadecanoic acid. The 6-deoxyhexose residues (three of quinovose and one of rhamnose) comprise a tetrasaccharide having the following structure: [formula: see text] The long-chain hydroxy acid is linked glycosidically through its O-11 to Qui D and esterified to O-2 of Qui C, forming a macrocyclic lactone. The 3-hydroxy-2-methylbutanoic acid is ester-linked to O-3 of Qui C.

Carbohydrate Conformation↗

Regulatory and functional interactions of plant growth regulators and plant glutathione S-transferases (GSTs).

Plant glutathioneS-transferases (GSTs) are a heterogeneous superfamily of multifunctional proteins, grouped into six classes. The tau (GSTU) and phi (GSTF) class GSTs are the most represented ones and are plant-specific, whereas the smaller theta (GSTT) and zeta (GSTZ) classes are also found in animals. The lambda GSTs (GSTL) and the dehydroascorbate reductases (DHARs) are more distantly related. Plant GSTs perform a variety of pivotal catalytic and non-enzymatic functions in normal plant development and plant stress responses, roles that are only emerging. Catalytic functions include glutathione (GSH)-conjugation in the metabolic detoxification of herbicides and natural products. GSTs can also catalyze GSH-dependent peroxidase reactions that scavenge toxic organic hydroperoxides and protect from oxidative damage. GSTs can furthermore catalyze GSH-dependent isomerizations in endogenous metabolism, exhibit GSH-dependent thioltransferase safeguarding protein function from oxidative damage and DHAR activity functioning in redox homeostasis. Plant GSTs can also function as ligandins or binding proteins for phytohormones (i.e., auxins and cytokinins) or anthocyanins, thereby facilitating their distribution and transport. Finally, GSTs are also indirectly involved in the regulation of apoptosis and possibly also in stress signaling. Plant GST genes exhibit a diversity of expression patterns during biotic and abiotic stresses. Stress-induced plant growth regulators (i.e., jasmonic acid [JA], salicylic acid [SA], ethylene [ETH], and nitric oxide [NO] differentially activate GST gene expression. It is becoming increasingly evident that unique combinations of multiple, often interactive signaling pathways from various phytohormones and reactive oxygen species or antioxidants render the distinct transcriptional activation patterns of individual GSTs during stress. Underestimated post-transcriptional regulations of individual GSTs are becoming increasingly evident and roles for phytohormones (i.e., ABA and JA) in these processes are being anticipated as well. Finally, indications are emerging that NO may regulate the activity of specific plant GSTs. In this review, the current knowledge on the regulatory and functional interactions of phytohormones and plant GSTs are covered. We refer to a previous extensive review on plant GSTs (Marrs, 1996) for most earlier work. An introduction on the classification and roles of plant GSTs is included here, but these topics are more extensively discussed in other reviews (Dixon et al., 2002a; Edwards et al., 2000; Frova, 2003).

Gene Expression↗

Screening of plant growth regulators acting on Arabidopsis thaliana.

Our screening system using Arabidopsis thaliana, enabled us to evaluate the effect of 38 known growth regulators on plant growth promotion. Eleven compounds in the study were found to show a promoting effect upon Arabidopsis dry weight and leaf number; in particular, oligosaccharides (OS) such as raffinose and stachyose had a marked effect. Detailed experiments indicated that the effect of OS on plant growth was not merely derived from its potential carbon source. Among the monosaccharides comprising stachyose, galactose showed the best promoting effect on plant growth.

Arabidopsis↗

A UV-light activated cinnamic acid isomer regulates plant growth and gravitropism via an ethylene receptor-independent pathway.

Naturally occurring cinnamic acids (CA) exist in both trans- and cis-isoforms. UV-light irradiation of trans-CA is able to produce cis-CA. cis-CA was found to possess auxin-like activity before. In contrast, the vapor of cis-CA induced an epinastic response in tomato plants just as ethylene does. Given the existence of a double bond in and the gaseous nature of cis-CA, we suspected that cis-CA might also function as an ethylene-like compound. To distinguish between these possibilities, we selected an ethylene perception-deficient tomato plant, Never-ripe (Nr), and an ethylene biosynthesis-deficient tomato plant, A11. Not only did the vapor of cis-CA fail to trigger A11 tomato fruit ripening but it also delayed the ripening of banana fruit. Moreover, the vapor of cis-CA induced epinasty and the 'triple response' in both the wild type and Nr tomato plants, indicating that the vapor of cis-CA does not act via an ethylene receptor-dependent pathway. Furthermore, the vapor of cis-CA inhibited the negative gravitropic response of stems of both etiolated Nr seedlings and young plants, whereas ethylene had little effect on the negative gravitropism of the Nr plants. These results support the conclusion that the action sites of the vapor of cis-CA and ethylene are fundamentally different.

Arabidopsis↗

On plant growth regulators and their metabolites: a changing perspective.

From seed germination to vegetative growth and flowering virtually all aspects of plant growth and development are influenced by structurally relatively simple substances, termed phytohormones. It has been argued that the wide range of responses elicited by these substances requires a mode of action that is radically different from those of animal hormones. In contrast to animal hormones, it is often very difficult to distinguish between the site of synthesis and the site of action of phytohormones. Hence, plants may have developed their own mechanisms for synthesis, sequestration and release of active hormones. Current evidence indicates that enzymes that can synthesize and modify phytohormones and their antagonists or hydrolyze phytohormone conjugates to release active hormones which play a role in initiating important regulatory pathways. They are also likely to provide invaluable tools for studying the mechanisms underlying growth and development in plants.

Bacteria↗

[Effects of light and plant growth regulators on growth of normal and hairy root of Lycium barbarum in vitro].

OBJECTIVE: To study effects of the cycle of light and exogenous plant growth regulators on growth of normal root and hairy root of Lycium barbarum and establish a long-term system of in vitro culture of L. barbarum roots. METHOD: Using normal roots from aseptic seedlings and hairy roots originated from Agrobacterium rhizogenes A4-mediated genetic transformation of L. barbarum, the growth of root segments was examined after 20 days of culture under different culture conditions. RESULT AND CONCLUSION: When cultured on the MS medium with different plant growth regulators (IAA, IBA, NAA), normal root segments of L. barbarum could elongate and branch, and the addition of 1 mg x L(-1) IBA into the medium was the most suitable for long-term in vitro culture of L. barbarum root. When cultured on MS medium without hormone, light promoted the elongation and lateral root formation of type II hairy root, but not of type I hairy root. Among three tested hormones, IAA at low concentration was the best for growth of type I hairy root, while 1 mg x L(-1) IBA was the most suitable for growth of type II hairy root. With the increase of hormone level added into MS medium, callusing frequencies of type I, II hairy roots were increased, at the same time, the formation of lateral root from hairy root or callus was inhibited.

Culture Media↗

Achieving desired plant growth regulator levels in liquid plant tissue culture media that include activated carbon.

This paper is part of a series considering the impact of activated carbon (AC) on the composition of plant tissue culture media. Using liquid culture media for initiation of Norway spruce embryogenic tissue and eight different ACs, we present a method for achieving target plant growth regulator (PGR) levels in AC-containing medium based on sorption isotherms for individual PGRs. Linear relationships were found between PGR adsorption and specific BET (Brunauer, Emmett, Teller theory) surface area and specific total pore volume of AC. When using a new AC, this linear relationship allows one to achieve multiple PGR levels similar to historic levels through adjustment of the mass of AC based on its relative BET surface area or relative total pore volume. Target levels of PGRs and an initiation success similar to that in medium without AC were achieved with several different AC types when AC mass was adjusted on the basis of pore volume.

Cell Culture Techniques↗

Effects of the plant growth regulator, chlormequat, on mammalian fertility.

This paper summarizes the consequences of exposure to chlormequat, a plant growth regulator, on reproduction in mammals. Plant growth regulators are chemicals used to manipulate plant growth, flowering and fruit yield. In grain crops, plant growth regulators are applied to promote sturdier growth and reduce the risk of lodging. Chlormequat is the most common plant growth regulator. Maximum residue limits of chlormequat in food products are 10 mg/kg in oat and pear, 3 mg/kg in wheat and rye, and 0.5 mg/kg in milk. In Denmark, results from experiments with pigs in the late 1980s showed sows that display impaired reproduction, mainly impaired oestrus, when fed grain from crop treated with chlormequat. Subsequently, the advisory body to the Danish pig industry recommended limiting the use of grain (maximum 30% of diet energy) from crop treated with chlormequat given to breeding stock due to the risk of reproduction problems. More recently, experiments have been conducted to evaluate the influence of chlormequat-treated wheat crop on reproductive function in male and female mice. These experiments showed that epididymal spermatozoa from mice on feed or water containing chlormequat had compromised fertilizing competence in vitro, while reproduction in female mice was not compromised. The estimated intake of chlormequat in the pig (0.0023 mg/kg bw/day) and the mouse (0.024 mg/kg bw/day) experiments was below the acceptable daily intake of 0.05 mg/kg bw/day. Reports from the industry do not show any effects at these low levels.

Animals↗

Myxostiolide, myxostiol, and clavatoic acid, plant growth regulators from the fungus Myxotrichum stipitatum.

New plant growth regulators, named myxostiolide (1), myxostiol (2), and clavatoic acid (3), have been isolated from Myxotrichum stipitatum, and their structures have been established by spectroscopic methods including 2D NMR. The biological activities of 1, 2, and 3 have been examined using tea pollen and lettuce seedling bioassay methods. With tea pollen, compound 1 inhibited the pollen tube growth to 14% of control at a concentration of 100 mg/L. With lettuce seedlings, compound 2 accelerated the root growth from 1 mg/L to 100 mg/L and compound 3 inhibited the root growth, to 52% of control, at a concentration of 100 mg/L.

Benzoates↗

[Effect of several plant growth regulators on various prokaryotes and their viruses].

26 plant growth regulators including herbicides were investigated in their effect on the multiplication of Escherichia coli, Bacillus subtilis, and the blue-green alga Plectonema boryanum as well as the RNA phages M 12 and Qbeta and the DNA phages lambda, phi 105, and LPP-1 employing the agar diffusion method. Nearly all of the compounds inhibited and/or stimulated one or some of the prokaryotes tested. The most frequent and strongest effects occurred in Pl. boryanum, the least effects in E. coli. The multiplication of phages was also influenced by plant growth regulators leading to increase, decrease or non-appearance of plaques. The investigations with the temperate phages lambda and phi 105 suggested part of the compounds to be able to interfere with the process of lysogenization. The results are discussed comparatively involving correspondent findings referred to in literature.

Bacillus subtilis↗

[Separation and determination of plant growth regulators by capillary micellar electrokinetic chromatography].

It is important for separation and determination of plant growth regulators in the research of plant physiology. A study of the separation of five plant growth regulators, such as abscisic acid (ABA), gibberellic acid (GA), indole-butyric acid (IBA), indole acetic acid (IAA) and naphthaleneacetic (NAA) by micellar electrokinetic chromatography (MEKC) is presented. The effects of pH, SDS concentration, applied voltage and organic additives on migration behavior were investigated. Results showed that satisfactory separation was achieved on optimization of electrophoretic condition: 80 mmol/L SDS, 10 mmol/L borate-phosphate, 5% isopropanol, 18 kV applied voltage, pH 8.0. The SDS concentration and organic additives played an important role in separating plant growth regulators, and the applied voltage and pH gave less effect. The detection limit of ABA, GA, IBA, IAA and NAA were 5.0 x 10(-3), 3.0 x 10(-3), 5.8 x 10(-4), 1.5 x 10(-4) and 1.4 x 10(-4) g/L respectively. Increasing of the SDS concentration or organic additives would change separation factor (alpha) and result an improvement of the resolution of difficult separation pairs ABA-GA and IAA-NAA.

Abscisic Acid↗

Quantitative expression analysis of GH3, a gene induced by plant growth regulator herbicides in soybean.

Symptoms resembling off-target plant growth regulator (PGR) herbicide injury are frequently found in soybean fields, but the causal agent is often difficult to identify. The expression of GH3, an auxin-regulated soybean gene, was quantified from soybean leaves injured by PGR herbicides using real-time RT-PCR. Expression of GH3 was analyzed to ascertain its suitability for use in a diagnostic assay to determine whether PGR herbicides are the cause of injury. GH3 was highly induced by dicamba within 3 days after treatment (DAT) and remained high at 7 DAT, but induction was much lower at 17 DAT. GH3 was also highly induced at 7 DAT by dicamba + diflufenzopyr, and to a lesser extent by the other PGR herbicides clopyralid and 2,4-D. The non-PGR herbicides glyphosate, imazethapyr, and fomesafen did not significantly induce GH3 expression above a low constitutive level. These results indicate that a diagnostic assay for PGR herbicide injury based on overexpression of auxin-responsive genes is feasible, and that GH3 is a potential candidate from which a diagnostic assay could be developed. However, time course analysis of GH3 expression indicates the assay would be effective for a limited time after exposure to the herbicide.

Gene Expression↗