Prelunularic acid in liverworts

Prelunularic acid, the first example of an intermediate with a ‘pre-aromatic’ structure in the phenylpropanoid-polymalonate pathway, was isolated from suspension-cultured cells of Marchantia polymorpha. Its structure, including its absolute configuration, was assigned on the basis of spectral properties, direct conversion into lunularic acid, and CD measurements on the bis(p-dimethylaminobenzoate) of the methyl ester. Prelunularic acid was also detected in several liverworts of Marchantiales and Jungermanniales, and appears to be the immediate precursor of lunularic acid instead of the previously postulated hydrangenol or hydrangeic acid.     

Lunularic acid decarboxylase from the liverwort Conocephalum conicum

Some properties of a preparation of an enzyme, lunularic acid decarboxylase, from the liverwort Conocephalum conicum are described. The enzyme is normally bound and could be solubilized with Triton X-100; at least some of the bound decarboxylase activity appears to be associated with chloroplasts. For lunularic acid the enzyme has K_m 8.7 × 10^?5 M (pH 7.8 and 30°). Some substrate analogues have been tested but no other substrate was found. Pinosylvic acid is a competitive inhibitor for the enzyme, K_i 1.2 × 10^?4 M (pH 7.8 and 30°). No product inhibition was observed. Lunularic acid decarboxylase activity has also been observed with a cell-free system from Lunularia cruciata.     

GROWTH-INHIBITORS AND GROWTH-PROMOTERS IN ENTEROMORPHA COMPRESS A (CHLOROPHYTA)1

Methanol extracts from the alga Enteromorpha compressa (L.) Grev. contain substances which inhibit the elongation of Lepidium roots. Chromatographic separation of the inhibiting substances revealed that one of the inhibitory zones of the chromatograms had properties of the so-called inhibitor β. Neither abscisic acid (ABA) nor lunularic acid proved to be responsible for the growth-inhibiting property of this zone. Moreover, the extracts contain substances which promote the elongation of Avena coleoptile segments. One of these substances could be tentatively identified as indole-3-acetic acid by thin-layer and gas-liquid chromatography. (In addition to indole-3-acetic acid a second growth-promoting factor with the properties of the so-called accelerator α could be detected.)     

Growth and Dormancy in Lunularia cruciata (L.) Dum: VII. THE ISOLATION AND BIOASSAY OF LUNULARIC ACID

The extraction, purification, and isolation of the growth inhibitorpreviously postulated are described. Methanol extraction andseparation into acid, neutral, and basic fractions was followedby paper chromatography of the acid and neutral fractions withdistilled water, re-extraction with methanol, and thin-layerchromatography, the peak of inhibition being located at Rf 0.7–0.8(isopropanol: ammonia: water, 100:5:5), or Rf 0.3–0.4(chloroform: ethyl acetate: acetic acid, 60:40:5) Lunularia gemmae, grown directly on the chromatographic stripwith added nutrient solution, served as the most appropriateand direct bioassay. Area measurements after 5–10 days'growth yielded significant differences. Other bioassays included:Marchantia polymorpha gemmae, lettuce hypocotyl growth, cress-seedgermination, oat coleoptile, and radish cotyledon disc tests.An active inhibitor, i.e. dihydrohydrangeic acid, now named‘lunularic acid’, was isolated in crystalline form.Lunularic acid was found to increase with long-day treatmentof Lunularia thalli, though present even in short-day. Its concentrationcould be altered rapidly when daylength conditions were changed.The growth inhibition was linearly related to concentrationover the range from 0.1 to 10 ppm, very high concentrationsbeing lethal. Abscisic acid, though inhibitory to Lunulariain low concentrations, was not detected in extracts, and couldeasily be separated from lunularic acid.     

Effect of lunularic acid analogues on liverwort growth and IAA oxidation

The growth inhibitory activity of lunularic acid and a number of analogues has been examined in liverwort gemmaling and cress root growth tests. Lunularic acid was no more active than a wide range of similar compounds and no clear correlation between structure and activity was observed. The effects of these compounds, and of liverwort extracts, on in vitro IAA-oxidase activity was also examined.     

Ecology of epiphyllous liverworts: growth in three natural habitats in Western Nigeria

Abstract

The growth of four epiphyllous liverworts, Radula jiaccida, Caudalejeunea hanningtonii, Leptolejeunea astroidea, and Cololejeunea pusilla var. obtusifolia, has been followed for a period of about 18 months at three different localities in Western Nigeria over three height-ranges above the ground. The three localities experience different climatic conditions and possess different vegetation. Growth was found to be related to the size of the species, the larger ones always exhibiting faster growth. The liverworts also showed periodicity in growth, related to the wet and dry seasons. There was no period of dormancy, though growth was drastically reduced during the dry season.     

Intracellular Localization of Lunularic Acid and Prelunularic Acid in Suspension Cultured Cells of Marchantia polymorpha

Intracellular localization of lunularic acid and prelunularic acid in suspension cultured cells of Marchantia polymorpha L. was studied. The sum of both compounds was determined as lunularic acid group (LNAs) because of the instability of prelunularic acid to convert into lunularic acid.

Mechanical disruption of the cells followed by differential centrifugation showed that LNAs was associated with the supernatant of 100,000g centrifugation. Protoplasts isolated from the cells were osmotically ruptured and the distribution of LNAs among the organelles was examined by discontinuous density gradient centrifugation of the protoplast contents. Successful isolation of intact chloroplasts, mitochondria and peroxisomes free from cytoplasm indicated that LNAs was not accumulated in these organelles. Flotation techniques resulted in an efficient isolation of pure vacuoles and revealed that LNAs was distributed almost equally in the vacuoles and cytoplasm.

     

The detection and estimation of the growth inhibitor xanthoxin in plants

Summary The plant growth inhibitor xanthoxin which can be prepared in vitro by the oxidation of certain xanthophylls has been identified in the ether extracts of the shoots of a wide variety of higher plants. Gas liquid chromatography of an acetylated derivative has been used for its quantitative estimation.Evidence is provided that xanthoxin is a true endogenous inhibitor and that violaxanthin or a related xanthophyll epoxide is its biogenetic precursor. The importance of xanthoxin and its relationship with abscisic acid and other plant growth inhibitors is discussed.     

The mode of action of thidiazuron: auxins,indoleamines, and ion channels in the regeneration of <Emphasis Type="Italic">Echinacea purpurea</Emphasis> L.

The biochemical mechanisms underlying thidiazuron (TDZ)-induced regeneration in plant cells have not been clearly elucidated. Exposure of leaf explants of Echinacea purpurea to a medium containing TDZ results in undifferentiated cell proliferation and differentiated growth as mixed shoot organogenesis and somatic embryogenesis. The current studies were undertaken to determine the potential roles of auxin, indoleamines, and ion signaling in the dedifferentiation and redifferentiation of plant cells. E. purpurea leaf explants were found to contain auxin and the related indoleamine neurotransmitters, melatonin, and serotonin. The levels of these endogenous indoleamines were increased by exposure to TDZ associated with the induction of regeneration. The auxin-transport inhibitor 2,3,5-triiodobenzoic acid and auxin action inhibitor, p-chlorophenoxyisobutyric acid decreased the TDZ-induced regeneration but increased concentrations of endogenous serotonin and melatonin. As well, inhibitors of calcium and sodium transport significantly reduced TDZ-induced morphogenesis while increasing endogenous indoleamine content. These data indicate that TDZ-induced regeneration is the manifestation of a metabolic cascade that includes an initial signaling event, accumulation, and transport of endogenous plant signals such as auxin and melatonin, a system of secondary messengers, and a concurrent stress response.     

The concentrations of lunularic acid and prelunularic acid in liverworts

The amounts of lunularic acid in suspension cultured cells of Marchantia polymorpha and thallus of Conocephalum conicum were carefully re-exami     

Metabolism of lunularic acid in liverworts

The presence, in Conocephalum conicum, of the enzymes phenylalanine ammonia lyase, trans-cinnamic acid-4-hydroxylase and lunularic acid decarbo     

Exploring the plastid genome disparity of liverworts

Sequencing the plastid genomes of land plants provides crucial improvements to our understanding of the plastome evolution of land plants. Although the number of available complete plastid genome sequences has rapidly increased in the recent years, only a few sequences have been yet released for the three bryophyte lineages, namely hornworts, liverworts, and mosses. Here, we explore the disparity of the plastome structure of liverworts by increasing the number of sequenced liverwort plastomes from five to 18. The expanded sampling included representatives of all major lineages of liverworts including the genus Haplomitrium. The disparity of the liverwort genomes was compared with other 2386 land plant plastomes with emphasis on genome size and GC‐content. We found evidence for structural conservatism of the plastid genomes in liverworts and a trend towards reduced plastome sequence length in liverworts and derived mosses compared to other land plants, including hornworts and basal lineages of mosses. Furthermore, Aneura and Haplomitrium were distinct from other liverworts by an increased GC content, with the one found in Haplomitrium only second to the lycophyte Selaginella. The results suggest the hypothesis that liverworts and other land plants inherited and conserved the plastome structure of their most recent algal ancestors.     

Breaking of Dormancy in Xanthium Seeds by Kinetin Mediated by Light and DNA-dependent RNA Synthesis

Kinetin was able to break the dormancy of the “upper seed” (in bur) of Xanthium by antagonizing the endogenous inhibitor present in the embryo. Other growth substances like indoleacetic acid, gibberellic acid and cycocel were without effect. Breaking of dormancy by kinetin was dependent on reversible phytochrome system and DNA-dependent RNA synthesis. Protein synthesis is possibly not involved in the act of dormancy breaking. Endogenous inhibitor possibly participates in the mechanism of repression of genie site(s). It is suggested that an interplay of endogenous inhibitors, kinins and other factors (light, temperature, etc.) regulate dormancy, germination and differentiation by repression and derepression of DNA sites.     

广西中越边境喀斯特地区叶附生苔类植物物种多样性研究

为了解日益恶化的喀斯特环境下叶附生苔类植物的分布状况,对广西中越边境喀斯特地区叶附生苔类植物多样性展开调查。结果表明,广西中越边境喀斯特地区有叶附生苔类植物5科15属43种,其中,九洲疣鳞苔(Cololejeunea yakusimensis)、巴氏薄鳞苔(Leptolejeunea balansae)、斯氏唇鳞苔(Cheilolejeunea streimannii)、麦氏细鳞苔(Lejeunea micholitzii)、巨齿细鳞苔(L.kodamae)和纤细细鳞苔(L.exilis)为广西苔藓植物新记录。该地区叶附生苔类植物区系具有热带性质和东亚分布特点。与邻近地区比较,该地区叶附生苔类植物与贵州茂兰的亲缘关系和区系关系最紧密。该地区叶附生苔类植物分布随海拔增加呈增加趋势。那坡老虎跳保护区、龙州和宁明弄岗保护区以及靖西龙邦镇风水林是叶附生苔类植物分布最丰富的地区,因此,建议应对这些地区的叶附生苔类植物进行优先保护。     

Phytohormone Profiling across the Bryophytes

BackgroundBryophytes represent a very diverse group of non-vascular plants such as mosses, liverworts and hornworts and the oldest extant lineage of land plants. Determination of endogenous phytohormone profiles in bryophytes can provide substantial information about early land plant evolution. In this study, we screened thirty bryophyte species including six liverworts and twenty-four mosses for their phytohormone profiles in order to relate the hormonome with phylogeny in the plant kingdom.MethodologySamples belonging to nine orders (Pelliales, Jungermanniales, Porellales, Sphagnales, Tetraphidales, Polytrichales, Dicranales, Bryales, Hypnales) were collected in Central and Northern Bohemia. The phytohormone content was analysed with a high performance liquid chromatography electrospray tandem-mass spectrometry (HPLC-ESI-MS/MS).ConclusionThe apparent differences in conjugation and/or degradation strategies of growth hormones between liverworts and mosses might potentially show a hidden link between vascular plants and liverworts. On the other hand, the complement of stress hormones in bryophytes probably correlate rather with prevailing environmental conditions and plant survival strategy than with plant evolution.     

Physiological Roles of Brassinosteroids in Early Growth of <Emphasis Type="Italic">Arabidopsis:</Emphasis> Brassinosteroids Have a Synergistic Relationship with Gibberellin as well as Auxin in Light-Grown Hypocotyl Elongation

We examined the physiological effects of brassinosteroids (BRs) on early growth of Arabidopsis. Brassinazole (Brz), a BR biosynthesis inhibitor, was used to elucidate the significance of endogenous BRs. It inhibited growth of roots, hypocotyls, and cotyledonous leaf blades dose-dependently and independent of light conditions. This fact suggests that endogenous BRs are necessary for normal growth of individual organs of Arabidopsis in both photomorphogenetic and skotomorphogenetic programs. Exogenous brassinolide (BL) promoted hypocotyl elongation remarkably in light-grown seedlings. Cytological observation disclosed that BL-induced hypocotyl elongation was achieved through cell enlargement rather than cell division. Furthermore, a serial experiment with hormone inhibitors showed that BL induced hypocotyl elongation not through gibberellin and auxin actions. However, a synergistic relationship of BL with gibberellin A₃ (GA₃) and indole-3-acetic acid (IAA) was observed on elongation growth in light-grown hypocotyls, even though gibberellins have been reported to be additive to BR action in other plants. Taken together, our results show that BRs play an important role in the juvenile growth of Arabidopsis; moreover, BRs act on light-grown hypocotyl elongation independent of, but cooperatively with, gibberellins and auxin.     

Plant Mitochondrial RNA Editing

RNA editing affects messenger RNAs and transfer RNAs in plant mitochondria by site-specific exchange of cytidine and uridine bases in both seed and nonseed plants. Distribution of the phenomenon among bryophytes has been unclear since RNA editing has been detected in some but not all liverworts and mosses. A more detailed understanding of RNA editing in plants required extended data sets for taxa and sequences investigated. Toward this aim an internal region of the mitochondrial nad5 gene (1104 nt) was analyzed in a large collection of bryophytes and green algae (Charales). The genomic nad5 sequences predict editing in 30 mosses, 2 hornworts, and 7 simple thalloid and leafy liverworts (Jungermanniidae). No editing is, however, required in seven species of the complex thalloid liverworts (Marchantiidae) and the algae. RNA editing among the Jungermanniidae, on the other hand, reaches frequencies of up to 6% of codons being modified. Predictability of RNA editing from the genomic sequences was confirmed by cDNA analysis in the mosses Schistostega pennata and Rhodobryum roseum, the hornworts Anthoceros husnotii and A. punctatus, and the liverworts Metzgeria conjugata and Moerckia flotoviana. All C-to-U nucleotide exchanges predicted to reestablish conserved codons were confirmed. Editing in the hornworts includes the removal of genomic stop codons by frequent reverse U-to-C edits. Expectedly, no RNA editing events were identified by cDNA analysis in the marchantiid liverworts Ricciocarpos natans, Corsinia coriandra, and Lunularia cruciata. The findings are discussed in relation to models on the phylogeny of land plants. Received: 2 April 1998 / Accepted: 4 August 1998     

Lunularic acid and related compounds in liverworts,algae and Hydrangea

Lunularic acid and lunularin were detected in 76 species of hepatics, but not in any of the Anthrocerotales or Algae examined. Lunularic acid, lunularin, 3,4′-dihydroxystilbene and a glycoside of lunularic acid were also identified in extracts of Hydrangea macrophylla roots, together with hydrangenol, hydrangeic acid and their glucosides.     

Phosphatidylinositol‐specific phospholipase C2 functions in auxin‐modulated root development

Nine phosphatidylinositol‐specific phospholipases C (PLCs) have been identified in the Arabidopsis genome; among the importance of PLC2 in reproductive development is significant. However, the role of PLC2 in vegetative development such as in root growth is elusive. Here, we report that plc2 mutants displayed multiple auxin‐defective phenotypes in root development, including short primary root, impaired root gravitropism, and inhibited root hair growth. The DR5:GUS expression and the endogenous indole‐3‐acetic acid (IAA) content, as well as the responses of a set of auxin‐related genes to exogenous IAA treatment, were all decreased in plc2 seedlings, suggesting the influence of PLC2 on auxin accumulation and signalling. The root elongation of plc2 mutants was less sensitive to the high concentration of exogenous auxins, and the application of 1‐naphthaleneacetic acid or the auxin transport inhibitor N‐1‐naphthylphthalamic acid could rescue the root hair growth of plc2 mutants. In addition, the PIN2 polarity and cycling in plc2 root epidermis cells were altered. These results demonstrate a critical role of PLC2 in auxin‐mediated root development in Arabidopsis, in which PLC2 influences the polar distribution of PIN2.