Microbial Resolution of (±)-Borneols

(±)-Bornyl acetate and (±)-isobornyl acetate were asymmetrically hydrolyzed by microorganisms to give (?)-borneol with (+)-bornyl acetate and (?)-isoborneol with (+)-isobornyl acetate although in low hydrolytic ratios. On the contrary (±)-bornyl chloroacetate and (±)-isobornyl chloroacetate were easily hydrolyzed by microorganisms to afford (?)-borneol and (?)-isoborneol with the acetate of their antipodes. Also, enzymatic hydrolysis of (±)-menthyl chloroacetate proceeded faster than that of (±)-menthyl acetate.     

Highly selective biotransformation of (+)-(1S)- and (−)-(1R)-camphorquinone by Aspergillus wentii

Abstract

To clarify the structures of biotransformation products and metabolic pathways, the biotransformation of monoterpenoids, (+)- and (?)-camphorquinone (1a and b), has been investigated using Aspergillus wentii as a biocatalyst. Compound 1a was converted to (?)-(2S)-exo-hydroxycamphor (2a), (?)-(2S)-endo-hydroxycamphor (3a), (?)-(3S)-exo-hydroxycamphor (4a), (?)-(3S)-endo-hydroxycamphor (5a), and (+)-camphoric acid (6a). Compound 1b was converted to (+)-(2R)-exo-hydroxycamphor (2b), (+)-(2R)-endo-hydroxycamphor (3b), (+)-(3R)-exo-hydroxycamphor (4b), (+)-(3R)-endo-hydroxycamphor (5b), and (?)-camphoric acid (6b). Compound 1a mainly produced 2a (65.0%) with stereoselectivity, whereas 1b afforded 3b (84.3%) with high stereoselectivity. These structures were confirmed by gas chromatography–mass spectrometry, infrared, ¹H nuclear magnetic resonance (NMR), and ¹³C NMR spectral data. The products illustrate the marked ability of A. wentii for enzymatic oxidation and ketone reduction.     

Chirality of terpenoids isolated from the liverwort Conocephalum conicum

Reinvestigation of a Japanese sample of the thalloid liverwort Conocephalum conicum afforded (+)-bornyl ferulate and bornyl 2 - methoxy - 4 - hydroxycinnamate together with (?) - limonene, (?) - β - sabinene, (+) - bicycloelemene, (+) - β - elemene, (?) - bicyclogermacrene, lunularin, and the two compounds, 1 - octen - 3 - ol and 1 - octen - 3 - yl acetate, responsible for the mushroom-like odour of the crushed thallus. The chirality of the compounds isolated is discussed.     

Two flavonoids from tephrosia purpurea

Purpurenone, a new β-hydroxychalcone; (+)-purpurin, a diastereoisomer of(?)purpurin; dehydroisoderricin, and (?)-maackiain have been isolated from the roots of Tephrosio purpurea in addition to the earlier reported flavonoids [1, 2]. Pseudosemiglabrin was obtained in admixture with (?)-semiglabrin     

Is it possible to manipulate root anchorage in young trees?

The optimal root system architecture for increased tree anchorage has not yet been determined and in particular, the role of the tap root remains elusive. In Maritime pine (Pinus pinaster Ait.), tap roots may play an important role in anchoring young trees, but in adult trees, their growth is often impeded by the presence of a hard pan layer in the soil and the tap root becomes a minor component of tree anchorage. To understand better the role of the tap root in young trees, we grew cuttings (no tap root present) and seedlings where the tap root had (?) or had not (+) been pruned, in the field for 7 years. The force (F) necessary to deflect the stem sideways was then measured and divided by stem cross-sectional area (CSA), giving a parameter analogous to stress during bending. Root systems were extracted and root architecture and wood mechanical properties (density and longitudinal modulus of elasticity, E _L ) determined. In seedlings (?) tap roots, new roots had regenerated where the tap root had been pruned, whereas in cuttings, one or two lateral roots had grown downwards and acted as tap roots. Cuttings had significantly less lateral roots than the other treatments, but those near the soil surface were 14% and 23% thicker than plants (+) and (?) tap roots, respectively. Cuttings were smaller than seedlings, but were not relatively less resistant to stem deflection, probably because the thicker lateral roots compensated for their lower number. Apart from stem volume which was greater in trees (+) tap roots, no significant differences with regard to size or any root system variable were found in plants (?) or (+) tap roots. In all treatments, lateral roots were structurally reinforced through extra growth along the direction of the prevailing wind, which also improved tap root anchorage. Predictors of log F/CSA differed depending on treatment: in trees (?) tap roots, a combination of the predictors stem taper and %volume allocated to deep roots was highly regressed with log F/CSA (R ² = 0.83), unlike plants (+) tap roots where the combined predictors of lateral root number and root depth were best regressed with log F/CSA (R ² = 0.80). In cuttings, no clear relationships between log F/CSA and any parameter could be found. Wood density and E _L did not differ between roots, but did diminish with increasing distance from the stem in lateral roots. E _L was significantly lower in lateral roots from cuttings. Results showed that nursery techniques influence plant development but that the architectural pattern of Maritime pine root systems is stable, developing a sinker root system even when grown from cuttings. Anchorage is affected but the consequences for the long-term are still not known. Numerical modelling may be the only viable method to investigate the function that each root plays in adult tree anchorage.     

Alkaloids of Thermopsis Lupinoides

Ammodendrine, together with seven other known lupin alkaloids, was isolated from Thermopsis lupinoides. (+)-Lupanine (+)-17-oxolupanine occurred together with (?)anagyrine, (?)-baptifoline, (?)-cytisine, (?)-N-methylcytisine (?)N-formylcytisine. These alkaloids have the opposite stereochemistry to that of (+)-lupanine and (+)-17-oxolupanine. The distribution of alkaloids in fresh flowers, leaves, stems roots of this plant was also examined.     

Cell division activation in the quiescent center of excised maize root tip

The phenomenon of activating cell proliferation in the quiescent center of excised maize roots is described. The root tips were grown on wet filter paper in Petri dishes. This phenomenon was observed in 8 to 14 maize cultivars and was absent in excised Arabidopsis root tips. The distribution of mitoses in meristems greatly varied in individual seedlings roots from the same seed lot and seedlings of different cultivars. Meristem opening was observed after the removal of small root tips not longer than 3 mm and intact seminal roots. Sucrose (2%) and 10⁻⁶–10⁻⁸ M indole-3-acetic acid did not prevent meristem opening. These findings indicate that the state of quiescent center is maintained by a system of intercellular and interorgan relations, which are to be clarified.     

盐胁迫对二穗短柄草幼苗生长及不同器官中盐离子稳态的影响

采用4种浓度的NaCl溶液(50、100、150、200 mmol/L)处理二穗短柄草和拟南芥(对照)幼苗,测定不同浓度盐胁迫下2种植物幼苗的生长指标和离子分布,以探讨二穗短柄草在盐胁迫下主要阳离子平衡机制.结果表明:(1)盐胁迫显著抑制二穗短柄草根叶的生物量积累.(2)根冠比数据显示,在盐胁迫条件下二穗短柄草能够更好地维系地下部分的生物量积累.(3)在4种浓度盐胁迫下,二穗短柄草叶中Na+含量低于根系,而且K+、Cl-含量和K+/Na+比值始终高于根系,说明在二穗短柄草中Na+从地下到地上的转运受到抑制,但对Cl-的转运缺乏有效的调控.(4)回归分析发现,盐胁迫下二穗短柄草和拟南芥根部Na+与K+含量变化呈正相关关系,而在叶部则不相关,说明二穗短柄草和拟南芥Na+与K+在根部具有相同的离子通道,而在叶部却具有各自独立的转运途径.     

Preparation of Optically Pure cis-2,4-Dimethyl-l-cyclohexanones,the Key Intermediates in Cycloheximide Synthesis,Using Microbial Resolution

Asymmetric hydrolysis of acetate (10) of (±)-t-2,t-4-dimethyl-r-l-cyclohexanol with Bacillus subtilis var. niger gave (?)-(lS,2S,4S)-2,4-dimethyl-l-cyclohexanol (6a) and (+)-(1R,2R,4R)-acetate (10b) with high optical purities. Optically pure (?) and (+)-alcohols (6a and 6b) were prepared via corresponding 3,5-dinitrobenzoates. Oxidation of alcohols (6a and 6b) with chromic acid gave optically pure (?)-(2S,4S) and (+)-(2R,4R)-2,4-dimethyl-l-cyclohexanones (2a and 2b), respectively.     

Effect of the interaction between light and touch stimuli on inducing curling seminal roots in rice seedlings

Root development is sensitive to environmental stimuli. We have recently reported that the light signal could promote the helical growth of seminal roots and drive the wavy root morphology in rice (Oryza sativa L.) young seedlings. The light-stimulated wavy roots were mostly performed in indica-type rice varieties (e.g., Taichung Native 1; TCN1) but not in japonica rice (e.g., Tainung 67; TNG67). Here, we demonstrated that the light-driven circumutation trajectory of TCN1 seminal roots could be changed if the seedling roots were grown in the medium containing high concentration of Phytagel. The data showed the root morphology would be modulated from wavy to curling when the Phytagel concentration was increased to 2%. However, the touch-stimulated curling root phenotype could not be performed in dark. In addition, the touch-induced curling roots were not appeared in the TNG67 rice cultivar. Although touch stimuli could not induce wavy/curling root phenotype in dark, it could modify the light-promoted helical growth to conduct curling roots in TCN1 rice seedlings. Thus, it was suggested that there is a crosstalk mechanism between touching-induced root curling and light-stimulated root waving.Key words: curling root, light stimuli, Oryza sativa, seminal root, touch stimuli, wavy rootRoot development and architecture could be changed to adapt the environmental conditions. Although root is usually grown in soil, it still exposes to light penetrated through soil particles. Some studies also indicated light can be conducted from shoots to roots through vascular bundle tissues.^1,2 Recently, we have reported that the light-exposed seminal roots of indica-type rice, i.e., Taichung Native 1 (TCN1), presented the wavy morphology.³ The light-induced wavy root was not performed in japonica rice such as Tainung 67 (TNG67). Moreover, the circumutation of TCN1 seminal root tip were observed with time-lapse photography during root growth. According to the investigations among various rice varieties, it has been found that the root morphology was determined by helix period and circumnutation trajectory of root tip moving behavior.³ For example, the root tip movement of light-exposed TCN1 seedlings was a regular circumntation; therefore, the roots performed a regular wavy phenotype. In the other rice variety (i.e., Taichung Sen 17) with the curling root morphology, the circumnutation trajectory of seminal roots was significantly irregular compared with that was observed in TCN1. In the previous report, we showed that the auxin and oxylipins (i.e., ketol) played important roles to trigger the light-induced wavy roots.³The wavy root phenotype has also been observed in Arabidopsis when it was cultured on an agar-plate that was inclined at an angle of less than 90°.⁴ Based on the studies in Arabidopsis mutants, the performance of obstacle-touching induced wavy phenotype in seedlings roots was related to the functions of auxin efflux/influx carriers and some proteins involved in cell expansion.^4–6 Moreover, ethylene also played a role to modulate the wavy root morphology.⁷In our previous experiments for studying the light-induced wavy roots, rice seedlings were cultured in water. In order to reveal the effect of interaction between light signal pathway and touch stimuli on rice seminal root growth, the sterilized rice seeds of TCN1 and TNG67 cultivars were germinated at 30°C in dark for 2 d and moved to continuous white light conditions (90 µmol m⁻² s⁻¹) to grow in vertically oriented square dishes containing 1.5% and 2% (w/v) Phytagel (Sigma, St. Louis, MO), respectively. The Phytagel percentage of the medium that we used here were higher than that was used for plant tissue culture in usual. After 3 d culture, the seminal roots of seedlings on 1.5% Phytagel performed wavy phenotype that was similar to the wavy roots observed in water-cultured seedlings under light conditions. Furthermore, the seminal roots in 2% Phytagel was grown to be a curling type (Fig. 1). On the other hand, no wavy or curling root morphology was presented in dark conditions either in 1.5% or 2% Phytagel-containing medium (Fig. 1). These results showed that root-Phytagel interaction could not directly induce the significant wavy or curling root morphology under dark growth conditions, but it could modify the light-stimulated helical growth and conduct the curling root morphology.Open in a separate windowFigure 1Effect of the interaction between light signals and touch stimuli on seminal root growth in rice seedlings. The TCN1 rice seeds were germinated in dark for 2 d and then germinated seeds were transferred to 1.5% and 2% Phytagel-containing plates for continuously growing. The root morphology was investigated after 3 d of Phytagelculture under light and dark conditions.Photomorphology of the seminal roots was diverse among rice varieties. Our previous data showed light-induced wavy roots could not be conducted in TNG67 rice cultivar.³ Here, we also observed the root growth of TNG67 rice seedlings on Phytagel-containing plates, and the results showed the straight root morphology in both light and dark conditions (data not shown). These results indicated that the phenomena of touch-stimulated curling roots were also rice variety-dependent.Based on above mentioned results, it was suggested that mechanisms of root-gel interaction for conducting curling phenotype was highly correlated with the transduction pathway of light signal to induce root waving. This hypothesis was supported by the observation on physiological mechanisms of light-induced wavy roots in rice plants and the obstacle-touching stimulated wavy roots in Arabidopsis. Our previous observation in rice plants suggested that auxin polar transport was essential for light-induced root waving and fatty acid oxygenation was involved to the mechanism of root waving in light.³ In Arabidopsis, auxin polar transport was also indicated to play a role in obstacle-touching stimulated root waving.^8,9 In addition, wavy roots of Arabidopsis could be induced by several products of fatty acid oxygenation, i.e., ketols, ketones and hydroxides.¹⁰In conclusion, both light signal and touch stimuli were the important environmental cues to guide root growth and determine root morphology. Touch stimuli were able to modify the trajectory of light-induced root waving. Phenomena of both light-induced wavy roots and touch-stimulated curling roots were rice variety-dependent. Furthermore, it was suggested that touch-induced signaling may be associated with the light-induced signal pathway to conduct curling phenotype in seminal roots of rice seedlings.     

Microbial Resolution of Racemic 2- and 3-Alkylcyclohexanols

By using microorganisms (their esterase), (±)-trans and cis-2-methylcyclohexyl acetates were asymmetrically hydrolyzed to (?)-trans-2-methylcyc]ohexanol with (+)-trans-2-methyl-cyclohexyl acetate and (?)-cis-2-methylcyclohexanol with (+)-cis-2-methylcyclohexyl acetate. Similarly (±)-trans and cis-3-methylcyclohexyl acetates were hydrolyzed by the same microorganisms to give (+)-trans-3-methylcyclohexanol with (?)-trans-3-methylcyclohexyl acetate and (?)-cis-3-methylcyclohexanol with (+)-cis-3-methylcyclohexyl acetate.     

The blue light receptor Phototropin 1 suppresses lateral root growth by controlling cell elongation

We investigated the relationship between the blue light receptor phototropin 1 (phot1) and lateral root growth in Arabidopsis thaliana seedlings. Fluorescence and confocal microscopy images, as well as PHOT1 mRNA expression studies provide evidence that it is highly expressed in the elongation zone of lateral roots where auxin is accumulating. However, treatment with the auxin transport inhibitor N‐1‐naphthylphthalamic acid significantly reduced PHOT1 expression in this zone. In addition, PHOT1 expression was higher in darkness than in light. The total number of lateral roots was higher in the phot1 mutant than in wild‐type Arabidopsis. Cells in the elongation zone of lateral roots of the phot1 mutant were longer than those of wild‐type lateral roots. These findings suggest that PHOT1 plays a role(s) in elongation of lateral roots through the control of an auxin‐related signalling pathway.     

Reactive oxygen species localization in roots of <Emphasis Type="Italic">Arabidopsis thaliana</Emphasis> seedlings grown under phosphate deficiency

Arabidopsis plants responding to phosphorus (P) deficiency increase lateral root formation and reduce primary root elongation. In addition the number and length of root hairs increases in response to P deficiency. Here we studied the patterns of radical oxygen species (ROS) in the roots of Arabidopsis seedlings cultured on media supplemented with high or low P concentration. We found that P availability affected ROS distribution in the apical part of roots. If plants were grown on high P medium, ROS were located in the root elongation zone and quiescent centre. At low P ROS were absent in the elongation zone, however, their synthesis was detected in the primary root meristem. The proximal part of roots was characterized by ROS production in the lateral root primordia and in elongation zones of young lateral roots irrespective of P concentration in the medium. On the other hand, plants grown at high or low P differed in the pattern of ROS distribution in older lateral roots. At high P, the elongation zone was the primary site of ROS production. At low P, ROS were not detected in the elongation zone. However, they were present in the proximal part of the lateral root meristem. These results suggest that P deficiency affects ROS distribution in distal parts of Arabidopsis roots. Under P-sufficiency ROS maximum was observed in the elongation zone, under low P, ROS were not synthesized in this segment of the root, however, they were detected in the apical root meristem.     

Intermittent exposure to traces of green leaf volatiles triggers the production of (Z)-3-hexen-1-yl acetate and (Z)-3-hexen-1-ol in exposed plants

Intermittent exposure during a period of 3 weeks of undamaged Arabidopsis plants to trace amounts of volatiles emitted by freshly damaged Arabidopsis plants resulted in an increase of subsequent artificial-damage-induced production of (Z)-3-hexen-1-yl acetate and (Z)-3-hexen-1-ol in the exposed Arabidopsis plants when compared with Arabidopsis plants exposed to undamaged Arabidopsis plant volatiles (control plants). We previously showed that (Z)-3-hexen-1-yl acetate attracts a parasitic wasp, Cotesia glomerata. Thus, the induced production of this volatile explained our previously reported finding that, when artificially damaged, the exposed plants were more attractive to C. glomerata than control plants.     

Root responses of Quercus ilex L. seedlings to drought and fire

Abstract

Drought treatments in holm-oak (Quercus ilex) seedlings induce variations in total root length, number of root apices, shoot/root dry weight, and root electrolyte leakage. When drought treatments last for more than 50 days a considerable number of fine lateral roots die, irrespective of branching order or distribution within the root system. Scorching of drought-treated seedlings induces a transient stimulation of root growth. These results indicate that root turnover is deeply affected during treatments, with survival of seedlings being entrusted to the tolerance of a number of roots situated in the deeper region of the root system. Activity of the meristematic tissue present within the apices of these surviving roots supports regeneration of above-ground lost organs during recovery. Knowledge of the mechanisms ensuring the survival of Mediterranean tree seedlings following drought and fire is useful for developing models of vegetation dynamics.     

(−)-Epilamprolobine and its N-oxide,lupin alkaloids from Sophora tomentosa

From the fresh leaves of Sophora tomentosa, three new lupin alkaloids, (?)-epilamprolobine, (+)-epilamprolobine N-oxide and 5-(3′-methoxycarbonylbutyroyl)aminomethyl-trans-quinolizidine N-oxide, have further been isolated along with (+)-matrine, (+)-matrine N-oxide, (+)-sophocarpine N-oxide, (?)-anagyrine, (?)- baptifoline, (?)-cytisine, (?)-N-methylcytisine, (?)-N-formylcytisine, (?)-N-acetylcytisine and (±)-ammodendrine. The absolute configurations of (+)-epilamprolobine N-oxide (1R:5R:6S) and (?)-epilamprolobine (5R:6S) have also been established by spectroscopic data and by comparison with synthetic (+)-epilamprolobine (5S:6R)derived from (?)-lupinine (5R:6R). (?)-Epilamprolobine is a diastereomer of (+)-lamprolobine (5R:6R) in Lamprolobium fruticosum and 5-(3′-methoxycarbonylbutyroyl) aminomethyl-trans-quinolizidine N-oxide is presumed to be an artefact. A biosynthetic pathway for the formation of (?)-epilamprolobine is also proposed.     

Concise Total Synthesis of Acortatarin A

(+) and (?)-Dihydropinidine and (+)- and (?)-epidihydropinidine were synthesized from hydroxy esters 1 and 2 which had been prepared by yeast reduction of methyl (2-oxocyclohexyl)acetate. The enantiomeric excess at the C-1 positions of 1 and 2 were both determined as more than 99% ee.