Speed of signal transfer in the chloroplast accumulation response

Chloroplast photorelocation movement is important for plants to perform efficient photosynthesis. Phototropins were identified as blue-light receptors for chloroplast movement in Arabidopsis thaliana and in the fern Adiantum capillus-veneris, whereas neochrome functions as a dual red/blue light receptor in the latter. However, the signal transduction pathways involved in chloroplast movement remain to be clarified. To investigate the kinetic properties of signalling from these photoreceptors to the chloroplasts, we deduced the speed of signal transfer using Adiantum capillus-veneris gametophytes. When a region of dark-adapted gametophyte cells was subjected to microbeam irradiation, chloroplasts moved towards the irradiated area even in subsequent darkness. We therefore recorded the movement and calculated the speeds of signal transfer by time-lapse imaging. Movement speeds under red or blue light were similar, e.g., about 1.0 μm min⁻¹ in prothallial cells. However, speeds varied according to cell polarity in protonemal cells. The speed of signal transfer from the protonemal apex to the base was approximately 0.7 μm min⁻¹, but roughly 2.3 μm min⁻¹ in the opposite direction. The speed of signal transfer in Arabidopsis thaliana mesophyll cells was approximately 0.8 μm min⁻¹ by comparison. Surprisingly, chloroplasts located farthest away from the microbeam were found to move faster than those in close proximity to the site of irradiation both in Adiantum capillus-veneris and A. thaliana.     

Temperature-dependent binding to the thylakoid membranes of nuclear-coded chloroplast heat-shock proteins

Two nuclear-coded heat-shock proteins (HSP) of pea (Pisum sativum) are synthesized as larger precursors of 26 kDa and 30 kDa in vitro. They are transported post-translationally into isolated, homologous chloroplasts where they are processed to mature proteins of 22 kDa and 25 kDa, respectively. When the chloroplasts used for the transport are isolated from control plants grown at 25 degrees C the 22-kDa and 25-kDa HSPs are located in the stroma of the chloroplasts. However, when chloroplasts are prepared from heat-shocked plants both proteins are found bound to the thylakoid membranes. The transition of the non-binding to the binding status is comparatively sharp and occurs between 36 degrees C and 40 degrees C in the variety 'Rosa Krone'. The transition temperature has been determined at 38 degrees C for 'Rosa Krone' and at 40 degrees C for the variety 'Golf'. At 42 degrees C, 15-min treatment of the plants is sufficient to induce membrane binding, which persists for at least 4-6 h (but not for 24 h) after return to the ambient temperature. Once lost, membrane binding can be reinduced by a second heat-shock treatment in vivo. High light intensities during the heat shock interfere with the binding capacity for heat-shock proteins.     

Temperature-dependent sugar accumulation in interspecific Capsicum F1 plants showing hybrid weakness

Journal of Plant Research - In plants, F1 hybrids showing hybrid weakness exhibit weaker growth than their parents. The phenotypes of hybrid weakness are often suppressed at certain temperatures....     

Kinetics of EPR signal IIvf in chloroplast Photosystem II

The risetime of EPR signal II_vf (S II_vf) has been measured in oxygen-evolving Photosystem II particles from spinach chloroplasts at pH 6.0. The EPR signal shows an instrument-limited rise upon induction ($\text{t}{}_{\mathrm{<mtext>1</mtext><mtext>2</mtext>}}\text{? 3 μ}\text{s}$). These data are consistent with a model where the species Z responsible for S II_vf is the immediate electron donor to P-680⁺ in spinach chloroplasts. A new, faster decay component of S II_vf has also been detected in these experiments.     

Functional characterization of recombinant chloroplast signal recognition particle

The signal recognition particle (SRP) is a ubiquitous system for the targeting of membrane and secreted proteins. The chloroplast SRP (cpSRP) is unique among SRPs in that it possesses no RNA and is functional in post-translational as well as co-translational targeting. We have expressed and purified the two components of the Arabidopsis thaliana chloroplast signal recognition particle (cpSRP) involved in post-translational transport: cpSRP54 and the chloroplast-specific protein, cpSRP43. Recombinant cpSRP supports the efficient in vitro insertion of pea preLhcb1 into isolated thylakoid membranes. Recombinant cpSRP is a stable heterodimer with a molecular mass of approximately 100 kDa as determined by analytical ultracentrifugation, gel filtration analysis, and dynamic light scattering. The interactions of the components of the recombinant heterodimer and pea preLhcb1 were probed using an immobilized peptide library (pepscan) approach. These data confirm two previously reported interactions with the L18 region and the third transmembrane helix of Lhcb1 and suggest that the interface of the cpSRP43 and cpSRP54 proteins is involved in substrate binding. Additionally, cpSRP components are shown to recognize peptides from the cleavable, N-terminal chloroplast transit peptide of preLhcb1. The interaction of cpSRP43 with cpSRP54 was probed in a similar experiment with a peptide library representing cpSPR54. The C terminus of cpSRP54 is essential for the formation of the stable cpSRP complex and cpSPR43 interacts with distinct regions of the M domain of cpSRP54.     

Rise time of EPR signal IIvf in chloroplast Photosystem II

The rise time of the photoinduced, reversible EPR Signal II_vf in spinach chloroplasts is found using flash excitation to be 20 ± 10 μs. The results are interpreted as evidence that the Signal II_vf radical is an electron carrier on the donor side of Photosystem II, but probably does not result from the first donor to P680⁺.     

Temperature-dependent dry receptor on antenna ofPeriplaneta. Tonic response

Summary Identified as a dry receptive unit by transitory impulse frequencies up to about 200 imp/sec during rapid drops in humidity (Fig. 3) and which no other modality elicited, the dry unit on the antenna ofPeriplaneta americana is characterized by a regular (Fig. 4) and relatively high stationary impulse frequency (10–65 imp/s). Without exception the stationary discharge rate (tonic frequency) rose with falling values of stationary absolute humidity at constant temperature, and with rising values of stationary temperature of ambient air at constant humidity. Enthalpy and evaporation cooling appear to be ruled out as exclusive adequate explanations for this double dependence. No matter whether tonic frequency is plotted against absolute humidity based on either volume of moist air or weight of dry air, or against partial pressure of water vapor in ambient air, or the difference between saturation and partial vapor pressure, or against relative humidity, the dependence on the temperature is not eliminated (Figs. 5–7). Because a temperature range of about 20 °C and all humidities between 0 and 100% occupy the same large segment of the unit's tonic frequency spectrum (Fig. 8), the unit is termed bimodal.The author wishes to express indebtedness and gratitude to Prof. Dr. Hansjochem Autrum for backing the early stages of this project with the assistance of the Deutsche Forschungsgemeinschaft, to Prof. Dr. Helmut Altner for his prolonged support, to Dr. Hans-Jürgen Hinz for his helpful discussion of questions involving thermodynamics, to Prof. Dr. Friedrich Earth for helpful criticism of the text, and to Miss Christel Praeg for tireless technical assistance.     

Monokaryotic chloroplast mutation has no effect on non-Mendelian transmission of chloroplast and mitochondrial DNA in Chlamydomonas species

Summary. We studied whether the monokaryotic chloroplast (moc) mutation affects the transmission of chloroplast and mitochondrial DNA in Chlamydomonas species. We used a previously isolated moc mutant from our cell line G33, which had only one large chloroplast nucleus. To obtain zygotes we crossed the mutant cells with wild-type cells, and mutant cells with receptive mates (females [mt+] with males [mt–]). In these zygotes, we recorded preferential dissolution of mt– parental chloroplast nuclei and fusion of the two cell nuclei. Antibiotic-resistance markers of chloroplast DNA were maternally transmitted in all crosses. PCR analysis of the cytochrome b (cob) gene sequence showed that the mitochondrial DNA was paternally transmitted to offspring. These results suggest that the moc mutation did not affect the organelle DNA transmission.Correspondence and reprints: Laboratory of Cell and Functional Biology, Faculty of Science, University of the Ryukyus, Nishihara, Okinawa, 903-0213, Japan.     

Extensive methylation of chloroplast DNA by a nuclear gene mutation does not affect chloroplast gene transmission in chlamydomonas

Based on analysis by high pressure liquid chromatography, greater than 35% of the cytosine residues in chloroplast DNA of vegetative cells were found to be methylated constitutively in the nuclear gene mutation (me-1) of Chlamydomonas reinhardtii, which has an otherwise wild-type phenotype. Digestion of chloroplast DNA from vegetative cells and gametes of this mutant with restriction endonucleases Hpa II and Msp I reveals that in the 5′CCGG3′ sequence, CpG is methylated extensively, whereas CpC is only methylated occasionally. Hae III (5′GGCC3′) digestion of the mutant chloroplast DNA also shows extensive methylation of the GpC sequence. In contrast to the results of Sager and colleagues, which show a correlation between methylation of chloroplast DNA and transmission of chloroplast genes in crosses, our results with crosses of the me-1 mutant suggest that extensive chloroplast DNA methylation may be insufficient to account for the pattern of inheritance of chloroplast genes in Chlamydomonas.     

Synchronization and signal transmission in protoplasmic strands ofPhysarum

Isolated protoplasmic strands ofPhysarum polycephalum, mounted as a trapeze, show synchronous contraction activities when the isometric tension development of both arms of the trapeze is measured independently of each other. This phase regulation can be experimentally disturbed by temperature changes. Within a permanent gradient, however, the phases become resynchronized. The maximal temperature gradient between both arms allowing a phase resynchronization was approximately 9° C along a distance of 25 mm. The transmission of the signal along the middle piece of the trapeze (which, as the connecting part of both arms, is responsible for signal transmission in phase synchronization) can be influenced by temperature changes. The minimal temperature allowing a signal transmission is 15° C, the maximal temperature approximately 29° C. A morphological investigation of protoplasmic strands mounted as trapezes revealed that the normal architecture of the objects is not influenced by the experimental trapeze arrangement. Permanent thermal gradients induce thermotactic reactions, i.e., a preferred protoplasmic mass transport into one arm of the trapeze. This leads, after several hours, to a morphological asymmetry of the trapeze. In spite of the fact that this reaction limits the temporal use of trapezes within thermal gradients to 2–3 h, the capacity of such strands for phase regulation is not hindered. Thermal gradients are suitable methods for studying the unknown phase-regulating factor and its transmission. As criteria for an intact pathway of signal transmission, the capacity of the trapeze arms to resynchronize as well as to maintain synchronization within a thermal gradient can be used.Dedicated to A. Frey-Wyssling on the occasion of his 80^th birthday on November 8^th, 1980     

A chloroplast envelope-transfer sequence functions as an export signal in Escherichia coli

The small subunit precursor of pea ribulose-1,5-bisphosphate carboxylase/oxygenase engineered with prokaryotic elements was expressed in Escherichia coli. This resulted in a dependable level of synthesis of the precursor protein in E. coli. The bacterially synthesised plant precursor protein was translocated from the cytoplasm and targeted to the outer membrane of the envelope zone. During the translocation step, a significant proportion of the precursor was processed to a soluble, mature SSU and found localised in the periplasm. The determined amino acid sequence of the isolated precursor showed that it had a deletion of an arginine residue at position -15 in the transit peptide. Expression of this transit peptide-appended mammalian cytochrome b(5) in E. coli displayed a targeting profile of the chromogenic chimera that was similar to that observed with the plant precursor protein.     

Concerted complex assembly and GTPase activation in the chloroplast signal recognition particle

The universally conserved signal recognition particle (SRP) and SRP receptor (SR) mediate the cotranslational targeting of proteins to cellular membranes. In contrast, a unique chloroplast SRP in green plants is primarily dedicated to the post-translational targeting of light harvesting chlorophyll a/b binding (LHC) proteins. In both pathways, dimerization and activation between the SRP and SR GTPases mediate the delivery of cargo; whether and how the GTPase cycle in each system adapts to its distinct substrate proteins were unclear. Here, we show that interactions at the active site essential for GTPase activation in the chloroplast SRP and SR play key roles in the assembly of the GTPase complex. In contrast to their cytosolic homologues, GTPase activation in the chloroplast SRP-SR complex contributes marginally to the targeting of LHC proteins. These results demonstrate that complex assembly and GTPase activation are highly coupled in the chloroplast SRP and SR and suggest that the chloroplast GTPases may forego the GTPase activation step as a key regulatory point. These features may reflect adaptations of the chloroplast SRP to the delivery of their unique substrate protein.     

Assembly of chloroplast signal recognition particle involves structural rearrangement in cpSRP43

Signal recognition particle in chloroplasts (cpSRP) exhibits the unusual ability to bind and target full-length proteins to the thylakoid membrane. Unlike cytosolic SRPs in prokaryotes and eukaryotes, cpSRP lacks an RNA moiety and functions as a heterodimer composed of a conserved 54-kDa guanosine triphosphatase (cpSRP54) and a unique 43-kDa subunit (cpSRP43). Assembly of the cpSRP heterodimer is a prerequisite for post-translational targeting activities and takes place through interactions between chromatin modifier domain 2 (CD2) of cpSRP43 and a unique 10-amino-acid region in cpSRP54 (cpSRP54_pep). We have used multidimensional NMR spectroscopy and other biophysical methods to examine the assembly and structure of the cpSRP43-cpSRP54 interface. Our data show that CD2 of cpSRP43 binds to cpSRP54_pep in a 1:1 stoichiometry with an apparent K_d of ∼ 1.06 μM. Steady-state fluorescence and far-UV circular dichroism data suggest that the CD2-cpSRP54_pep interaction causes significant conformational changes in both CD2 and the peptide. Comparison of the three-dimensional solution structures of CD2 alone and in complex with cpSRP54_pep shows that significant structural changes are induced in CD2 in order to establish a binding interface contributed mostly by residues in the N-terminal segment of CD2 (Phe5-Val10) and an arginine doublet (Arg536 and Arg537) in the cpSRP54 peptide. Taken together, our results provide new insights into the mechanism of cpSRP assembly and the structural forces that stabilize the functionally critical cpSRP43-cpSRP54 interaction.     

Reliability of signal transmission in stochastic nerve axon equations

We introduce a method for computing probabilities for spontaneous activity and propagation failure of the action potential in spatially extended, conductance-based neuronal models subject to noise, based on statistical properties of the membrane potential. We compare different estimators with respect to the quality of detection, computational costs and robustness and propose the integral of the membrane potential along the axon as an appropriate estimator to detect both spontaneous activity and propagation failure. Performing a model reduction we achieve a simplified analytical expression based on the linearization at the resting potential (resp. the traveling action potential). This allows to approximate the probabilities for spontaneous activity and propagation failure in terms of (classical) hitting probabilities of one-dimensional linear stochastic differential equations. The quality of the approximation with respect to the noise amplitude is discussed and illustrated with numerical results for the spatially extended Hodgkin-Huxley equations. Python simulation code is supplied on GitHub under the link https://github.com/deristnochda/Hodgkin-Huxley-SPDE.     

Synchronization and signal transmission in protoplasmic strands of Physarum

The importance of endoplasmic streaming in the synchronization of contraction activites in plasmodial strands of Physarum was investigated under experimental conditions allowing simultaneous observation of the endoplasmic flow in the middle part of a strand mounted as a trapeze and the measurement of isometric contraction activities of the arms of the trapeze, as well as of the activities of the strand portion connecting the arms. The correlation of longitudinal and radial contraction activities in different regions of a trapeze was examined. Whereas the arms and the middle part of a trapeze contract synchronously in a longitudinal direction (in-phase behaviour), an antiphase correlation appeared when comparing the longitudinal contraction activity of the arms and the radial activity of the middle part. This result is interpreted to mean that the middle part is able to perform isotonic contractions which induce radial dilatation of the strands. No clear-cut correlation between longitudinal and radial activities could be found when measuring simultaneously both activities in one and the same arm of a trapeze by combining tensiometry and cinematography. Protoplasmic shuttle streaming within a strand mounted as a trapeze is found to run regularly out of one arm through the middle part into the other arm, and vice versa. There is no correlation between the time points of streaming reversal and a certain stage of contraction cycles as presented by the contraction curves of the arms. However, there is a good correlation between the points of streaming reversal and the phase deviations of the longitudinal contraction activities of the arms. The importance of these phase deviations for the control of streaming reversal, i.e., for the generation of hydrostatic pressure differences in a system working with phase synchrony, is discussed. The role of endoplasmic streaming as a pacemaker for synchronization phenomena of contraction activities is stressed. The possibility is discussed that shuttle streaming of endoplasm acts as a mechanical coupling within the regulation phenomena resulting in spatial monorhythmicity.Partly presented at the Cell Motility workshop, 8^th European Muscle Conference, Heidelberg 17.–20. September 1979