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PubMed1992

UV light stress induces the synthesis of the early light-inducible protein and prevents its degradation.

ELIP is a nuclear-encoded protein localized in the thylakoid membranes. The protein is specifically induced by blue light in mature, light-grown plants (Adamska, I., Ohad, I., and Kloppstech, K. (1992) Proc. Natl. Acad. Sci. U. S. A. 89, 2610-2613), as well as in plants developed in the light in which pigment synthesis and plastid development were inhibited by the bleaching herbicide norflurazon. ELIP transcription and protein accumulation are induced also by UVA but not by UVB light. However, UVB light allows ELIP synthesis induced by superimposed white light. The protein is stable under light stress including UVA and UVB light, but it is rapidly degraded upon cessation of the light stress conditions. ELIP synthesis and integration into the chloroplast membranes is related neither to chloroplast translation activity nor to photosynthetic electron flow. Inhibition of carotenoid synthesis by fluridone, a bleaching herbicide which causes extensive damage to the photosynthetic apparatus, does not affect induction of ELIP transcription during light stress but greatly enhances ELIP accumulation. Based on these results it is proposed that ELIP turnover is related to the light stress and recovery process in plants.

Arabidopsis Proteins↗
PubMed1986

Reverse reaction of smooth muscle myosin light chain kinase. Formation of ATP from phosphorylated light chain plus ADP.

Incubation of smooth muscle phosphorylated heavy meromyosin in the presence of myosin light chain kinase, calmodulin, ADP, and Ca2+ results in a decrease of the protein-bound phosphate. The dephosphorylation is not due to phosphatase activity and is dependent on the presence of ADP and the active ternary myosin light chain kinase complex. Using 32P-labeled phosphorylated 20,000-dalton light chains as the phosphate donor, the formation of ATP from ADP can be demonstrated. This reaction requires the presence of Ca2+, calmodulin, and myosin light chain kinase. These results indicate that myosin light chain kinase can catalyze a reverse reaction and form ATP from ADP and phosphorylated substrate. The rate of the reverse reaction, kcat/KLC approximately 0.21 min-1 microM-1, is considerably slower than the forward reaction under similar conditions and is therefore detectable only at relatively high concentrations of myosin light chain kinase. For the reverse reaction, KmADP is approximately 30 microM and ATP is a competitive inhibitor, KIATP approximately 88 microM. For the forward reaction, measured with both isolated light chains and intact myosin, KmATP is approximately 100 microM and ADP is a competitive inhibitor, KiADP approximately 140 microM (myosin) and 120 microM (light chains). Thus, the affinity of ATP for the forward and reverse reactions is similar, but the affinity of ADP is higher for the reverse reaction. From the light chain dependence of the two reactions, the following was calculated: forward, Km = 5 microM, kcat = 1720 min-1, and reverse, Km = 130 microM, kcat = 27 min-1. In contrast to the data obtained with isolated light chains, it is suggested that, with intact myosin as substrate, the Km term is primarily responsible for determining the rate of the reverse reaction. With light chains phosphorylated at serine 19 and threonine 18, it was shown that both sites act as a phosphate donor, although the reverse reaction for threonine 18 is slower than that for serine 19.

Adenosine Diphosphate↗
PubMed1975

Characterization of light chain and light chain constant region fragment mRNAs in MPC 11 mouse myeloma cells and variants.

Cultured MPC 11 mouse myeloma cells synthesize not only gamma2b heavy and kappa light chains but also a carboxyl terminal (constant region) fragment of kappa light chain. In vitro translational analysis of total cytoplasmic and microsomal RNA indicates that these cells contain RNA which directs synthesis of both a light chain precursor and a light chain fragment precursor. Variant clones which do not synthesize either heavy or light chains continue to synthesize the light chain fragment. One such "nonproducing" variant was studied in detail. It does not contain translatable mRNA for the intact light chain but does contain RNA which is translated into the light chain fragment precursor. Nucleic acid hybridization analysis with a cDNA probe specific for the constant region of kappa light chains revealed that microsomal RNA from the wild-type cell contains both 14S and a 10S species of kappa specific RNA, whereas the variant contains only the 10S species. Translational analysis of these same RNAs indicates that the 14S species codes for the light chain precursor, while the 10S RNA codes for the light chain fragment precursor.

Animals↗
PubMed2005

Light therapy for seasonal affective disorder with blue narrow-band light-emitting diodes (LEDs).

BACKGROUND: While light has proven an effective treatment for Seasonal Affective Disorder (SAD), an optimal wavelength combination has not been determined. Short wavelength light (blue) has demonstrated potency as a stimulus for acute melatonin suppression and circadian phase shifting. METHODS: This study tested the efficacy of short wavelength light therapy for SAD. Blue light emitting diode (LED) units produced 468 nm light at 607 microW/cm2 (27 nm half-peak bandwidth); dim red LED units provided 654 nm at 34 microW/cm2 (21 nm half-peak bandwidth). Patients with major depression with a seasonal pattern, a score of > or =20 on the Structured Interview Guide for the Hamilton Depression Rating Scale-SAD version (SIGH-SAD) and normal sleeping patterns (routine bedtimes between 10:00 pm and midnight) received 45 minutes of morning light treatment daily for 3 weeks. Twenty-four patients completed treatment following random assignment of condition (blue vs. red light). The SIGH-SAD was administered weekly. RESULTS: Mixed-effects analyses of covariance determined that the short wavelength light treatment decreased SIGH-SAD scores significantly more than the dimmer red light condition (F = 6.45, p = .019 for average over the post-treatment times). CONCLUSIONS: Narrow bandwidth blue light at 607 microW/cm2 outperforms dimmer red light in reversing symptoms of major depression with a seasonal pattern.

Adult↗
PubMed1981

An immunological approach to myosin light-chain function in thick filament linked regulation. 1. Characterization, specificity, and cross-reactivity of anti-scallop myosin heavy- and light-chain antibodies by competitive, solid-phase radioimmunoassay.

Antibodies specific for the regulatory light-chain (R-LC), "essential" light-chain (SH-LC), heavy-chain, and rod fragment of myosin from the striated adductor muscle of scallop (Aequipecten irradians) were prepared and characterized. A competitive, solid-phase radioimmunoassay on microtiter plates, a combination of two systems described earlier by Kuettner et al. [Kuettner, M. G., Wang, A. L., & Nisonoff, A. (1972) U. Exp. Med. 135, 579-595] and Klinman et al. [Klinman, N. R., Pickard, A. R., Sigal N. H., Gearhart, P. J., Metcalf, E. S., & Pierce, S. K. (1976) Ann. Immunol. (Paris) 127C, 489-502], was adapted and used for an immunological survey of different myosins and myosin light chains. Anti-myosin light-chain antibodies were specific for the homologous chain and did not cross-react with the heterologous one, i.e., regulatory and essential light chains of scallop myosin could be distinguished immunologically. These antibodies also had a high degree of species specificity. A partial cross-reactivity was obtained only for the light chains of two closely related molluscan species out of the over thirty invertebrate or vertebrates species tested. Two populations of anti-SH-LC antibodies were found which differed in their ability to abolish regulation of scallop myofibrils and also in their immunological reactivity with cyanogen bromide fragments of teh SH-LC. A comparison of the cross-reactivity of the intact SH-LC with its CNBr fragments showed that most antigenic sites of the SH-LC were available to the antibodies. Free light chains and light chains associated with myosin reacted with antibodies in a very similar manner, indicating that the association of the light chains with myosin may not be accompanied by major conformational changes. Antibodies against scallop myosin heavy chain and rod fragment cross-reacted to a variable extent with all invertebrate myosins but with none of the vertebrates species tested. The antibodies did not cross-react with platelet and Physarum myosins. The heavy and light chains of myosin from scallop striated adductor, mantle, and foot were found toi be immunologically identical, whereas myosin from smooth adductor showed some differences mainly in the heavy-chain portion which forms the subfragment-l region of the myosin molecule. Heavy and light chains of scallop heart muscle myosin differed significantly from those of striated adductor muscle. Cross-reactivity did not depend on the regulatory properties of myosin.

Animals↗
PubMed1992

Ethylene is not involved in the blue light-induced growth inhibition of red light-grown peas.

Although the growth of intact plants is inhibited by irradiation with blue light, the growth rate of isolated stem segments is largely unaffected by blue light. We hypothesized that this loss of responsiveness was a result of ethylene production as part of the wounding response. However, we found no interaction between ethylene- and blue light-induced growth inhibition in dark- or red light-grown seedlings of pea (Pisum sativum L.). Inhibition of growth begins in dark-grown seedlings exposed to blue light within 3 min of the onset of blue light, as was known for red light-grown seedlings. By contrast, ethylene-induced inhibition of growth occurs only after a lag of 20 to 30 min or more (dark-grown seedlings) or 60 min (red light-grown seedlings). Also, the inhibition response of red light-grown seedlings is the same whether ethylene is present from the onset of continuous blue-light treatment or not. Finally the spatial distribution of inhibition following blue light was different from that following ethylene treatment.

Journal Article↗
PubMed1966

Potentiation of photosynthetic oxygen evolution in red light by small quantities of monochromatic blue light.

Growth of the giant unicellular green alga, Acetabularia crenulata, stops in red light of broad spectral composition, but can be restored by the addition of small quantities of blue light. Long-term records of O(2) evolution indicate that the photosynthesis of Acetabularia responds in a parallel manner to blue light. Cells photosynthesizing at a light-limited rate in white light were given red light at an intensity that served to match or somewhat increase the instantaneous rate of O(2) production. A rapid decline in the rate commenced within 15 minutes and continued for 2 hours or more until it had fallen to 20 to 40% of the initial level. Very small doses of violet or blue radiation (<10(-8) Einstein/cm(2)) then affected a complete, though temporary, restoration of the original rate of photosynthesis. Responses began after a lag of 4 to 5 minutes, regardless of their magnitude, and in the most favorable instances persisted 4 to 6 hours after the stimulus. Blue light treatments were effective as flashes as brief as 2.5 seconds, given simultaneously or in sequence with the red measuring light, or as low-intensity continuous irradiations. Blue-light induction of the response was stable over at least 5 minutes of darkness. After a suitable red-light pretreatment, 2 other algae, Chlamydomonas reinhardi and Fucus vesiculosus, were shown to respond similarly to low-intensity irradiations with blue or blue-green light.Crude action spectra were determined for the response of Acetabularia to short wavelength irradiations given simultaneously or sequentially with the red measuring light. Two peaks of effectiveness were found, one near 450 mmu, and another, as yet ill defined, in the near UV. The data suggest a shoulder around 490 mmu. All wavelengths above 540 mmu were entirely ineffective.

Journal Article↗
PubMed1988

Enhancement of the Stomatal Response to Blue Light by Red Light, Reduced Intercellular Concentrations of CO(2), and Low Vapor Pressure Differences.

The effects of environmental parameters on the blue light response of stomata were studied by quantifying transient increases in stomatal conductance in Commelina communis following 15 seconds by 0.100 millimole per square meter per second pulses of blue light. Because conductance increases were not observed following red light pulses of the same or greater (30 seconds by 0.200 millimole per square meter per second) fluences, the responses observed could be reliably attributed to the specific blue light response of the guard cells, rather than to guard cell chlorophyll. In both Paphiopedilum harrisianum, which lacks guard cell chloroplasts, and Commelina, the blue light response was enhanced by 0.263 millimole per square meter per second continuous background red light. Thus, the blue light response and its enhancement do not require energy derived from red-light-driven photophosphorylation by the guard cell chloroplasts. In Commelina, reduction of the intercellular concentration of CO(2) by manipulation of ambient CO(2) concentrations resulted in an enhanced blue light response. In both Commelina and Paphiopedilum, the blue light response was decreased by an increased vapor pressure difference. The magnitude of blue-light-specific stomatal opening thus appears to be sensitive to environmental conditions that affect the carbon and water status of the plant.

Journal Article↗
PubMed1981

Subunit function in cardiac myosin. Effects of binding phosphorylated and unphosphorylated myosin light chain 2 to light chain 2-deficient myosin.

The 20,000-dalton light chain of cardiac muscle myosin can be specifically digested and thereby removed from the rest of the myosin molecule by incubation with a myofibrillar protease (Malhotra, A., Huang, S., and Bhan, A. (1979) Biochemistry 18, 461-467). In order to study the effects of phosphorylation of the 20,000-dalton myosin light chain, experiments were carried out with cardiac muscle myosin that was made deficient in this light chain following proteolysis. Both the phosphorylated and unphosphorylated isolated 20,000-dalton myosin light chain of cardiac muscle myosin were found to bind to light chain-deficient myosin. Prior to readdition of the isolated light chains, this light chain-deficient myosin was found to have a higher MgATPase activity in the presence and absence of actin, than native myosin. Binding of the unphosphorylated myosin light chain restored the MgATPase activity of light chain-deficient myosin to that of native cardiac myosin. In contrast, the binding of 2 mol of the previously phosphorylated myosin light chain did not lower the actin-activated MgATPase activity. The results suggest that while phosphorylation of the 20,000-dalton light chain of cardiac muscle myosin is not essential for the actin-activated MgATPase activity, it may have a modulatory role.

Animals↗
PubMed1996

Phytochrome A enhances the promotion of hypocotyl growth caused by reductions in levels of phytochrome B in its far-red-light-absorbing form in light-grown Arabidopsis thaliana.

We sought to determine if phytochrome B (phyB)-mediated responses to the red light (R)/far-red light (FR) ratio are affected by phytochrome A (phyA) activity in light-grown seedlings of Arabidopsis thaliana. Pulses of FR delayed into the dark period were less effective than end-of-day (EOD) FR in promoting hypocotyl growth over a given period in darkness. White light minus blue light interposed instead of darkness between the end of the white-light photoperiod and the FR pulse was sufficient to maintain responsivity to the decrease in phyB in FR-light-absorbing form in wild-type (WT) seedlings, but not in the phyA mutant. Compared with EOD R, hourly R+FR pulses provided throughout the night caused a stronger promotion of stem growth than a single EOD R+FR pulse in WT Arabidopsis, cucumber, mustard, sunflower, tobacco, and tomato, but not in phyA Arabidopsis or in the aurea mutant of tomato. WT seedlings of Arabidopsis responded to a range of high EOD R/FR ratios, whereas the phyA mutant required stronger reductions in the EOD R/FR ratio. In sunlight, phyA seedlings of Arabidopsis showed no response to the "early warning" signals of neighboring vegetation, and hypocotyl-growth promotion occurred at higher plant densities than in the WT. Thus, under a series of light conditions, the sensitivity or responsivity to reductions in the R/FR ratio were larger in WT than in phyA seedlings. A product of phyA is therefore proposed to enhance the hypocotyl-growth response to decreases in phyB in FR-light-absorbing form in light grown seedlings.

Arabidopsis↗
PubMed2001

Dissection of the light signal transduction pathways regulating the two early light-induced protein genes in Arabidopsis.

The expression of light-regulated genes in plants is controlled by different classes of photoreceptors that act through a variety of signaling molecules. During photomorphogenesis, the early light-induced protein (Elip) genes are among the first to be induced. To understand the light signal transduction pathways that regulate Elip expression, the two Elip genes, Elip1 and Elip2, in Arabidopsis were studied, taking advantage of the genetic tools available for studying light signaling in Arabidopsis. Using two independent quantitative reverse transcriptase-PCR techniques, we found that red, far-red, and blue lights positively regulate expression of the Elip genes. Phytochrome A and phytochrome B are involved in this signaling. The cryptochrome or phototropin photoreceptors are not required for blue-light induction of either Elip gene, suggesting the involvement of an additional, unidentified, blue-light receptor. Although the COP9 signalosome, a downstream regulator, is involved in dark repression of both Elips, Elip1 and Elip2 show different expression patterns in the dark. The transcription factor HY5 promotes the light induction of Elip1, but not Elip2. A defect in photosystem II activity in greening of hy5 seedlings may result from the loss of Elip1. Heat shock positively controlled Elip1 and Elip2 in a light-independent fashion. This induction is independent of HY5, indicating that heat shock and light activate transcription of the Elip genes through independent pathways.

Arabidopsis↗
PubMed2002

Dental curing lights--maintenance of visible light curing units.

Successful curing depends directly on many factors of which the most important is the correct functioning of the curing unit to emit light of sufficient intensity and quality. If the contribution of any of these factors is at a less than adequate level, the light-sensitive materials will not polymerise completely, which in the long term may be responsible for secondary caries and decreased longevity of the restoration. Factors which may reduce the light output include ageing of the bulb and filter, damage of the light guide or fibre optics, deposits on the light tip due to composite build-up or autoclave scale, erosion of light tip surface due to immersion sterilisation, and line voltage fluctuations. Recent studies carried out to investigate the effectiveness of curing lights in clinical use show that most practitioners are unaware of the importance of routine monitoring, care and maintenance of curing lights. This paper reviews some of the available literature on the monitoring, care and maintenance of curing lights, including information on the influence that some of these may have on the intensity emitted by the curing light.

Dental Materials↗
PubMed1993

Level dependent signal flow in the light pupil reflex. II. Phase velocity of responses to sinusoidal light stimuli.

Pupillary responses to sinusoidal light stimuli were measured over a range of light levels and frequencies. The phase lag and equivalent time delay of these responses were reduced in an approximately log-linear fashion with increasing mean light level (slope = -60 ms/log unit). The magnitude of this level dependence is reduced at higher frequencies, and at higher light levels. This nonlinear level dependent signal flow (LDSF) effect is shown to be essentially independent of target distance (accommodative stimulus) which influences pupil size, and of pupil size itself. Thus most of the level dependence probably resides in the afferent path of the light-pupil reflex arc, before the accommodation signal joins the light signal in the Edinger-West-phal nucleus. A systems model is presented to the LDSF effect described here and in the companion papers (Myers and Stark 1993a, b). When parameters of the model are adjusted to fit pupillary responses to transient light stimuli over a range of light levels, the model simulates reduced phase lag in response to increased mean light level, and the reduction in this LDSF effect with increased mean light level or increasing stimulus frequency without further changes in parameters. This latter reduction explains the relatively small level dependence seen in latency data (-34 ms/log unit). These data will be shown (Myers and Stark 1990b) to be commensurate with reduction in pupil cycle time (increased frequency of oscillation) observed in high gain oscillation experiments as mean brightness increases.(ABSTRACT TRUNCATED AT 250 WORDS)

Accommodation, Ocular↗
PubMed1998

Total radiated power, infrared output, and heat generation by cold light sources at the distal end of endoscopes and fiber optic bundle of light cables.

BACKGROUND: Skin burns and ignition of drapes have been reported with the use of cold light sources. The aim of the study was to document the temperature generated by cold light sources and to correlate this with the total radiated power and infrared output. METHODS: The temperature, total radiated power, and infrared output were measured as a function of time at the end of the endoscope (which is inserted into the operative field) and the end of the fiber optic bundle of the light cable (which connects the cable to the light port of the endoscope) using halogen and xenon light sources. RESULTS: The highest temperature recorded at the end of the endoscope was 95 degrees C. The temperature measured at the optical fiber location of the endoscope was higher than at its lens surface (p < 0.0001). At the end of the fiber optic bundle of light cables, the temperature reached 225 degrees C within 15 s. The temperature recorded at the optical fiber location of all endoscopes and light cables studied rose significantly over a period of 10 min to reach its maximum (p <0.0001) and then leveled off for the duration of the study (30 min). The infrared output accounted only for 10% of the total radiated power. CONCLUSIONS: High temperatures are reached by 10 min at the end of fiber optic bundle of light cables and endoscopes with both halogen and xenon light sources. This heat generation is largely due to the radiated power in the visible light spectrum.

Cold Temperature↗
PubMed2006

Effective single-charge end point of cordless light-emitting diode light-curing units.

INTRODUCTION: The purpose of this study was to evaluate the battery lives of cordless light-emitting diodes (LEDs) and their effect on orthodontic bracket bond strength. METHODS: One hundred eighty-six metal orthodontic brackets were bonded to extracted molars. Two LED light-curing units (L. E. Demetron [SDS/Kerr, Orange, Calif] and Ortholux [3M Unitek, Monrovia, Calif]) were evaluated. Each light was used to bond 93 specimens. One bracket was bonded every 5 minutes until the battery ran out. The lights were activated for 20 seconds, then automatically turned off for 40 seconds every minute (33% duty cycle) without recharging. Bonded specimens were stored in water at 37 degrees C for 24 hours and then subjected to shear force with a universal testing machine until bracket failure. RESULTS: Repeated measures ANOVA detected significantly weaker mean shear bond strength and fewer consecutive cures with the Ortholux compared with the L. E. Demetron light-curing unit. However, when the first 5 time points were excluded, there were no differences between the 2 lights, demonstrating that the lights performed similarly after the first 20 minutes of operation Just before battery failure, both lights still provided the same power density as at the beginning. CONCLUSIONS: Both light-curing units provided adequate power density for up to 2 hours without recharging at a 33% duty cycle. There was no significant decrease in power in cordless LED light-curing units as the battery life approached its end point.

Analysis of Variance↗
PubMed2003

Ca2+ binding to myosin regulatory light chain affects the conformation of the N-terminus of essential light chain and its binding to actin.

We prepared a new type of skeletal myosin subfragment 1 (S1-MLC1F) containing both, the essential and the regulatory light chains, intact, by exchanging the essential light chains of papain S1 with bacterially expressed longer isoform (MLC1F) of this light chain. We then compared the enzymatic and structural properties of chymotryptic S1, papain S1, and S1-MLC1F in the presence and in the absence of Ca(2+) ions bound to the regulatory light chain. In the presence of Ca(2+), subfragment 1 containing both intact light chains exhibited lower V(max) and lower K(m) for actin activation of S1 ATPase. When S1-MLC1F was cross-linked to actin via the N-terminus of the essential light chain, the yield was much higher when Ca(2+) ions saturated the regulatory light chain. Limited proteolysis of the essential light chain in S1-MLC1F was significantly inhibited in the presence of calcium as compared to chymotryptic S1. We conclude that the effect of binding of Ca(2+) to the regulatory light chain is transmitted to the N-terminal extension of the longer isoform of the essential light chain. The resulting structure of the N-terminus is less susceptible to proteolytic digestion, binds tighter to actin, and has an inhibitory effect on actin-activated myosin ATPase. This new conformation of the N-terminus may be responsible for calcium induced myosin-linked modulation of striated muscle contraction.

Actins↗
PubMed2003

Behavioral arousal blocks light-induced phase advances in locomotor rhythmicity but not light-induced Per1 and Fos expression in the hamster suprachiasmatic nucleus.

Both photic and nonphotic stimuli entrain circadian rhythms. Although the adaptive significance of nonphotic clock resetting is unknown, one possibility is that nonphotic cues modulate circadian responses to light. Results of studies on the interaction between photic and nonphotic stimuli support this idea. During the day, light blocks the effects of nonphotic stimuli on the phase of locomotor rhythms and on expression of clock genes in suprachiasmatic nucleus (SCN) neurons. At night, novelty-induced activity prior to and during exposure to light attenuates the phase-shifting response to that light, but the effects of this manipulation on clock gene expression are unknown. The present experiments explore the interaction between behavioral state and response to light at the molecular level. We show that confining hamsters to novel wheels immediately after a light pulse during the late subjective night attenuates light-induced phase advances of wheel-running rhythms and the transient effects on circadian period. In contrast to the striking effect of novelty-induced activity on behavioral responses to light, Fos protein and Per1 mRNA were robustly expressed in the SCN of all light-pulsed animals, regardless of behavioral treatment. Our results are inconsistent with the idea that light and nonphotic stimuli block each other's effects on phase shifts by inducing or attenuating transcription of Per1. Photic regulation of clock genes and spontaneous rhythmic expression of clock genes are probably mediated by different mechanisms.

Animals↗
PubMed2001

POR C of Arabidopsis thaliana: a third light- and NADPH-dependent protochlorophyllide oxidoreductase that is differentially regulated by light.

During the sequencing of the genome of Arabidopsis thaliana a gene has been identified that encodes a novel NADPH-protochlorophyllide oxidoreductase (POR)-like protein (accession number AC 002560). This protein has been named POR C. We have expressed the POR C protein in Escherichia coli and have determined its in vitro activity. POR C shows the characteristics of a light-dependent and NADPH-requiring POR similar to POR A and POR B. The expression of the POR C gene differs markedly from that of the POR A and POR B genes. In contrast to the POR A and POR B mRNAs, the POR C mRNA has been shown previously to accumulate only after the beginning of illumination. In light-adapted mature plants only POR B and POR C mRNAs were detectable. The amounts of both mRNAs show pronounced diurnal rhythmic fluctuations. While the oscillations of POR B mRNA are under the control of the circadian clock, those of POR C mRNA are not. Another difference between POR B and POR C was found in seedlings that were grown under continuous white light. The concentration of POR C mRNA rapidly declined and soon dropped beyond the limit of detection, after these seedlings were transferred to the dark. On the other hand. POR B mRNA was unaffected by this light/dark shift. When seedlings were exposed to different light intensities, the amounts of POR B mRNA remained the same, while POR A and POR C mRNAs were modulated in an inverse way by these light intensity changes. POR A mRNA was still detectable in seedlings grown under low light intensities but disappeared at higher light intensities, while the mRNA concentration of POR C rose with increasing light intensities. These different responses to light suggest that the functions of the three PORs of Arabidopsis are not completely redundant, but may allow the plant to adapt its needs for chlorophyll biosynthesis more selectively by using preferentially one of the three enzymes under a given light regime.

Adaptation, Physiological↗