Carotenoids In Light-harvesting Complexes Research Articles

Carotenoid responds to excess energy dissipation in the LH2 complex from Rhodoblastus acidophilus.

The functions of both (bacterio) chlorophylls and carotenoids in light-harvesting complexes have been extensively studied during thepast decade, yet, the involvement of BChl a high-energy Soret band in the cascade of light-harvesting processes still remainsa relatively unexplored topic. Here, we present transient absorption data recorded after excitation of the Soret band in the LH2 complex from Rhodoblastus acidophilus. Comparison of obtained data to those recorded after excitation of rhodopin glucoside and B800 BChl a suggests that no Soret-to-Car energy transfer pathway is active in LH2 complex. Furthermore, a spectrally rich pattern observed in the spectral region of rhodopin glucoside ground state bleaching (420-550nm) has been assigned toanelectrochromic shift. The results of global fitting analysis demonstrate two more features. A 6ps component obtained exclusively after excitation of the Soret band has been assigned to the response of rhodopin glucoside to excess energy dissipation in LH2. Another time component, ~ 450ps, appearing independently of theexcitation wavelength was assigned to BChla-to-Car triplet-triplet transfer. Presented data demonstrate several new features of LH2 complex and its behavior following the excitation of the Soret band.

Engineering purple bacterial carotenoid biosynthesis to study the roles of carotenoids in light-harvesting complexes.

Carotenoids are important photosynthetic pigments that play key roles in light harvesting and energy transfer, photoprotection, and in the folding, assembly, and stabilization of light-harvesting pigment-protein complexes. The genetically tractable purple phototrophic bacteria have been useful for investigating the biosynthesis and function of photosynthetic pigments and cofactors, including carotenoids. Here, we give an overview of the roles of carotenoids in photosynthesis and of their biosynthesis, focusing on the extensively studied purple bacterium Rhodobacter sphaeroides as a model organism. We provide detailed procedures for manipulating carotenoid biosynthesis, and for the preparation and analysis of the light-harvesting and photosynthetic reaction center complexes that bind them. Using appropriate examples from the literature, we discuss how such approaches have enhanced our understanding of the biosynthesis of carotenoids and the photosynthesis-related functions of these fascinating molecules.

The influence of light regime on the growth data and pigment composition of the plant Gentiana lutea cultured in vitro

New technologies of reintroduction of plant species presuppose implementing both traditional and biotechnological methods for obtaining certain planting materials. However, plants cultivated in vitro exist in specific conditions that lead to changes in their structural and functional state. This explains why it is hard for them to adapt to ex vitro and in situ conditions. Therefore, there is a need for the development of a multistage method of cultivating in vitro plants that would make the influence on their adaptive mechanism in ex vitro and in situ conditions possible. One of its stages is the optimization of the light regime of cultivation which can both initiate the change of the state of the photosynthetic apparatus of plants and increase their bioproductivity stimulating the work of their protective system. This work studies changes in the morphogenesis, growth data and pigment composition of the rare species of Gentiana lutea L. of three populations in the Ukrainian Carpathian (mountains Pozhyzhevska and Sheshul-Pavlyk, plateau Lemska) in vitro focusing particularly on the cultivation light regime. The research has proved the inefficiency of using fluorescent lamps of daylight lamps (LD) type as source of illumination because the low intensity of luminous flux in the area of photosynthetically active radiation (PAR), as well as high proportion of wavelength of blue (400–500 nm) and green (500–600 nm) range in the spectrum cause specific reactions of photomorphogenesis, which, despite the high content of pigments in plastids, lead to poor development of root systems, stretching the stems, formation of small leaves with thin leaflet plate, generally low productivity and low adaptive potential of G. lutea plants to ex vitro and in situ conditions. Complement of cold white light lamps to the fluorescent lamps LD type in the ratio of 1 : 1 enables one to increase the intensity of illumination in the field of PAR and raise the fraction of wavelength of red range (600–700 nm). Such light conditions both improve the bio-productivity of G. lutea plants of all three populations cultured in vitro in comparison to the LD type regimen, reducing the content of chlorophyll b and carotenoids in light-harvesting complexes of photosystems and facilitate an increase in the microclonal multiplication factor without using higher concentrations of exogenous growth regulators,which significantly reduces the cost of the process of obtaining planting materials. It was proved that a combination of LD type lamps, cold white light lamps and phytolamps in the ratio 1 : 1 : 0.6 should be used on the final stages of preparation of the planting material of G. lutea before transferring it to ex vitro and in situ conditions. This relates to the fact that the increase of the wavelength of the red range results in the widening of the active surface of the leaves, rise in the content of photosynthetic pigments, and the noticeable growth of the aboveground and underground parts of the plants. The article assumes that the use of such illumination mode will ensure a faster transition of cultured in vitro G. lutea plants from heterotrophic to autotrophic nutrition, improving their adaptive potential and enabling easier adaptation to non-sterile ex vitro and in situ conditions.

Origin of the S* Excited State Feature of Carotenoids in Light-Harvesting Complex 1 from Purple Photosynthetic Bacteria.

This spectroscopic study investigates the origin of the transient feature of the S* excited state of carotenoids bound in LH1 complexes from purple bacteria. The studies were performed on two RC-LH1 complexes from Rba. sphaeroides strains that bound carotenoids with different carbon-carbon double bond conjugation N, neurosporene (N = 9) and spirilloxanthin (N = 13). The S* transient spectral feature, originally associated with an elusive and optically silent excited state of spirilloxanthin in the LH1 complex, may be successfully explained and mimicked without involving any unknown electronic state. The spectral and temporal characteristics of the S* feature suggest that it is associated with triplet-triplet annihilation of carotenoid triplets formed after direct excitation of the molecule via a singlet fission mechanism. Depending on pigment homogeneity and carotenoid assembly in the LH1 complex, the spectro-temporal component associated with triplet-triplet annihilation may simply resolve a pure T-S spectrum of a carotenoid. In some cases (like spirilloxanthin), the T-S feature will also be accompanied by a carotenoid Stark spectrum and/or residual transient absorption of minor carotenoid species bound into LH1 antenna complex.

Excitation energy transfer from the bacteriochlorophyll Soret band to carotenoids in the LH2 light-harvesting complex from Ectothiorhodospira haloalkaliphila is negligible.

Pathways of intramolecular conversion and intermolecular electronic excitation energy transfer (EET) in the photosynthetic apparatus of purple bacteria remain subject to debate. Here we experimentally tested the possibility of EET from the bacteriochlorophyll (BChl) Soret band to the singlet S2 level of carotenoids using femtosecond pump-probe measurements and steady-state fluorescence excitation and absorption measurements in the near-ultraviolet and visible spectral ranges. The efficiency of EET from the Soret band of BChl to S2 of the carotenoids in light-harvesting complex LH2 from the purple bacterium Ectothiorhodospira haloalkaliphila appeared not to exceed a few percent.

Evaluating the Nature of So-Called S*-State Feature in Transient Absorption of Carotenoids in Light-Harvesting Complex 2 (LH2) from Purple Photosynthetic Bacteria.

Carotenoids are a class of natural pigments present in all phototrophic organisms, mainly in their light-harvesting proteins in which they play roles of accessory light absorbers and photoprotectors. Extensive time-resolved spectroscopic studies of these pigments have revealed unexpectedly complex photophysical properties, particularly for carotenoids in light-harvesting LH2 complexes from purple bacteria. An ambiguous, optically forbidden electronic excited state designated as S* has been postulated to be involved in carotenoid excitation relaxation and in an alternative carotenoid-to-bacteriochlorophyll energy transfer pathway, as well as being a precursor of the carotenoid triplet state. However, no definitive and satisfactory origin of the carotenoid S* state in these complexes has been established, despite a wide-ranging series of studies. Here, we resolve the ambiguous origin of the carotenoid S* state in LH2 complex from Rba. sphaeroides by showing that the S* feature can be seen as a combination of ground state absorption bleaching of the carotenoid pool converted to cations and the Stark spectrum of neighbor neutral carotenoids, induced by temporal electric field brought by the carotenoid cation–bacteriochlorophyll anion pair. These findings remove the need to assign an S* state, and thereby significantly simplify the photochemistry of carotenoids in these photosynthetic antenna complexes.

On photoprotective mechanisms of carotenoids in light harvesting complex

Carotenoids in light harvesting complex (LHC) play an important role in preventing plants photodamage caused by excess light. Non-photochemical quenching (NPQ) is an important mechanism adopted by plants to deal with high light intensity and the major component is referred to as energy dependent quenching (qE). Despite numerous studies have been devoted to investigating the site and mechanism of qE, there are still much debate on these topics. In this article, we discussed the possible site and underlying mechanism of qE based on the structural similarity of carotenoids. Moreover, being as good antioxidants, carotenoids’ potential protective effects against LHC photo-oxidation by quenching active oxygen species or triplet excited state chlorophyll are also discussed.

Excited-State Dynamics of Carotenoids in Light-Harvesting Complexes. 1. Exploring the Relationship between the S1 and S* States

Dispersed transient absorption spectra collected at variable excitation intensities in combination with time-resolved signals were used to explore the underlying connectivity of the electronic excited-state manifold of the carotenoid rhodopin glucoside in the light-harvesting 2 complex isolated from Rhodopseudomonas acidophila. We find that the S state, which was recently identified as an excited state in carotenoids bound in bacterial light-harvesting complexes, exhibits a different response to the increase of excitation intensity than the S(1) state, which suggests that the models used so far to describe the excited states of carotenoids are incomplete. We propose two new models that can describe both the time-resolved and the intensity-dependent data; the first postulates that S(1) and S* are not populated in parallel after the decay of the initially excited S(2) state but instead result from the excitation of distinct ground-state subpopulations. The second model introduces a resonantly enhanced light-induced transition during excitation, which promotes population to higher-lying excited states that favors the formation of S* over S(1). Multiwavelength target analysis of the time-resolved and excitation-intensity dependence measurements were used to characterize the involved states and their responses. We show that both proposed models adequately fit the measured data, although it is not possible to determine which model is most apt. The physical origins and implications of both models are explored.

More on the catalysis of internal conversion in chlorophyll a by an adjacent carotenoid in light-harvesting complex (Chl a/ b LHCII) of higher plants: time-resolved triplet-minus-singlet spectra of detergent-perturbed complexes

Wavelength-selective photo-excitation of samples containing a detergent and LHCII (the main light-harvesting complex pertaining to photosystem II of green plants) is used for recording time-resolved triplet-minus-singlet (TmS) difference spectra, with a view to probing interactions between chlorophyll a (Chl a) and chlorophyll b (Chl b), and between Chl a and lutein (Lut). Once the detergent concentration ( C D) exceeds a threshold, C ©, the TmS spectrum becomes sensitive to λ ⊗, the wavelength of excitation, and to t, the delay between excitation and observation. Each increment in C D brings about a diminution in the efficiency of a †→ x † transfer (triplet–triplet transfer from Chl a to Lut) and a rise in both the triplet formation yield and the fluorescence yield of Chl a. What is more, b*→ a* transfer (singlet–singlet transfer from Chl b to Chl a) slackens to such an extent that Chl b*→Chl b † intersystem crossing, negligible when C D is below C ©, begins to vie with transfer, for the deactivation of Chl b* (in the foregoing an asterisk/dagger denotes singlet/triplet excitation). The reduction in the efficiencies of the two transfers is easily understood by: (i) invoking the Kühlbrandt–Wang–Fujiyoshi model of LHCII, which posits each Chl b in contact with a Chl a and each Chl a in contact with a Lut, and (ii) assuming that the detergent severs contact between adjacent chromophores. That a growth in the triplet yield of Chl a* accompanies the detergent-induced decrease in the efficiency of a †→ x † transfer becomes intelligible if one assumes, further, that internal conversion in Chla * is faster than that in Chla * , where under or over lining betokens the presence or absence of a carotenoid neighbour. When C D is close to C ©, most Chl a molecules are adjacent to a Lut, internal conversion dominates, and the overall triplet yield is low. As C D is gradually raised the Chla → Chla transformation sets in, causing concomitant drops in the efficiencies of a †→ x † transfer and internal conversion, and a consequent rise in the overall yields of Chl a fluorescence and formation of Chl a triplets.

Quenching of chlorophyll a singlets and triplets by carotenoids in light-harvesting complex of photosystem II: comparison of aggregates with trimers

Laser-induced changes in the absorption spectra of isolated light-harvesting chlorophyll a/ b complex (LHC II) associated with photosystem II of higher plants have been recorded under anaerobic conditions and at ambient temperature by using multichannel detection with sub-microsecond time resolution. Difference spectra (Δ A) of LHC II aggregates have been found to differ from the corresponding spectra of trimers on two counts: (i) in the aggregates, the carotenoid (Car) triplet–triplet absorption band (Δ A>0) is red-shifted and broader; and (ii) the features attributable to the perturbation of the Q y band of a chlorophyll a (Chl a) by a nearby Car triplet are more pronounced, than in trimers. Aggregation, which is known to be accompanied by a reduction in the fluorescence yield of Chl a, is shown to cause a parallel decline in the triplet formation yield of Chl a; on the other hand, the efficiency (100%) of Chl a-to-Car transfer of triplet energy and the lifetime (9.3 μs) of Car triplets are not affected by aggregation. These findings are rationalized by postulating that the antenna Cars transact, besides light-harvesting and photoprotection, a third process: energy dissipation within the antenna. The suggestion is advanced that luteins, which are buried inside the LHC II monomers, as well as the other, peripheral, xanthophylls (neoxanthin and violaxanthin) quench the excited singlet state of Chl a by catalyzing internal conversion, a decay channel that competes with fluorescence and intersystem crossing; support for this explanation is presented by recalling reports of similar behaviour in bichromophoric model compounds in which one moiety is a Car and the other a porphyrin or a pyropheophorbide.

Reconstitution of the Bacterial Core Light-harvesting Complexes of Rhodobacter sphaeroides and Rhodospirillum rubrum with Isolated α- and β-Polypeptides, Bacteriochlorophyll a, and Carotenoid

Methodology has been developed to reconstitute carotenoids and bacteriochlorophyll alpha with isolated light-harvesting complex I (LHI) polypeptides of both Rhodobacter sphaeroides and Rhodospirillum rubrum. Reconstitution techniques first developed in this laboratory using the LHI polypeptides of R. rubrum, R. sphaeroides, and Rhodobacter capsulatus reproduced bacteriochlorophyll alpha spectral properties characteristic of LHI complexes lacking carotenoids. In this study, carotenoids are supplied either as organic-solvent extracts of chromatophores or as thin-layer chromatography or high performance liquid chromatography-purified species. The resulting LHI complexes exhibit carotenoid and bacteriochlorophyll a spectral properties characteristic of native LHI complexes of carotenoid-containing bacteria. Absorption and circular dichroism spectra support the attainment of a native-like carotenoid environment in the reconstituted LHI complexes. For both R. sphaeroides- and R. rubrum-reconstituted systems, fluorescence excitation spectra reveal appropriate carotenoid to bacteriochlorophyll alpha energy-transfer efficiencies based on comparisons with the in vivo systems. In the case of R. rubrum reconstitutions, carotenoids afford protection from photodynamic degradation. Thus, carotenoids reconstituted into LHI exhibit spectral and functional characteristics associated with native pigments. Heterologous reconstitutions demonstrate the applicability of the developed assay in dissecting the molecular environment of carotenoids in light-harvesting complexes.