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Publications (10 of 19) Show all publications
Nanda, S., Shutova, T., Cainzos, M., Bag, P., Jansson, S. & Holzwarth, A. R. (2024). ChloroSpec: A new in vivo chlorophyll fluorescence spectrometer for simultaneous wavelength- and time-resolved detection. Physiologia Plantarum, 176(2), Article ID e14306.
Open this publication in new window or tab >>ChloroSpec: A new in vivo chlorophyll fluorescence spectrometer for simultaneous wavelength- and time-resolved detection
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2024 (English)In: Physiologia Plantarum, ISSN 0031-9317, E-ISSN 1399-3054, Vol. 176, no 2, article id e14306Article in journal (Refereed) Published
Abstract [en]

Chlorophyll fluorescence is a ubiquitous tool in basic and applied plant science research. Various standard commercial instruments are available for characterization of photosynthetic material like leaves or microalgae, most of which integrate the overall fluorescence signals above a certain cut-off wavelength. However, wavelength-resolved (fluorescence signals appearing at different wavelengths having different time dependent decay) signals contain vast information required to decompose complex signals and processes into their underlying components that can untangle the photo-physiological process of photosynthesis. Hence, to address this we describe an advanced chlorophyll fluorescence spectrometer - ChloroSpec - allowing three-dimensional simultaneous detection of fluorescence intensities at different wavelengths in a time-resolved manner. We demonstrate for a variety of typical examples that most of the generally used fluorescence parameters are strongly wavelength dependent. This indicates a pronounced heterogeneity and a highly dynamic nature of the thylakoid and the photosynthetic apparatus under actinic illumination. Furthermore, we provide examples of advanced global analysis procedures integrating this three-dimensional signal and relevant information extracted from them that relate to the physiological properties of the organism. This conveniently obtained broad range of data can make ChloroSpec a new standard tool in photosynthesis research.

Place, publisher, year, edition, pages
John Wiley & Sons, 2024
National Category
Botany
Identifiers
urn:nbn:se:umu:diva-223953 (URN)10.1111/ppl.14306 (DOI)001207485500001 ()38659135 (PubMedID)2-s2.0-85191196422 (Scopus ID)
Funder
The Kempe FoundationsSwedish Research CouncilKnut and Alice Wallenberg FoundationSwedish Foundation for Strategic Research
Available from: 2024-05-03 Created: 2024-05-03 Last updated: 2025-02-14Bibliographically approved
Bag, P., Shutova, T., Shevela, D., Lihavainen, J., Nanda, S., Ivanov, A. G., . . . Jansson, S. (2023). Flavodiiron-mediated O2 photoreduction at photosystem I acceptor-side provides photoprotection to conifer thylakoids in early spring. Nature Communications, 14(1), Article ID 3210.
Open this publication in new window or tab >>Flavodiiron-mediated O2 photoreduction at photosystem I acceptor-side provides photoprotection to conifer thylakoids in early spring
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2023 (English)In: Nature Communications, E-ISSN 2041-1723, Vol. 14, no 1, article id 3210Article in journal (Refereed) Published
Abstract [en]

Green organisms evolve oxygen (O2) via photosynthesis and consume it by respiration. Generally, net O2 consumption only becomes dominant when photosynthesis is suppressed at night. Here, we show that green thylakoid membranes of Scots pine (Pinus sylvestris L) and Norway spruce (Picea abies) needles display strong O2 consumption even in the presence of light when extremely low temperatures coincide with high solar irradiation during early spring (ES). By employing different electron transport chain inhibitors, we show that this unusual light-induced O2 consumption occurs around photosystem (PS) I and correlates with higher abundance of flavodiiron (Flv) A protein in ES thylakoids. With P700 absorption changes, we demonstrate that electron scavenging from the acceptor-side of PSI via O2 photoreduction is a major alternative pathway in ES. This photoprotection mechanism in vascular plants indicates that conifers have developed an adaptative evolution trajectory for growing in harsh environments.

Place, publisher, year, edition, pages
Springer Nature, 2023
National Category
Biochemistry Molecular Biology Botany
Identifiers
urn:nbn:se:umu:diva-209538 (URN)10.1038/s41467-023-38938-z (DOI)001002562700001 ()37270605 (PubMedID)2-s2.0-85160880215 (Scopus ID)
Funder
EU, Horizon 2020, 675006Swedish Research Council, (2016-04894 aSwedish Research Council, 2021-05062Swedish Research Council, 2020-03809The Kempe Foundations, 2014Swedish Research Council Formas, 2015-00907Swedish Research Council Formas, 2021-01474Swedish Foundation for Strategic Research, FFF20- 0008Vinnova, 2016-00504Knut and Alice Wallenberg Foundation, 2016-0352Knut and Alice Wallenberg Foundation, 2020.0240Göran Gustafsson Foundation for Research in Natural Sciences and Medicine, BS2022-0021
Available from: 2023-06-13 Created: 2023-06-13 Last updated: 2025-02-20Bibliographically approved
Lihavainen, J., Šimura, J., Bag, P., Fataftah, N., Robinson, K. M., Delhomme, N., . . . Jansson, S. (2023). Salicylic acid metabolism and signalling coordinate senescence initiation in aspen in nature. Nature Communications, 14(1), Article ID 4288.
Open this publication in new window or tab >>Salicylic acid metabolism and signalling coordinate senescence initiation in aspen in nature
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2023 (English)In: Nature Communications, E-ISSN 2041-1723, Vol. 14, no 1, article id 4288Article in journal (Refereed) Published
Abstract [en]

Deciduous trees exhibit a spectacular phenomenon of autumn senescence driven by the seasonality of their growth environment, yet there is no consensus which external or internal cues trigger it. Senescence starts at different times in European aspen (Populus tremula L.) genotypes grown in same location. By integrating omics studies, we demonstrate that aspen genotypes utilize similar transcriptional cascades and metabolic cues to initiate senescence, but at different times during autumn. The timing of autumn senescence initiation appeared to be controlled by two consecutive “switches”; 1) first the environmental variation induced the rewiring of the transcriptional network, stress signalling pathways and metabolic perturbations and 2) the start of senescence process was defined by the ability of the genotype to activate and sustain stress tolerance mechanisms mediated by salicylic acid. We propose that salicylic acid represses the onset of leaf senescence in stressful natural conditions, rather than promoting it as often observed in annual plants.

Place, publisher, year, edition, pages
Springer Nature, 2023
National Category
Botany
Identifiers
urn:nbn:se:umu:diva-212477 (URN)10.1038/s41467-023-39564-5 (DOI)001037322100027 ()37463905 (PubMedID)2-s2.0-85165262787 (Scopus ID)
Funder
Swedish Research CouncilSwedish Research Council FormasThe Kempe FoundationsSwedish Foundation for Strategic ResearchKnut and Alice Wallenberg FoundationVinnova
Available from: 2023-08-03 Created: 2023-08-03 Last updated: 2025-04-24Bibliographically approved
Arshad, R., Saccon, F., Bag, P., Biswas, A., Calvaruso, C., Bhatti, A. F., . . . Büchel, C. (2022). A kaleidoscope of photosynthetic antenna proteins and their emerging roles. Plant Physiology, 189(3), 1204-1219
Open this publication in new window or tab >>A kaleidoscope of photosynthetic antenna proteins and their emerging roles
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2022 (English)In: Plant Physiology, ISSN 0032-0889, E-ISSN 1532-2548, Vol. 189, no 3, p. 1204-1219Article in journal (Refereed) Published
Abstract [en]

Photosynthetic light-harvesting antennae are pigment-binding proteins that perform one of the most fundamental tasks on Earth, capturing light and transferring energy that enables life in our biosphere. Adaptation to different light environments led to the evolution of an astonishing diversity of light-harvesting systems. At the same time, several strategies have been developed to optimize the light energy input into photosynthetic membranes in response to fluctuating conditions. The basic feature of these prompt responses is the dynamic nature of antenna complexes, whose function readily adapts to the light available. High-resolution microscopy and spectroscopic studies on membrane dynamics demonstrate the crosstalk between antennae and other thylakoid membrane components. With the increased understanding of light-harvesting mechanisms and their regulation, efforts are focusing on the development of sustainable processes for effective conversion of sunlight into functional bio-products. The major challenge in this approach lies in the application of fundamental discoveries in light-harvesting systems for the improvement of plant or algal photosynthesis. Here, we underline some of the latest fundamental discoveries on the molecular mechanisms and regulation of light harvesting that can potentially be exploited for the optimization of photosynthesis.

Place, publisher, year, edition, pages
Oxford University Press, 2022
National Category
Botany
Identifiers
urn:nbn:se:umu:diva-194031 (URN)10.1093/plphys/kiac175 (DOI)000790909500001 ()35512089 (PubMedID)2-s2.0-85133103283 (Scopus ID)
Funder
EU, Horizon 2020, 675006
Available from: 2022-04-22 Created: 2022-04-22 Last updated: 2023-03-23Bibliographically approved
Bag, P. (2022). How could Christmas trees remain evergreen?: photosynthetic acclimation of Scots pine and Norway spruce needles during winter. (Doctoral dissertation). Umeå: Umeå University
Open this publication in new window or tab >>How could Christmas trees remain evergreen?: photosynthetic acclimation of Scots pine and Norway spruce needles during winter
2022 (English)Doctoral thesis, comprehensive summary (Other academic)
Alternative title[sv]
Hur kan julgranen vara grön? : fotosyntesapparatens anpassning till vinterförhållanden hos tall och gran
Abstract [en]

Plants and other green organisms harvest sunlight by green chlorophyll pigments and covertit to chemical energy (sugars) and oxygen in a process called photosynthesis providing the foundation for life on Earth. Although it is unanimously believed that oceanic phytoplanktons are the main contributors to the global photosynthesis, the contribution of coniferous boreal forests distributed across vast regions of the northern hemisphere cannot be undermined. Hence boreal forests account signifificantly for social, economical and environmental sustainability. Not only do conifers thrive in the tundra regions with extreme climate, but they also maintain their needles green over the boreal winter. A question remains; what makes them so resilient? In this respect, we aimed to understand the remarkable winter adaptation strategies in two dominant boreal coniferous species,i.e., Pinus sylvestris and Picea abies. First, we mapped the transcriptional landscape in Norway spruce (Picea abies) needles over the annual cycle. Transcriptional changes in the nascent needles reflflected a sequence of developmental processes and active vegetative growth during early summer and summer. Later after maturation, transcriptome reflflected activated defense against biotic factors and acclimationin response to abiotic environmental cues such as freezing temperatures during winter. Secondly, by monitoring the photosynthetic performance of Scot pine needles, we found that the trees face extreme stress during the early spring (Feb-Mar) when sub-zero temperatures are accompanied by high solar radiation. At this time, drastic changes occur in the thylakoid membranes of the chloroplast that allows the mixing of photosystem I and photosystem II that typically remain laterally segregated. This triggers direct energy transfer from PSII to PSI and thus protects PSII from damage. Furthermore, we found that this loss of lateral segregation may be a consequence of triple phosphorylationof Lhcb1 (Light harvesting complex1 of photosystem II). The structural changes in thylakoid membranes also lead to changes inthe thylakoid macro domain organisationand pigment protein composition. Furthermore, we discovered that while PSII is protected by direct energy transfer, the protection of PSI is provided through photoreduction of oxygen by flavodiiron proteins, which in turn allows P700 to stay in an oxidised state necessary for direct energy transfer. These coordinated cascades of changes concomitantly protect both PSI and PSII to maintain the needles green over the winter.

Place, publisher, year, edition, pages
Umeå: Umeå University, 2022. p. 65
Keywords
Scots Pine, Norway spruce, Photosynthesis, Winter adaptation
National Category
Biochemistry Molecular Biology Bioinformatics and Computational Biology Botany Biophysics Evolutionary Biology
Research subject
biological chemistry; biology; Molecular Biology; Physiological Botany
Identifiers
urn:nbn:se:umu:diva-194032 (URN)978-91-7855-788-2 (ISBN)978-91-7855-787-5 (ISBN)
Public defence
2022-05-20, Lilla hörsalen, KBC huset, Umeå, 09:30 (English)
Opponent
Supervisors
Note

On page 12, List of papers, manuscripts (in preparation): Athor names hidden due to copyright - see printed version. 

Available from: 2022-04-29 Created: 2022-04-22 Last updated: 2025-02-20Bibliographically approved
Fataftah, N., Edlund, E., Lihavainen, J., Bag, P., Björkén, L., Näsholm, T. & Jansson, S. (2022). Nitrate fertilization may delay autumn leaf senescence, while amino acid treatments do not. Physiologia Plantarum, 174(3), Article ID e13690.
Open this publication in new window or tab >>Nitrate fertilization may delay autumn leaf senescence, while amino acid treatments do not
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2022 (English)In: Physiologia Plantarum, ISSN 0031-9317, E-ISSN 1399-3054, Vol. 174, no 3, article id e13690Article in journal (Refereed) Published
Abstract [en]

Fertilization with nitrogen (N)-rich compounds leads to increased growth but may compromise phenology and winter survival of trees in boreal regions. During autumn, N is remobilized from senescing leaves and stored in other parts of the tree to be used in the next growing season. However, the mechanism behind the N fertilization effect on winter survival is not well understood, and it is unclear how N levels or forms modulate autumn senescence. We performed fertilization experiments and showed that treating Populus saplings with inorganic nitrogen resulted in a delay in senescence. In addition, by using precise delivery of solutes into the xylem stream of Populus trees in their natural environment, we found that delay of autumn senescence was dependent on the form of N administered: inorganic N ((Formula presented.)) delayed senescence, but amino acids (Arg, Glu, Gln, and Leu) did not. Metabolite profiling of leaves showed that the levels of tricarboxylic acids, arginine catabolites (ammonium, ornithine), glycine, glycine-serine ratio and overall carbon-to-nitrogen (C/N) ratio were affected differently by the way of applying NO3− and Arg treatments. In addition, the onset of senescence did not coincide with soluble sugar accumulation in control trees or in any of the treatments. We propose that different regulation of C and N status through direct molecular signaling of NO3− and/or different allocation of N between tree parts depending on N forms could account for the contrasting effects of NO3− and tested here amino acids (Arg, Glu, Gln, and Leu) on autumn senescence.

Place, publisher, year, edition, pages
John Wiley & Sons, 2022
National Category
Botany
Identifiers
urn:nbn:se:umu:diva-203158 (URN)10.1111/ppl.13690 (DOI)000798701400001 ()35460591 (PubMedID)2-s2.0-85132885123 (Scopus ID)
Funder
Swedish Research CouncilSwedish Research Council FormasKnut and Alice Wallenberg FoundationVinnova
Available from: 2023-01-16 Created: 2023-01-16 Last updated: 2023-01-16Bibliographically approved
Boussardon, C., Bag, P., Juvany, M., Šimura, J., Ljung, K., Jansson, S. & Keech, O. (2022). The RPN12a proteasome subunit is essential for the multiple hormonal homeostasis controlling the progression of leaf senescence. Communications Biology, 5(1), Article ID 1043.
Open this publication in new window or tab >>The RPN12a proteasome subunit is essential for the multiple hormonal homeostasis controlling the progression of leaf senescence
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2022 (English)In: Communications Biology, E-ISSN 2399-3642, Vol. 5, no 1, article id 1043Article in journal (Refereed) Published
Abstract [en]

The 26S proteasome is a conserved multi-subunit machinery in eukaryotes. It selectively degrades ubiquitinated proteins, which in turn provides an efficient molecular mechanism to regulate numerous cellular functions and developmental processes. Here, we studied a new loss-of-function allele of RPN12a, a plant ortholog of the yeast and human structural component of the 19S proteasome RPN12. Combining a set of biochemical and molecular approaches, we confirmed that a rpn12a knock-out had exacerbated 20S and impaired 26S activities. The altered proteasomal activity led to a pleiotropic phenotype affecting both the vegetative growth and reproductive phase of the plant, including a striking repression of leaf senescence associate cell-death. Further investigation demonstrated that RPN12a is involved in the regulation of several conjugates associated with the auxin, cytokinin, ethylene and jasmonic acid homeostasis. Such enhanced aptitude of plant cells for survival in rpn12a contrasts with reports on animals, where 26S proteasome mutants generally show an accelerated cell death phenotype.

Place, publisher, year, edition, pages
Nature Publishing Group, 2022
National Category
Botany Biochemistry Molecular Biology
Identifiers
urn:nbn:se:umu:diva-200406 (URN)10.1038/s42003-022-03998-2 (DOI)000862402500001 ()36180574 (PubMedID)2-s2.0-85139221413 (Scopus ID)
Funder
The Kempe FoundationsCarl Tryggers foundation , CTS2018-193Swedish Foundation for Strategic Research, FFF20-0008Knut and Alice Wallenberg FoundationVinnova
Available from: 2022-10-21 Created: 2022-10-21 Last updated: 2025-02-20Bibliographically approved
Bag, P., Lihavainen, J., Delhomme, N., Riquelme, T., Robinson, K. M. & Jansson, S. (2021). An atlas of the Norway spruce needle seasonal transcriptome. The Plant Journal, 108(6), 1815-1829
Open this publication in new window or tab >>An atlas of the Norway spruce needle seasonal transcriptome
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2021 (English)In: The Plant Journal, ISSN 0960-7412, E-ISSN 1365-313X, Vol. 108, no 6, p. 1815-1829Article in journal (Refereed) Published
Abstract [en]

Boreal conifers possess a tremendous ability to survive and remain evergreen during harsh winter conditions and resume growth during summer. This is enabled by coordinated regulation of major cellular functions at the level of gene expression, metabolism, and physiology. Here we present a comprehensive characterization of the annual changes in the global transcriptome of Norway spruce (Picea abies) needles as a resource to understand needle development and acclimation processes throughout the year. In young, growing needles (May 15 until June 30), cell walls, organelles, etc., were formed, and this developmental program heavily influenced the transcriptome, explained by over-represented Gene Ontology (GO) categories. Later changes in gene expression were smaller but four phases were recognized: summer (July–August), autumn (September–October), winter (November–February), and spring (March–April), where over-represented GO categories demonstrated how the needles acclimated to the various seasons. Changes in the seasonal global transcriptome profile were accompanied by differential expression of members of the major transcription factor families. We present a tentative model of how cellular activities are regulated over the year in needles of Norway spruce, which demonstrates the value of mining this dataset, accessible in ConGenIE together with advanced visualization tools.

Place, publisher, year, edition, pages
John Wiley & Sons, 2021
Keywords
conifers, Norway spruce, resource, seasonal adaptation, transcriptomics
National Category
Botany
Identifiers
urn:nbn:se:umu:diva-188962 (URN)10.1111/tpj.15530 (DOI)000709512700001 ()34624161 (PubMedID)2-s2.0-85117463119 (Scopus ID)
Funder
EU, Horizon 2020, 675006VinnovaSwedish Research Council FormasKnut and Alice Wallenberg FoundationSwedish Research Council, 2018‐05973The Kempe Foundations
Available from: 2021-10-28 Created: 2021-10-28 Last updated: 2024-07-02Bibliographically approved
Fataftah, N., Bag, P., André, D., Lihavainen, J., Zhang, B., Ingvarsson, P. K., . . . Jansson, S. (2021). GIGANTEA influences leaf senescence in trees in two different ways. Plant Physiology, 187(4), 2435-2450
Open this publication in new window or tab >>GIGANTEA influences leaf senescence in trees in two different ways
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2021 (English)In: Plant Physiology, ISSN 0032-0889, E-ISSN 1532-2548, Vol. 187, no 4, p. 2435-2450Article in journal (Refereed) Published
Abstract [en]

GIGANTEA (GI) genes have a central role in plant development and influence several processes. Hybrid aspen T89 (Populus tremula x tremuloides) trees with low GI expression engineered through RNAi show severely compromised growth. To study the effect of reduced GI expression on leaf traits with special emphasis on leaf senescence, we grafted GI-RNAi scions onto wild-type rootstocks and successfully restored growth of the scions. The RNAi line had a distorted leaf shape and reduced photosynthesis, probably caused by modulation of phloem or stomatal function, increased starch accumulation, a higher carbon-to-nitrogen ratio, and reduced capacity to withstand moderate light stress. GI-RNAi also induced senescence under long day (LD) and moderate light conditions. Furthermore, the GI-RNAi lines were affected in their capacity to respond to “autumn environmental cues” inducing senescence, a type of leaf senescence that has physiological and biochemical characteristics that differ from those of senescence induced directly by stress under LD conditions. Overexpression of GI delayed senescence under simulated autumn conditions. The two different effects on leaf senescence under LD or simulated autumn conditions were not affected by the expression of FLOWERING LOCUS T. GI expression regulated leaf senescence locally-the phenotype followed the genotype of the branch, independent of its position on the tree-and trees with modified gene expression were affected in a similar way when grown in the field as under controlled conditions. Taken together, GI plays a central role in sensing environmental changes during autumn and determining the appropriate timing for leaf senescence in Populus.

Place, publisher, year, edition, pages
Oxford University Press, 2021
National Category
Botany Plant Biotechnology
Identifiers
urn:nbn:se:umu:diva-190823 (URN)10.1093/plphys/kiab439 (DOI)000733403700044 ()2-s2.0-85121117394 (Scopus ID)
Funder
VinnovaSwedish Research Council FormasKnut and Alice Wallenberg FoundationSwedish Research CouncilEU, Horizon 2020, 675006
Available from: 2021-12-29 Created: 2021-12-29 Last updated: 2023-09-05Bibliographically approved
Bag, P. (2021). Light harvesting in fluctuating environments: Evolution and function of antenna proteins across photosynthetic lineage. PLANTS, 10(6), Article ID 1184.
Open this publication in new window or tab >>Light harvesting in fluctuating environments: Evolution and function of antenna proteins across photosynthetic lineage
2021 (English)In: PLANTS, E-ISSN 2223-7747, Vol. 10, no 6, article id 1184Article in journal (Refereed) Published
Abstract [en]

Photosynthesis is the major natural process that can harvest and harness solar energy into chemical energy. Photosynthesis is performed by a vast number of organisms from single cellular bacteria to higher plants and to make the process efficient, all photosynthetic organisms possess a special type of pigment protein complex(es) that is (are) capable of trapping light energy, known as photosynthetic light-harvesting antennae. From an evolutionary point of view, simpler (unicellular) organisms typically have a simple antenna, whereas higher plants possess complex antenna systems. The higher complexity of the antenna systems provides efficient fine tuning of photosynthesis. This relationship between the complexity of the antenna and the increasing complexity of the organism is mainly related to the remarkable acclimation capability of complex organisms under fluctuating environmental conditions. These antenna complexes not only harvest light, but also provide photoprotection under fluctuating light conditions. In this review, the evolution, structure, and function of different antenna complexes, from single cellular organisms to higher plants, are discussed in the context of the ability to acclimate and adapt to cope under fluctuating environmental conditions.

Place, publisher, year, edition, pages
MDPI, 2021
Keywords
Angiosperms, Cyanobacteria, Evolution, Gymnosperms, Light-harvesting complexes, Photoprotection, Photosynthesis, Phycobilisomes
National Category
Botany Biochemistry Molecular Biology
Identifiers
urn:nbn:se:umu:diva-184682 (URN)10.3390/plants10061184 (DOI)000666692800001 ()2-s2.0-85107466248 (Scopus ID)
Available from: 2021-06-17 Created: 2021-06-17 Last updated: 2025-02-20Bibliographically approved
Organisations
Identifiers
ORCID iD: ORCID iD iconorcid.org/0000-0003-3858-4606

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