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Publications for Min Chen 2020 of five hydroxymethyl chlorophyll a derivatives chemically Kato, K., Shinoda, T., Nagao, R., Akimoto, S., Suzuki, T., derived from chlorophyll b or chlorophyll f. Photosynthesis Dohmae, N., Chen, M., Allakhverdiev, S., Shen, J., Akita, F., et Research, 140(1), 115-127. <a al (2020). Structural basis for the adaptation and function of href="http://dx.doi.org/10.1007/s11120-018-00611-8">[More chlorophyll f in photosystem I. Nature Communications, 11(1), Information]</a> 1-10. <a href="http://dx.doi.org/10.1038/s41467-019-13898- Zhang, Z., Li, Z., Yin, Y., Li, Y., Jia, Y., Chen, M., Qiu, B. 5">[More Information]</a> (2019). Widespread occurrence and unexpected diversity of red- 2019 shifted chlorophyll producing cyanobacteria in humid subtropical forest ecosystems. Environmental Microbiology, Chen, M. (2019). Chlorophylls d and f: Synthesis, occurrence, 21(4), 1497-1510. <a href="http://dx.doi.org/10.1111/1462- light-harvesting, and pigment organization in chlorophyll- 2920.14582">[More Information]</a> binding protein complexes. In Bernhard Grimm (Eds.), Metabolism, Structure and Function of Plant Tetrapyrroles: 2018 Introduction, Microbial and Eukaryotic Chlorophyll Synthesis Li, Y., Vella, N., Chen, M. (2018). Characterization of isolated and Catabolism, (pp. 121-139). London: Academic Press. <a photosystem I from Halomicronema hongdechloris, a href="http://dx.doi.org/10.1016/bs.abr.2019.03.006">[More chlorophyll f-producing cyanobacterium. Photosynthetica, Information]</a> 56(1), 306-315. <a href="http://dx.doi.org/10.1007/s11099-018- Hernandez-Prieto, M., Foster, C., Watson-Lazowski, A., 0776-x">[More Information]</a> Ghannoum, O., Chen, M. (2019). Comparative analysis of Hernandez-Prieto, M., Li, Y., Postier, B., Blankenship, R., thylakoid protein complexes in the mesophyll and bundle Chen, M. (2018). Far-red light promotes biofilm formation in sheath cells from C3, C4 and C3�C4 Paniceae grasses. the cyanobacterium Acaryochloris marina. Environmental Physiologia Plantarum, 166(1), 134-147. <a Microbiology, 20(2), 535-545. <a href="http://dx.doi.org/10.1111/ppl.12956">[More href="http://dx.doi.org/10.1111/1462-2920.13961">[More Information]</a> Information]</a> Fisher, A., Wangpraseurt, D., Larkum, A., Johnson, M., Kuhl, Song, W., Zang, S., Li, Z., Dai, G., Liu, K., Chen, M., Qiu, B. M., Chen, M., Wong, H., Burns, B. (2019). Correlation of bio- (2018). Sycrp2 Is Essential for Twitching Motility in the optical properties with photosynthetic pigment and Cyanobacterium Synechocystis sp. Strain PCC 6803. Journal of microorganism distribution in microbial mats from Hamelin Bacteriology, 200(21), 1-13. <a Pool, Australia. FEM Microbiology Ecology, 95(1), 1-13. <a href="http://dx.doi.org/10.1128/JB.00436-18">[More href="http://dx.doi.org/10.1093/femsec/fiy219">[More Information]</a> Information]</a> Li, Z., Yin, Y., Zhang, L., Zhang, Z., Dai, G., Chen, M., Qiu, B. Chen, M., Hernandez-Prieto, M., Loughlin, P., Li, Y., Willows, (2018). The identification of IsiA proteins binding chlorophyll d R. (2019). Genome and proteome of the chlorophyll f- in the cyanobacterium Acaryochloris marina. Photosynthesis producing cyanobacterium Halomicronema hongdechloris: Research, 135(1-3), 165-175. <a Adaptative proteomic shifts under different light conditions. href="http://dx.doi.org/10.1007/s11120-017-0379-6">[More BMC Genomics, 20(1), 1-20. <a Information]</a> href="http://dx.doi.org/10.1186/s12864-019-5587-3">[More Information]</a> Shang, J., Zhang, Z., Yin, X., Chen, M., Hao, F., Wang, K., Feng, J., Xu, H., Yin, Y., Tang, H., et al (2018). UV-B induced Shang, J., Chen, M., Hou, S., Li, T., Yang, Y., Li, Q., Jiang, H., biosynthesis of a novel sunscreen compound in solar radiation Dai, G., Zhang, Z., Hess, W., et al (2019). Genomic and and desiccation tolerant cyanobacteria. Environmental transcriptomic insights into the survival of the subaerial Microbiology, 20(1), 200-213. <a cyanobacterium Nostoc flagelliforme in arid and exposed href="http://dx.doi.org/10.1111/1462-2920.13972">[More habitats. Environmental Microbiology, 21(2), 845-863. <a Information]</a> href="http://dx.doi.org/10.1111/1462-2920.14521">[More Information]</a> 2017 Yang, Y., Yin, Y., Li, Z., Huang, D., Shang, J., Chen, M., Qiu, Zang, S., Jiang, H., Song, W., Chen, M., Qiu, B. (2017). B. (2019). Orange and red carotenoid proteins are involved in Characterization of the sulfur-formation (suf) genes in the adaptation of the terrestrial cyanobacterium Nostoc Synechocystis sp. PCC 6803 under photoautotrophic and flagelliforme to desiccation. Photosynthesis Research, 140(1), heterotrophic growth conditions. Planta, 246(5), 927-938. <a 103-113. <a href="http://dx.doi.org/10.1007/s11120-019-00629- href="http://dx.doi.org/10.1007/s00425-017-2738-0">[More 6">[More Information]</a> Information]</a> Schmitt, F., Campbell, Z., Bui, M., Huls, A., Tomo, T., Chen, Baker, J., Riester, C., Skinner, B., Newell, A., Swingley, W., M., Maksimov, E., Allakhverdiev, S., Friedrich, T. (2019). Madigan, M., Jung, D., Asao, M., Chen, M., Loughlin, P., Pan, Photosynthesis supported by a chlorophyll f-dependent, entropy- H., Lin, Y., Li, Y., et al (2017). Genome Sequence of driven uphill energy transfer in Halomicronema hongdechloris Rhodoferax antarcticus ANT.BRT; A Psychrophilic Purple cells adapted to far-red light. Photosynthesis Research, 139(1- Nonsulfur Bacterium from an Antarctic Microbial Mat. Mar), 185-201. <a href="http://dx.doi.org/10.1007/s11120-018- Microorganisms, 5(1), 1-16. <a 0556-2">[More Information]</a> href="http://dx.doi.org/10.3390/microorganisms5010008">[Mor Sawicki, A., Willows, R., Chen, M. (2019). Spectral signatures e Information]</a> Majumder, E., Wolf, B., Liu, H., Berg, R., Timlin, J., Chen, M., Blankenship, R. (2017). Subcellular pigment distribution is Chen, M. (2014). Chlorophyll Modifications and Their Spectral altered under far-red light acclimation in cyanobacteria that Extension in Oxygenic Photosynthesis. Annual Review of contain chlorophyll f. Photosynthesis Research, 134(2), 183- Biochemistry, 83, 317-340. <a 192. <a href="http://dx.doi.org/10.1007/s11120-017-0428- href="http://dx.doi.org/10.1146/annurev-biochem-072711- 1">[More Information]</a> 162943">[More Information]</a> Garg, H., Loughlin, P., Willows, R., Chen, M. (2017). The C21- Paul, R., Jinkerson, R., Buss, K., Steel, J., Mohr, R., Hess, W., formyl group in chlorophyll f originates from molecular Chen, M., Fromme, P. (2014). Draft Genome Sequence of the oxygen. Journal of Biological Chemistry, 292(47), 19279- Filamentous Cyanobacterium Leptolyngbya sp. Strain Heron 19289. <a Island J, Exhibiting Chromatic Acclimation. Genome href="http://dx.doi.org/10.1074/jbc.M117.814756">[More Announcements, 2(1), 1-2. <a Information]</a> href="http://dx.doi.org/10.1128/genomeA.01166-13">[More Information]</a> Hernandez-Prieto, M., Lin, Y., Chen, M. (2017). The Complex Transcriptional Response of Acaryochloris marina to Different Tomo, T., Shinoda, T., Chen, M., Allakhverdiev, S., Akimoto, Oxygen Levels. G3: Genes, Genomes, Genetics, 7, 517-532. <a S. (2014). Energy transfer processes in chlorophyll f-containing href="http://dx.doi.org/10.1534/g3.116.036855">[More cyanobacteria using time-resolved fluorescence spectroscopy on Information]</a> intact cells. Biochimica et Biophysica Acta, 1837 (9), 1484- 1489. <a 2016 href="http://dx.doi.org/10.1016/j.bbabio.2014.04.009">[More Information]</a> Brazao, S., Chen, M., Murphy, R., Simpson, S., Coleman, R. (2016). A method for growing a monospecific epilithic Niedzwiedzki, D., Liu, H., Chen, M., Blankenship, R. (2014). cyanobacterial biofilm for use in marine ecological Excited state properties of chlorophyll f in organic solvents at experiments. Journal of Experimental Marine Biology and ambient and cryogenic temperatures. Photosynthesis Research, Ecology, 480, 17-25. <a 121(1), 25-34. <a href="http://dx.doi.org/10.1007/s11120-014- href="http://dx.doi.org/10.1016/j.jembe.2016.03.013">[More 9981-z">[More Information]</a> Information]</a> Loughlin, P., Willows, R., Chen, M. (2014). In vitro conversion Li, Y., Lin, Y., Garvey, C., Birch, D., Corkery, R., Loughlin, P., of vinyl to formyl groups in naturally occurring chlorophylls. Scheer, H., Willows, R., Chen, M. (2016). Characterization of Scientific Reports, 4, 1-9. <a red-shifted phycobilisomes isolated from the chlorophyll f- href="http://dx.doi.org/10.1038/srep06069">[More containing cyanobacterium Halomicronema hongdechloris. Information]</a> Biochimica et Biophysica Acta, 1857 (1), 107-114. <a Foster, C., Portman, N., Chen, M., Slapeta, J. (2014). Increased href="http://dx.doi.org/10.1016/j.bbabio.2015.10.009">[More growth and pigment content of Chromera velia in mixotrophic Information]</a> culture. FEM Microbiology Ecology, 88(1), 121-128. <a Chen, M. (2016). Martin F. Homann-Marriott (ed.): The href="http://dx.doi.org/10.1111/1574-6941.12275">[More structural basis Information]</a> of biological energy generation. Photosynthesis Research, Li, Y., Lin, Y., Loughlin, P., Chen, M. (2014). Optimization 128(1), 103-105. <a href="http://dx.doi.org/10.1007/s11120- and effects of different culture conditions on growth of 015-0204-z">[More Information]</a> Halomicronema hongdechloris - a filamentous cyanobacterium Loughlin, P., Duxbury, Z., Mukasa-Mugerwa, T., Smith, P., containing chlorophyll f. Frontiers in Plant Science, 5(FEB), 1- Willows, R., Chen, M. (2016). Spectral properties of 12. <a href="http://dx.doi.org/10.3389/fpls.2014.00067">[More bacteriophytochrome AM1_5894 in the chlorophyll d- Information]</a> containing cyanobacterium Acaryochloris marina. Scientific Reports, 6, 1-12. <a 2013 href="http://dx.doi.org/10.1038/srep27547">[More Loughlin, P., Lin, Y., Chen, M. (2013). Chlorophyll d and Information]</a> Acaryochloris marina: current status. Photosynthesis Research, 2015 116(2-3), 277-293. <a href="http://dx.doi.org/10.1007/s11120- 013-9829-y">[More Information]</a> Akimoto, S., Shinoda, T., Chen, M., Allakhverdiev, S., Tomo, Chen, M., Scheer, H. (2013). Extending the limits of natural T.
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  • Far-Red Light Acclimation for Improved Mass Cultivation of Cyanobacteria

    Far-Red Light Acclimation for Improved Mass Cultivation of Cyanobacteria

    H OH metabolites OH Article Far-Red Light Acclimation for Improved Mass Cultivation of Cyanobacteria Alla Silkina 1 , Bethan Kultschar 2 and Carole A. Llewellyn 2,* 1 Centre for Sustainable Aquatic Research (CSAR), Bioscience department, College of Science, Swansea University, Singleton Park, Swansea SA2 8PP, UK 2 Department of Biosciences, College of Science, Swansea University, Singleton Park, Swansea SA2 8PP, UK * Correspondence: [email protected] Received: 1 August 2019; Accepted: 15 August 2019; Published: 19 August 2019 Abstract: Improving mass cultivation of cyanobacteria is a goal for industrial biotechnology. In this study, the mass cultivation of the thermophilic cyanobacterium Chlorogloeopsis fritschii was assessed for biomass production under light-emitting diode white light (LEDWL), far-red light (FRL), and combined white light and far-red light (WLFRL) adaptation. The induction of chl f was confirmed at 24 h after the transfer of culture from LEDWL to FRL. Using combined light (WLFRL), chl f, a, and d, maintained the same level of concentration in comparison to FRL conditions. However, phycocyanin and xanthophylls (echinone, caloxanthin, myxoxanthin, nostoxanthin) concentration increased 2.7–4.7 times compared to LEDWL conditions. The productivity of culture was double under WLFRL compared with LEDWL conditions. No significant changes in lipid, protein, and carbohydrate concentrations were found in the two different light conditions. The results are important for informing on optimum biomass cultivation of this species for biomass production and bioactive product development. Keywords: cyanobacteria; chromatic adaptation; LED; far-red light; growth; photosynthesis; mass cultivation; pigments; Chlorogloeopsis 1. Introduction Cyanobacteria are photosynthetic prokaryotes that are increasingly explored for use in industrial biotechnology.
  • Cold-Induced Photoinhibition, Pigment Chemistry, Growth and Nutrition of Eucalyptus Nitens and E

    Cold-Induced Photoinhibition, Pigment Chemistry, Growth and Nutrition of Eucalyptus Nitens and E

    Cold-induced photoinhibition, pigment chemistry, growth and nutrition of Eucalyptus nitens and E. globulus seedlings during establishment Dugald C. Close Submitted in fulfilment of the requirements for the degree of Doctor of Philosophy Schools of Agricultural and Plant Science .and CRC for Sustainable Production Forestry University of Tasmania Declarations This thesis contains no material which has been accepted for a degree or diploma by the University of Tasmania or any other institution. To the best of my knowledge and belief this thesis contains no material previously published or written by another person except where due acknowledgement is made in the text of the thesis. Dugald C. Close This thesis may be made available for loan and limited copying in accordance with the Copyright Act 1968. Dugald C. Close Abstract Australia is aiming to treble plantation wood production by 2020. Eucalyptus globulus Labill. and E. nitens (Deane and Maidem) Maiden are the predominant plantation species in southern Australia. This thesis describes physiological strategies employed by these species in response to cold-induced photoinhibition during seedling establishment. A series of experiments was conducted on seedlings pre- hardened in the nursery. Their physiological and growth responses after planting in the field was investigated. A field trial was established at 350 m asl in early spring 1997. Severe cold-induced photoinhibition caused photodamage which restricted growth of non-hardened E. globulus. Artificial shading alleviated cold-induced photoinhibition and photodamage in both E. globulus and E. nitens, and increased growth in E. globulus. Before planting, nutrient-starved E. nitens were photoinhibited and had high anthocyanin levels.
  • Excited State Frequencies of Chlorophyll F and Chlorophyll a and Evaluation of Displacement Through Franck-Condon Progression Calculations

    Excited State Frequencies of Chlorophyll F and Chlorophyll a and Evaluation of Displacement Through Franck-Condon Progression Calculations

    molecules Article Excited State Frequencies of Chlorophyll f and Chlorophyll a and Evaluation of Displacement through Franck-Condon Progression Calculations Noura Zamzam and Jasper J. van Thor * Department of Life Sciences, Molecular Biophysics, Imperial College London, London SW7 2AZ, UK; [email protected] * Correspondence: [email protected]; Tel.: +44-(0)20-7594-5071 Academic Editor: Chong Fang Received: 16 February 2019; Accepted: 2 April 2019; Published: 4 April 2019 Abstract: We present ground and excited state frequency calculations of the recently discovered extremely red-shifted chlorophyll f. We discuss the experimentally available vibrational mode assignments of chlorophyll f and chlorophyll a which are characterised by particularly large downshifts of 131-keto mode in the excited state. The accuracy of excited state frequencies and their displacements are evaluated by the construction of Franck–Condon (FC) and Herzberg–Teller (HT) progressions at the CAM-B3LYP/6-31G(d) level. Results show that while CAM-B3LYP results are improved relative to B3LYP calculations, the displacements and downshifts of high-frequency modes are underestimated still, and that the progressions calculated for low temperature are dominated by low-frequency modes rather than fingerprint modes that are Resonant Raman active. Keywords: vibrational frequencies; chlorophyll a; chlorophyll f; excited state; density functional theory; B3LYP; CAM-B3LYP; Franck–Condon 1. Introduction Chlorophylls found in photosynthetic organisms are responsible for light harvesting in the antenna complexes, and the subsequent transfer of excitation energy to photosynthetic reaction centres with almost 100% quantum efficiency. In the reaction centres, specific chlorophylls act as electron transfer cofactors and are involved in the initial charge separation processes [1].