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Journal articles on the topic 'Chlamydomona reinhardtii'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Craig, Rory J., Ahmed R. Hasan, Rob W. Ness, and Peter D. Keightley. "Comparative genomics of Chlamydomonas." Plant Cell 33, no. 4 (2021): 1016–41. http://dx.doi.org/10.1093/plcell/koab026.

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Abstract Despite its role as a reference organism in the plant sciences, the green alga Chlamydomonas reinhardtii entirely lacks genomic resources from closely related species. We present highly contiguous and well-annotated genome assemblies for three unicellular C. reinhardtii relatives: Chlamydomonas incerta, Chlamydomonas schloesseri, and the more distantly related Edaphochlamys debaryana. The three Chlamydomonas genomes are highly syntenous with similar gene contents, although the 129.2 Mb C. incerta and 130.2 Mb C. schloesseri assemblies are more repeat-rich than the 111.1 Mb C. reinhard

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2

Podstavková, Svetlana, Daniel Vlček, Eva Miadoková, and Andrea Slivková. "The localization of Chlamydomonas reinhardtii repair genes." Algological Studies/Archiv für Hydrobiologie, Supplement Volumes 82 (November 21, 1996): 97–102. http://dx.doi.org/10.1127/algol_stud/82/1996/97.

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3

Stepanov, S. S. "Stimulation of accumulation of lipid bodies in Chlamydomonas reinhardtii cells." Studia Biologica 10, no. 3–4 (2016): 165–68. http://dx.doi.org/10.30970/sbi.1003.482.

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4

Lechtreck, Karl F. "Chlamydomonas reinhardtii as a model for flagellar assembly." Perspectives in Phycology 1, no. 1 (2014): 41–51. http://dx.doi.org/10.1127/2198-011x/2014/0006.

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5

Vlčková, Viera, Svetlana Podstavková, Miroslava Slaninová, Eva Miadoková, and Daniel Vlček. "The green alga Chlamydomonas reinhardtii: bioactivator of nitrosoamines." Algological Studies/Archiv für Hydrobiologie, Supplement Volumes 100 (December 20, 2000): 181–93. http://dx.doi.org/10.1127/algol_stud/100/2000/181.

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6

Huong, Nguyen Minh, Ha Thi Thu, Nguyen Thi Hoa, et al. "Creation of recombinant Chlamydomonas reinhardtii strains expressing codon optimized vp28 gene from white spot symdrome virus." TAP CHI SINH HOC 40, no. 1 (2018): 92–99. http://dx.doi.org/10.15625/0866-7160/v40n1.10988.

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White spot syndrome virus (WSSV) is the leading cause of shrimp mortality in farms all over the world. In Vietnam, for the last five to ten years, WSSV has always been among the top causes of diseases and loss in our shrimp aquaculture. VP28 and VP26 are two capsid proteins of WSSV that commonly used as biomarkers for diagnosis and target antigens for vaccine against WSSV. Recombinant VP28 (rVP28) has been studied and expressed in various expression systems including E. coli, yeast and baculovirus. rVP28 expressed in these systems showed effective protection against WSSV in shrimps, though the

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7

Husic, H. David. "Extracellular carbonic anhydrase of Chlamydomonas reinhardtii: localization, structural properties, and catalytic properties." Canadian Journal of Botany 69, no. 5 (1991): 1079–87. http://dx.doi.org/10.1139/b91-138.

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In the unicellular green alga Chlamydomonas reinhardtii, a form of the enzyme carbonic anhydrase that is localized outside of the plasma membrane is an inducible component of a system that is involved in inorganic carbon acquisition and concentration from the growth medium. This article contains a review and analysis of the current literature regarding the extracellular carbonic anhydrase from Chlamydomonas reinhardtii and presents some new studies on its extracellular localization, physiological role in inorganic carbon acquisition, and some of the structural and catalytic properties of the e

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8

Stauber, Einar J., and Michael Hippler. "Chlamydomonas reinhardtii proteomics." Plant Physiology and Biochemistry 42, no. 12 (2004): 989–1001. http://dx.doi.org/10.1016/j.plaphy.2004.09.008.

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9

Roesler, Keith R., and William L. Ogren. "Chlamydomonas reinhardtii Phosphoribulokinase." Plant Physiology 93, no. 1 (1990): 188–93. http://dx.doi.org/10.1104/pp.93.1.188.

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10

Koblenz, Bettina, and Karl-Ferdinand Lechtreck. "The NIT1 Promoter Allows Inducible and Reversible Silencing of Centrin in Chlamydomonas reinhardtii." Eukaryotic Cell 4, no. 11 (2005): 1959–62. http://dx.doi.org/10.1128/ec.4.11.1959-1962.2005.

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ABSTRACT An inverted repeat corresponding to parts of the centrin gene of Chlamydomonas reinhardtii was placed downstream of the NIT1 promoter, which is induced by ammonium starvation. After induction, transformants developed centrin deficiency as assayed by immunofluorescence, Western blotting, and Northern blotting. The effect was reversible, demonstrating that the NIT1 promoter allowed controlled RNA interference in Chlamydomonas reinhardtii.

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11

Stepanov, S. S. "Accumulation of neutral lipids in the cells of Chlamydomonas reinhardtii under stress conditions." Fiziologia rastenij i genetika 48, no. 5 (2016): 401–15. http://dx.doi.org/10.15407/frg2016.05.401.

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12

Dimitrova, Maria, Evgeniya Dimova, Zhana Mitrovska, Veneta Kapchina-Toteva, and Stephka Chankova. "Testing of polluted soil samples for genotoxic potential using Chlamydomonas reinhardtii." Algological Studies 123 (May 1, 2007): 111–21. http://dx.doi.org/10.1127/1864-1318/2007/0123-0111.

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13

Brown, L. E., S. L. Sprecher, and L. R. Keller. "Introduction of exogenous DNA into Chlamydomonas reinhardtii by electroporation." Molecular and Cellular Biology 11, no. 4 (1991): 2328–32. http://dx.doi.org/10.1128/mcb.11.4.2328.

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The fate of exogenous DNA introduced into Chlamydomonas reinhardtii by electroporation was analyzed. With single and double electrical pulses, plasmids as large as 14 kb were introduced into cells with and without intact cell walls. Within hours after introduction, exogenous plasmid DNA was associated with nuclei isolated from cells; several weeks after introduction, exogenous DNA was stably integrated into the Chlamydomonas genome. These studies establish electroporation as a method for introducing DNA, and potentially other molecules, into C. reinhardtii.

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14

Brown, L. E., S. L. Sprecher, and L. R. Keller. "Introduction of exogenous DNA into Chlamydomonas reinhardtii by electroporation." Molecular and Cellular Biology 11, no. 4 (1991): 2328–32. http://dx.doi.org/10.1128/mcb.11.4.2328-2332.1991.

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The fate of exogenous DNA introduced into Chlamydomonas reinhardtii by electroporation was analyzed. With single and double electrical pulses, plasmids as large as 14 kb were introduced into cells with and without intact cell walls. Within hours after introduction, exogenous plasmid DNA was associated with nuclei isolated from cells; several weeks after introduction, exogenous DNA was stably integrated into the Chlamydomonas genome. These studies establish electroporation as a method for introducing DNA, and potentially other molecules, into C. reinhardtii.

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15

Hou, Qintang, Shi Qiu, Qiong Liu, Jing Tian, Zhangli Hu, and Jiazuan Ni. "Selenoprotein-Transgenic Chlamydomonas reinhardtii." Nutrients 5, no. 3 (2013): 624–36. http://dx.doi.org/10.3390/nu5030624.

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16

Matagne, R. F., C. Remacle, and M. Dinant. "Cytoduction in Chlamydomonas reinhardtii." Proceedings of the National Academy of Sciences 88, no. 16 (1991): 7447–50. http://dx.doi.org/10.1073/pnas.88.16.7447.

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17

Hamilton, Bradford S., Kazuo Nakamura, and Daniel A. K. Roncari. "Accumulation of starch in Chlamydomonas reinhardtii flagellar mutants." Biochemistry and Cell Biology 70, no. 3-4 (1992): 255–58. http://dx.doi.org/10.1139/o92-039.

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Paralyzed flagellar mutants pf-1, pf-2, pf-7, and pf-18 of the green alga Chlamydomonas reinhardtii (Dangeard) were shown to store a significantly greater amount of starch than the motile wild type 137c+. The increase in starch storage was significant relative to protein, chlorophyll, and cell number. Analysis of average cell size revealed that the paralyzed mutants were larger than the wild type. This increase in storage molecule accumulation supports an inverse relationship between chemical energy storage and energy utilization for biomechanical/motile cellular functions. Chlamydomonas reinh

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18

Goto, K., and C. H. Johnson. "Is the cell division cycle gated by a circadian clock? The case of Chlamydomonas reinhardtii." Journal of Cell Biology 129, no. 4 (1995): 1061–69. http://dx.doi.org/10.1083/jcb.129.4.1061.

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Circadian oscillators are known to regulate the timing of cell division in many organisms. In the case of Chlamydomonas reinhardtii, however, this conclusion has been challenged by several investigators. We have reexamined this issue and find that the division behavior of Chlamydomonas meets all the criteria for circadian rhythmicity: persistence of a cell division rhythm (a) with a period of approximately 24 h under free-running conditions, (b) that is temperature compensated, and (c) which can entrain to light/dark signals. In addition, a mutation that lengthens the circadian period of the p

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19

Jeong, Won-Joong, Jang-Ryol Liu, and Heriberto Cerutti. "Genetic Transformation of Chlamydomonas reinhardtii with the RNAi Suppressor p19 Gene of Tombus Virus." Journal of Plant Biotechnology 34, no. 4 (2007): 307–12. http://dx.doi.org/10.5010/jpb.2007.34.4.307.

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20

Kselíková, Veronika, Vilém Zachleder, and Kateřina Bišová. "To Divide or Not to Divide? How Deuterium Affects Growth and Division of Chlamydomonas reinhardtii." Biomolecules 11, no. 6 (2021): 861. http://dx.doi.org/10.3390/biom11060861.

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Extensive in vivo replacement of hydrogen by deuterium, a stable isotope of hydrogen, induces a distinct stress response, reduces cell growth and impairs cell division in various organisms. Microalgae, including Chlamydomonas reinhardtii, a well-established model organism in cell cycle studies, are no exception. Chlamydomonas reinhardtii, a green unicellular alga of the Chlorophyceae class, divides by multiple fission, grows autotrophically and can be synchronized by alternating light/dark regimes; this makes it a model of first choice to discriminate the effect of deuterium on growth and/or d

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21

Volgusheva, Alena, Galina Kukarskikh, Tatyana Krendeleva, Andrey Rubin, and Fikret Mamedov. "Hydrogen photoproduction in green algae Chlamydomonas reinhardtii under magnesium deprivation." RSC Advances 5, no. 8 (2015): 5633–37. http://dx.doi.org/10.1039/c4ra12710b.

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22

Miadoková, Eva, Svetlana Podstavková, and Daniel Vlček. "Caffeine effects on UV-mutability of repair-deficient strains of Chlamydomonas reinhardtii." Algological Studies/Archiv für Hydrobiologie, Supplement Volumes 79 (December 14, 1995): 109–17. http://dx.doi.org/10.1127/algol_stud/79/1995/109.

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23

Nakamura, Kazuo, Charles F. Landry, Christine A. Goertzen, and N. Wayne Ikebuchi. "Limited uptake as a mechanism for the nonrecoverability of arginine auxotrophs in Chlamydomonas eugametos." Canadian Journal of Botany 63, no. 5 (1985): 909–15. http://dx.doi.org/10.1139/b85-120.

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To address the problem of amino acid auxotroph scarcities in algae, an explanation was sought specifically for the nonrecoverability of arginine auxotrophs in the unicellular green alga Chlamydomonas eugametos. Chlamydomonas reinhardtii, in which the auxotroph has been recovered, was taken as a reference. In C. eugametos, unlike previously reported in C. reinhardtii, the use of selective media free of [Formula: see text] appeared not to affect the mutation spectrum. Arginine supported growth as the sole nitrogen source and canavanine sulfate inhibited growth, but both effects were less pronoun

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24

Hotter, Vivien, David Zopf, Hak Joong Kim, et al. "A polyyne toxin produced by an antagonistic bacterium blinds and lyses a Chlamydomonad alga." Proceedings of the National Academy of Sciences 118, no. 33 (2021): e2107695118. http://dx.doi.org/10.1073/pnas.2107695118.

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Algae are key contributors to global carbon fixation and form the basis of many food webs. In nature, their growth is often supported or suppressed by microorganisms. The bacterium Pseudomonas protegens Pf-5 arrests the growth of the green unicellular alga Chlamydomonas reinhardtii, deflagellates the alga by the cyclic lipopeptide orfamide A, and alters its morphology [P. Aiyar et al., Nat. Commun. 8, 1756 (2017)]. Using a combination of Raman microspectroscopy, genome mining, and mutational analysis, we discovered a polyyne toxin, protegencin, which is secreted by P. protegens, penetrates the

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25

Spalding, Martin H., Kyujung Van, Yingjun Wang, and Yoshiko Nakamura. "Acclimation of Chlamydomonas to changing carbon availability." Functional Plant Biology 29, no. 3 (2002): 221. http://dx.doi.org/10.1071/pp01182.

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Aquatic organisms, including Chlamydomonas reinhardtii, are faced with a variable supply of dissolved inorganic carbon (Ci). Accordingly, C. reinhardtii has the ability to acclimate to the changing Ci supply through a variety of responses, including induction of a CO2 concentrating mechanism (CCM) when Ci is limiting. The CCM uses active Ci uptake to accumulate a high internal concentration of bicarbonate, which is dehydrated by a specific thylakoid carbonic anhydrase to supply CO2, the substrate used in photosynthesis. In addition to the changes demonstrably related to the function of the CCM

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26

Tural, Baran, and James V. Moroney. "Regulation of the expression of photorespiratory genes inChlamydomonas reinhardtii." Canadian Journal of Botany 83, no. 7 (2005): 810–19. http://dx.doi.org/10.1139/b05-066.

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The regulation of the photorespiratory pathway in Chlamydomonas reinhardtii Dangeard during a shift from high- to low-CO2conditions was investigated. To this end, a set of C. reinhardtii cDNA sequences for known photorespiratory enzymes was assembled using the Chlamydomonas expressed sequence tag database and primary sequencing data. Expression data indicates that there is a rapid and coordinated induction of photorespiratory and CCM gene expression during a time course switch from high-CO2conditions (5% (v/v)) to low-CO2conditions (0.038% (v/v)). While the expression of photorespiratory and C

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27

Bertiaux-Lequoy, Eloïse, Philippe Hammel, Virginie Hamel, and Paul Guichard. "The RB530 antibody recognizes microtubules by immunofluorescence." Antibody Reports 2, no. 4 (2019): e65. http://dx.doi.org/10.24450/journals/abrep.2019.e65.

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28

Yogesha, M., Venkatramanan G. Rao, Elvis A. F. Martis, et al. "Structural features of FAP174, a MYCBP-1 orthologue from Chlamydomonas reinhardtii, revealed by computational and experimental analyses." RSC Advances 7, no. 81 (2017): 51391–402. http://dx.doi.org/10.1039/c7ra07836f.

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29

Kathir, Pushpa, Matthew LaVoie, William J. Brazelton, Nancy A. Haas, Paul A. Lefebvre, and Carolyn D. Silflow. "Molecular Map of the Chlamydomonas reinhardtii Nuclear Genome." Eukaryotic Cell 2, no. 2 (2003): 362–79. http://dx.doi.org/10.1128/ec.2.2.362-379.2003.

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ABSTRACT We have prepared a molecular map of the Chlamydomonas reinhardtii genome anchored to the genetic map. The map consists of 264 markers, including sequence-tagged sites (STS), scored by use of PCR and agarose gel electrophoresis, and restriction fragment length polymorphism markers, scored by use of Southern blot hybridization. All molecular markers tested map to one of the 17 known linkage groups of C. reinhardtii. The map covers approximately 1,000 centimorgans (cM). Any position on the C. reinhardtii genetic map is, on average, within 2 cM of a mapped molecular marker. This molecular

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30

Thomas, James E., Christine A. Goertzen, and Kazuo Nakamura. "Heterogeneity in endogenous amino acid pools of Chlamydomonas reinhardtii and C. eugametos." Canadian Journal of Botany 69, no. 6 (1991): 1194–98. http://dx.doi.org/10.1139/b91-153.

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Levels of endogenous amino acid pools were measured for two species of the unicellular green alga Chlamydomonas. In C. reinhardtii, opposite mating types, designated + and −, of strain 137c were examined. The soluble pool of glutamic acid was most abundant in strain 137c−. In strain 137c+ similar levels of this amino acid were present, and high levels of cystine were observed. A soluble pool for the amino acid methionine was not detected in either strain. In opposite mating types of C. eugametos (strain Nos. 9 and 10), a soluble pool of alanine was most abundant, whereas neither cystine nor me

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31

Chen, Zhenzhong, and Won Gu Lee. "A switching role of hard-uptake nanoparticles in microalgae cell electroporation." Analyst 144, no. 11 (2019): 3581–89. http://dx.doi.org/10.1039/c9an00314b.

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32

Penen, F., M. P. Isaure, D. Dobritzsch, et al. "Pools of cadmium in Chlamydomonas reinhardtii revealed by chemical imaging and XAS spectroscopy." Metallomics 9, no. 7 (2017): 910–23. http://dx.doi.org/10.1039/c7mt00029d.

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33

Hu, Shengxi, Ken W. K. Lau, and Madeline Wu. "Cadmium sequestration in Chlamydomonas reinhardtii." Plant Science 161, no. 5 (2001): 987–96. http://dx.doi.org/10.1016/s0168-9452(01)00501-5.

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34

Gfeller, Rene P., and Martin Gibbs. "Fermentative Metabolism of Chlamydomonas reinhardtii." Plant Physiology 77, no. 2 (1985): 509–11. http://dx.doi.org/10.1104/pp.77.2.509.

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35

Maul, Jude E., Jason W. Lilly, Liying Cui, et al. "The Chlamydomonas reinhardtii Plastid Chromosome." Plant Cell 14, no. 11 (2002): 2659–79. http://dx.doi.org/10.1105/tpc.006155.

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36

Beck, Christoph F., and Axel Acker. "Gametic Differentiation of Chlamydomonas reinhardtii." Plant Physiology 98, no. 3 (1992): 822–26. http://dx.doi.org/10.1104/pp.98.3.822.

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37

SILFLOW, CAROLYN D., and JAMES YOUNGBLOM. "Chlamydomonas reinhardtii Tubulin Gene Structure." Annals of the New York Academy of Sciences 466, no. 1 Dynamic Aspec (1986): 18–30. http://dx.doi.org/10.1111/j.1749-6632.1986.tb38381.x.

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38

Zhu, Chi, Chuanhong Chen, Liangyuan Zhao, et al. "Bioflocculant produced by Chlamydomonas reinhardtii." Journal of Applied Phycology 24, no. 5 (2011): 1245–51. http://dx.doi.org/10.1007/s10811-011-9769-x.

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39

Holmes, J. A., and S. K. Dutcher. "Cellular asymmetry in Chlamydomonas reinhardtii." Journal of Cell Science 94, no. 2 (1989): 273–85. http://dx.doi.org/10.1242/jcs.94.2.273.

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Although largely bilaterally symmetric, the two sides of the unicellular alga Chlamydomonas reinhardtii can be distinguished by the location of the single eyespot. When viewed from the anterior end, the eyespot is always closer to one flagellum than the other, and located at an angle of approximately 45 degrees clockwise of the flagellar plane. This location correlates with the position of one of four acetylated microtubule bundles connected to the flagellar apparatus. Each basal body is attached to two of these microtubule rootlets. The rootlet that positions the eyespot is always attached to

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40

Rupaedah, Bedah, and Yuichiro Takahashi. "EFFECT OF NITROGEN SUPPLY IN CULTURE MEDIA AND LIGHT INTENSITY ON PHOTOSYNTHESIS OF Chlamydomonas reinhardtii." Jurnal Bioteknologi & Biosains Indonesia (JBBI) 4, no. 2 (2017): 11. http://dx.doi.org/10.29122/jbbi.v4i2.15.

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Pengaruh Suplai Nitrogen pada Media Kultur dan Intensitas Cahaya Terhadap Proses Fotosintesis Chlamydomonas reinhardtiiOrganisms use nitrogen to produce, among others, amino acids, proteins, and nucleic acids. In this study, the effects of various concentrations of ammonium in culture media on the photosynthetic performance of Chlamydomonas reinhardtii were done under two light conditions: low and high intensity. The microbes were grown at low (75% NH4Cl dosage), normal (100% NH4Cl dosage, which was 2 M NH4Cl), and high (125% NH4Cl dosage) nitrogen content. Cells density and chlorophyll conten

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Yu, Zhen, Huiling Wei, Rui Hao, Huashuo Chu, and Yi Zhu. "Physiological changes in Chlamydomonas reinhardtii after 1000 generations of selection of cadmium exposure at environmentally relevant concentrations." Environmental Science: Processes & Impacts 20, no. 6 (2018): 923–33. http://dx.doi.org/10.1039/c8em00106e.

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Shitanda, Isao, Koji Tanaka, Yoshinao Hoshi, and Masayuki Itagaki. "Electrochemical monitoring systems of demembranated flagellate algal motility for ATP sensing." Analyst 139, no. 4 (2014): 721–23. http://dx.doi.org/10.1039/c3an01678a.

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Remacle, C., F. Duby, P. Cardol, and R. F. Matagne. "Mutations inactivating mitochondrial genes in Chlamydomonas reinhardtii." Biochemical Society Transactions 29, no. 4 (2001): 442–46. http://dx.doi.org/10.1042/bst0290442.

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Chlamydomonas reinhardtii is now becoming a useful model for the study of mitochondrial genetics in a photosynthetic organism. The small (15.8 kb) mitochondrial genome C. reinhardtii has been sequenced completely and all the genes have been identified. Several mutants inactivated in mitochondrial genes encoding components of the respiratory complexes I, III and IV have been characterized at the molecular level. Assembly of complex I in several mutant strains and mapping of mitochondrial mutations by recombinational analysis are also described.

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GOODENOUGH, URSULA W., and JOHN E. HEUSER. "Molecular organization of cell-wall crystals from Chlamydomonas reinhardtii and Volvox carteri." Journal of Cell Science 90, no. 4 (1988): 717–34. http://dx.doi.org/10.1242/jcs.90.4.717.

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The extracellular matrices of Chlamydomonas reinhardtii and Volvox carteri contain homologous salt-extractable crystalline layers that will self-assemble in vitro. The organization of these crystals is examined using the quick-freeze deepetch technique. In C. reinhardtii, the outer layer of the crystal is an open polygonal weave (W6B); this is shown to be constructed from regular overlapping associations between the fibrous hydroxyproline-rich glycoprotein GP1. The inner layer of the crystal (W6A) is shown to be a copolymer of GP2 and GP3. The bulky globular domains of these glycoproteins form

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Tainio, Oskar, Fereshteh Sohrabi, Nikodem Janarek, et al. "Correction: Chlamydomonas reinhardtii swimming in the Plateau borders of 2D foams." Soft Matter 17, no. 27 (2021): 6675. http://dx.doi.org/10.1039/d1sm90118d.

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46

Cui, Mingyang, Minji Kim, Patricia B. Weisensee, and J. Mark Meacham. "Thermal considerations for microswimmer trap-and-release using standing surface acoustic waves." Lab on a Chip 21, no. 13 (2021): 2534–43. http://dx.doi.org/10.1039/d1lc00257k.

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47

Posewitz, M. C., P. W. King, S. L. Smolinski, et al. "Identification of genes required for hydrogenase activity in Chlamydomonas reinhardtii." Biochemical Society Transactions 33, no. 1 (2005): 102–4. http://dx.doi.org/10.1042/bst0330102.

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The eukaryotic green alga, Chlamydomonas reinhardtii, produces H2 under anaerobic conditions, in a reaction catalysed by an [FeFe]-hydrogenase. To identify genes that influence H2 production in C. reinhardtii, a library of 6000 colonies on agar plates was screened with sensitive chemochromic H2-sensor films for clones defective in H2 production. Two mutants of particular interest were fully characterized. One mutant, hydEF-1, is unable to assemble an active [FeFe]-hydrogenase. This is the first reported C. reinhardtii mutant that is not capable of producing any H2. The second mutant, sta7-10,

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48

PRÖSCHOLD, THOMAS, TATYANA DARIENKO, LOTHAR KRIENITZ, and ANNETTE W. COLEMAN. "Chlamydomonas schloesseri sp. nov. (Chlamydophyceae, Chlorophyta) revealed by morphology, autolysin cross experiments, and multiple gene analyses." Phytotaxa 362, no. 1 (2018): 21. http://dx.doi.org/10.11646/phytotaxa.362.1.2.

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Chlamydomonas in the traditional sense is one of the largest green algal genera, comprising more than 500 described species. However, since the designation of the model organism C. reinhardtii as conserved type of this genus in 2007, only two species remained in Chlamydomonas. Investigations of three new strains isolated from soil samples, which were collected near Lake Nakuru (Kenya), demonstrated that the isolates represent a new species of Chlamydomonas. Phylogenetic analyses of nuclear SSU and ITS rDNA and plastid-coding rbcL sequences have clearly revealed that this species is closely rel

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Ibuot, Aniefon, Andrew P. Dean, and Jon K. Pittman. "Multi-genomic analysis of the cation diffusion facilitator transporters from algae." Metallomics 12, no. 4 (2020): 617–30. http://dx.doi.org/10.1039/d0mt00009d.

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Abstract:

Cation diffusion facilitator metal transporters are widespread throughout algae and include a novel algal-specific clade. Functional analysis of Chlamydomonas reinhardtii isoforms partly validated phylogenetic prediction of substrate specificity.

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Kim, Minji, Philip V. Bayly, and J. Mark Meacham. "Motile cells as probes for characterizing acoustofluidic devices." Lab on a Chip 21, no. 3 (2021): 521–33. http://dx.doi.org/10.1039/d0lc01025a.

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Dynamically responsive Chlamydomonas reinhardtii algae cells enable real-time assessment of acoustofluidic device performance. The steady-state distribution of these motile cells reflects both the field shape and strength.

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