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Journal articles on the topic 'Green Alga Bottryococcus braunii'

Author: Grafiati

Published: 6 September 2023

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1

YAMAGUCHI, Katsumi, Hiroshi NAKANO, Masahiro MURAKAMI, Shoji KONOSU, Osamu NAKAYAMA, Midori KANDA, Akihiro NAKAMURA, and Hiroaki IWAMOTO. "Lipid composition of a green alga, Botryococcus braunii." Agricultural and Biological Chemistry 51, no. 2 (1987): 493–98. http://dx.doi.org/10.1271/bbb1961.51.493.

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2

Yamaguchi, Katsumi, Hiroshi Nakano, Masahiro Murakami, Shoji Konosu, Osamu Nakayama, Midori Kanda, Akihiro Nakamura, and Hiroaki Iwamoto. "Lipid Composition of a Green Alga,Botryococcus braunii." Agricultural and Biological Chemistry 51, no. 2 (February 1987): 493–98. http://dx.doi.org/10.1080/00021369.1987.10868040.

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3

Bollman, R. C., and G. G. C. Robinson. "Heterotrophic potential of the green alga, Ankistrodesmus braunii (Naeg.)." Canadian Journal of Microbiology 31, no. 6 (June 1, 1985): 549–54. http://dx.doi.org/10.1139/m85-102.

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The green alga, Ankistrodesmus braunii (Naeg.), was found to possess a biphasic transport system for D-glucose. The high affinity component of the system had a Vmax of 1.2 × 10−7 pmol∙cell−1∙min−1 and a specific transport constant (Kt) of 7.7 nM glucose. The low-affinity component had a Vmax of 10.8 × 10−4 pmol∙cell−1∙min−1 at a Kt of 16.2 μM glucose. These kinetic values indicate that the alga could compete successfully with bacteria for glucose in natural waters. Ankistrodesmus braunii also grew heterotrophically on 0.1 mM glucose with a doubling time of 31.4 h. The growth rate was shown to correspond with the transport rate when an excretion rate of 3.5% and a respiration rate of 48% of the transported glucose were considered.

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4

Vazquez-Duhalt, Rafael, and Bertha O. Arredondo-Vega. "Haloadaptation of the green alga Botryococcus braunii (race a)." Phytochemistry 30, no. 9 (January 1991): 2919–25. http://dx.doi.org/10.1016/s0031-9422(00)98225-6.

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5

Metzger, P., E. Casadevall, and A. Coute. "Botryococcene distribution in strains of the green alga Botryococcus braunii." Phytochemistry 27, no. 5 (January 1988): 1383–88. http://dx.doi.org/10.1016/0031-9422(88)80199-7.

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6

Summons, RE, and RJ Capon. "Botryococcenone, an Oxygenated Botryococcene From Botryococcus braunii." Australian Journal of Chemistry 44, no. 2 (1991): 313. http://dx.doi.org/10.1071/ch9910313.

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A new botryococcene (5) incorporating an unprecedented ketone functionality has been identified in the lipid extract of an Australian collection of the green alga Botryococcus braunii Kutzing . The structure was established by detailed n.m.r. and mass spectroscopic analysis. A saturated hydrocarbon (8) prepared from this ketone by catalytic hydrogenation and Wolff-Kishner reduction has a different carbon skeleton to that of (9) prepared by hydrogenation of the co-occurring C33 botryococcene.

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7

van den Berg, Tomas E., Volha U. Chukhutsina, Herbert van Amerongen, Roberta Croce, and Bart van Oort. "Light Acclimation of the Colonial Green Alga Botryococcus braunii Strain Showa." Plant Physiology 179, no. 3 (January 16, 2019): 1132–43. http://dx.doi.org/10.1104/pp.18.01499.

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8

García-Fernández, J. M., A. López-Ruiz, J. Alhama, and J. Diez. "Light regulation of glutamine synthetase in the green alga Monoraphidium braunii." Journal of Plant Physiology 146, no. 5-6 (September 1995): 577–83. http://dx.doi.org/10.1016/s0176-1617(11)81917-6.

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9

Hirose, Mana, Fukiko Mukaida, Sigeru Okada, and Tetsuko Noguchi. "Active Hydrocarbon Biosynthesis and Accumulation in a Green Alga, Botryococcus braunii (Race A)." Eukaryotic Cell 12, no. 8 (June 21, 2013): 1132–41. http://dx.doi.org/10.1128/ec.00088-13.

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ABSTRACT Among oleaginous microalgae, the colonial green alga Botryococcus braunii accumulates especially large quantities of hydrocarbons. This accumulation may be achieved more by storage of lipids in the extracellular space rather than in the cytoplasm, as is the case for all other examined oleaginous microalgae. The stage of hydrocarbon synthesis during the cell cycle was determined by autoradiography. The cell cycle of B. braunii race A was synchronized by aminouracil treatment, and cells were taken at various stages in the cell cycle and cultured in a medium containing [ 14 C]acetate. Incorporation of 14 C into hydrocarbons was detected. The highest labeling occurred just after septum formation, when it was about 2.6 times the rate during interphase. Fluorescent and electron microscopy revealed that new lipid accumulation on the cell surface occurred during at least two different growth stages and sites of cells. Lipid bodies in the cytoplasm were not prominent in interphase cells. These lipid bodies then increased in number, size, and inclusions, reaching maximum values just before the first lipid accumulation on the cell surface at the cell apex. Most of them disappeared from the cytoplasm concomitant with the second new accumulation at the basolateral region, where extracellular lipids continuously accumulated. The rough endoplasmic reticulum near the plasma membrane is prominent in B. braunii , and the endoplasmic reticulum was often in contact with both a chloroplast and lipid bodies in cells with increasing numbers of lipid bodies. We discuss the transport pathway of precursors of extracellular hydrocarbons in race A.

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10

Wünschiers, Röbbe, Thomas Zinn, Dietmar Linder, and Rüdiger Schulz. "Purification and Characterization of Cytochrome c6 from the Unicellular Green Alga Scenedesmus obliquus." Zeitschrift für Naturforschung C 52, no. 11-12 (December 1, 1997): 740–46. http://dx.doi.org/10.1515/znc-1997-11-1204.

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Abstract Purification of a soluble cytochrome c6 from the unicellular green alga Scenedesmus obliquus by a simple and rapid method is described. The purification procedure includes ammonium sulfate precipitation and non-denaturating PAGE. The N-terminal sequence of the first 20 amino acids was determined and shows 85% similarity and 75% identity to the sequence of cytochrome c6 from the green alga Monoraphidium braunii. The ferrocyto-chrome shows typical UV/VIS absorption peaks at 552.9, 521.9 and 415.7 nm. The apparent molecular mass was estimated to be 12 kD a by SDS-PAGE. EPR-spectroscopy at 20K shows resonances indicative for two distinct low-spin heme forms.

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11

García-Fernández, JoséManuel, Antonio López-Ruiz, Lourdes Humanes, and Jesús Diez Dapena. "Purification and characterization of glutamine synthetase from the green alga Monoraphidium braunii." Plant Science 123, no. 1-2 (March 1997): 77–84. http://dx.doi.org/10.1016/s0168-9452(96)04580-3.

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12

David, M., P. Metzger, and E. Casadevall. "Two cyclobotryococcenes from the B race of the green alga Botryococcus braunii." Phytochemistry 27, no. 9 (January 1988): 2863–67. http://dx.doi.org/10.1016/0031-9422(88)80677-0.

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13

Zou, Jiajun, and Guiqi Bi. "Complete mitochondrial genome of a hydrocarbon-producing green alga Botryococcus braunii strain Showa." Mitochondrial DNA Part A 27, no. 4 (June 29, 2015): 2619–20. http://dx.doi.org/10.3109/19401736.2015.1041122.

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14

An, Jin-Young, Sang-Jun Sim, Jin Suk Lee, and Byung Woo Kim. "Hydrocarbon production from secondarily treated piggery wastewater by the green alga Botryococcus braunii." Journal of Applied Phycology 15, no. 2/3 (March 2003): 185–91. http://dx.doi.org/10.1023/a:1023855710410.

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15

Metzger, P., and E. Casadevall. "Lycopadiene, a tetraterpenoid hydrocarbon from new strains of the green alga Botryococcus braunii." Tetrahedron Letters 28, no. 34 (January 1987): 3931–34. http://dx.doi.org/10.1016/s0040-4039(00)96423-2.

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16

Corzo, Alfonso, Reiner Plasa, and Wolfram R. Ullrich. "Extracellular ferricyanide reduction and nitrate reductase activity in the green alga Monoraphidium braunii." Plant Science 75, no. 2 (January 1991): 221–28. http://dx.doi.org/10.1016/0168-9452(91)90237-3.

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17

Humanes, Lourdes, JoséManuel García-Fernández, Antonio López-Ruiz, and Jesús Diez. "Glutamine synthetase from the green alga Monoraphidium braunii is regulated by oxidative modification." Plant Science 110, no. 2 (September 1995): 269–77. http://dx.doi.org/10.1016/0168-9452(95)04197-3.

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18

Banci, Lucia, I. Bertini, G. Quacquarini, Olaf Walter, Antonio Díaz, Manuel Hervás, and Miguel A. de la Rosa. "The solution structure of cytochrome c 6 from the green alga Monoraphidium braunii." JBIC Journal of Biological Inorganic Chemistry 1, no. 4 (August 1996): 330–40. http://dx.doi.org/10.1007/s007750050061.

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19

Li, Y., R. B. Moore, J. G. Qin, A. Scott, and A. S. Ball. "Extractable liquid, its energy and hydrocarbon content in the green alga Botryococcus braunii." Biomass and Bioenergy 52 (May 2013): 103–12. http://dx.doi.org/10.1016/j.biombioe.2013.03.002.

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20

Rao, A. Ranga, C. Dayananda, R. Sarada, T. R. Shamala, and G. A. Ravishankar. "Effect of salinity on growth of green alga Botryococcus braunii and its constituents." Bioresource Technology 98, no. 3 (February 2007): 560–64. http://dx.doi.org/10.1016/j.biortech.2006.02.007.

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21

Grung, Merete, Pierre Metzger, and Synnove Liaaen-jensen. "Primary and secondary carotenoids in two races of the green alga Botryococcus braunii." Biochemical Systematics and Ecology 17, no. 4 (July 1989): 263–69. http://dx.doi.org/10.1016/0305-1978(89)90001-x.

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22

Dayananda, Chandrappa, Ravi Sarada, Vinod Kumar, and Gokare Aswathanarayana Ravishankar. "Isolation and characterization of hydrocarbon producing green alga Botryococcus braunii from Indian freshwater bodies." Electronic Journal of Biotechnology 10, no. 1 (January 15, 2007): 0. http://dx.doi.org/10.2225/vol10-issue1-fulltext-11.

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23

Garcia-Fernandez, J. M., A. Lopez-Ruiz, F. Toribio, J. M. Roldan, and J. Diez. "Occurrence of Only One Form of Glutamine Synthetase in the Green Alga Monoraphidium braunii." Plant Physiology 104, no. 2 (February 1, 1994): 425–30. http://dx.doi.org/10.1104/pp.104.2.425.

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24

Lin, Rui, and G. Patrick Ritz. "Reflectance FT-IR Microspectroscopy of Fossil Algae Contained in Organic-Rich Shales." Applied Spectroscopy 47, no. 3 (March 1993): 265–71. http://dx.doi.org/10.1366/0003702934066794.

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A microscope sampling accessory interfaced to a Fourier transform infrared (FT-IR) spectrometer has been employed to characterize the remains of individual microscopic fossil algae and algal colonies contained in organic-rich shales. The microspectrometer is able to measure reflectance IR spectra of samples with cross-sectional areas as small as 20 × 20 microns. The fossil algae studied include the colonial green alga Botryococcus braunii, the unicellular green alga Tasmanites, and an unidentified filamentous alga. It was found that IR spectra of the fossil algae, in common, contain intense aliphatic C-H stretching bands in the 2900-cm−1 region relative to the C=C stretching band at 1600 cm−1. The carboxylic acid C=O stretching band at 1710 cm−1 is moderately intense. The relative intensities of these bands vary among the three different fossil algae. Maximum-likelihood spectral restoration and subsequent curve fitting of the stretching vibrations of the aliphatic C-H bands provide greater insight into the aliphatic structures of fossil algae. The CH2/CH3 intensity ratio can be calculated and used to assess the relative average aliphatic chain length and the degree of branching.

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25

Noguchi, Tetsuko, and Fukiko Kakami. "Transformation of trans-Golgi Network During the Cell Cycle in a Green Alga, Botryococcus braunii." Journal of Plant Research 112, no. 2 (June 1999): 175–86. http://dx.doi.org/10.1007/pl00013871.

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26

Xu, Zhenyu, Jing He, Shuyuan Qi, and Jianhua Liu. "Nitrogen deprivation-induced de novo transcriptomic profiling of the oleaginous green alga Botryococcus braunii 779." Genomics Data 6 (December 2015): 231–33. http://dx.doi.org/10.1016/j.gdata.2015.09.019.

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27

Suzuki, Reiko, Ichiro Nishii, Shigeru Okada, and Tetsuko Noguchi. "3D reconstruction of endoplasmic reticulum in a hydrocarbon-secreting green alga, Botryococcus braunii (Race B)." Planta 247, no. 3 (November 22, 2017): 663–77. http://dx.doi.org/10.1007/s00425-017-2811-8.

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28

Wang, Xing, and Pappachan E. Kolattukudy. "Solubilization and purification of aldehyde-generating fatty acyl-CoA reductase from green alga Botryococcus braunii." FEBS Letters 370, no. 1-2 (August 14, 1995): 15–18. http://dx.doi.org/10.1016/0014-5793(95)00781-4.

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29

Arya, Anju, Khushbu Gupta, Tejpal Singh Chundawat, and Dipti Vaya. "Biogenic Synthesis of Copper and Silver Nanoparticles Using Green Alga Botryococcus braunii and Its Antimicrobial Activity." Bioinorganic Chemistry and Applications 2018 (October 21, 2018): 1–9. http://dx.doi.org/10.1155/2018/7879403.

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The spread of infectious diseases and the increase in the drug resistance among microbes has forced the researchers to synthesize biologically active nanoparticles. Improvement of the ecofriendly procedure for the synthesis of nanoparticles is growing day-by-day in the field of nanobiotechnology. In the present study, we use the extract of green alga Botryococcus braunii for the synthesis of copper and silver nanoparticles. The characterization of copper and silver nanoparticles was carried out by using UV-Vis spectroscopy, Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and scanning electron spectroscopy (SEM). FTIR measurements showed all functional groups having control over reduction and stabilization of the nanoparticles. The X-ray diffraction pattern revealed that the particles were crystalline in nature with a face-centred cubic (FCC) geometry. SEM micrographs have shown the morphology of biogenically synthesized metal nanoparticles. Furthermore, these biosynthesized nanoparticles were found to be highly toxic against two Gram-negative bacterial strains Pseudomonas aeruginosa (MTCC 441) and Escherichia coli (MTCC 442), two Gram-positive bacterial strains Klebsiella pneumoniae (MTCC 109) and Staphylococcus aureus (MTCC 96), and a fungal strain Fusarium oxysporum (MTCC 2087). The zone of inhibition was measured by the agar well plate method, and furthermore, minimum inhibitory concentration was determined by the broth dilution assay.

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30

Lee, Kim, Kim, Kwon, Yoon, and Oh. "Effects of harvesting method and growth stage on the flocculation of the green alga Botryococcus braunii." Letters in Applied Microbiology 27, no. 1 (July 1998): 14–18. http://dx.doi.org/10.1046/j.1472-765x.1998.00375.x.

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31

Metzger, P. "Structures of some botryococcenes: branched hydrocarbons from the b-race of the green alga Botryococcus braunii." Phytochemistry 23, no. 12 (November 26, 1985): 2995–3002. http://dx.doi.org/10.1016/s0031-9422(00)80621-4.

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32

Metzger, P., E. Villarreal-Rosales, E. Casadevall, and A. Coute. "Hydrocarbons, aldehydes and triacylglycerols in some strains of the arace of the green alga Botryococcus braunii." Phytochemistry 28, no. 9 (January 1989): 2349–53. http://dx.doi.org/10.1016/s0031-9422(00)97982-2.

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33

Suzuki, Reiko, Naoko Ito, Yuki Uno, Ichiro Nishii, Satoshi Kagiwada, Sigeru Okada, and Tetsuko Noguchi. "Transformation of Lipid Bodies Related to Hydrocarbon Accumulation in a Green Alga, Botryococcus braunii (Race B)." PLoS ONE 8, no. 12 (December 5, 2013): e81626. http://dx.doi.org/10.1371/journal.pone.0081626.

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34

Song, Liang, Jian G. Qin, Shengqi Su, Jianhe Xu, Stephen Clarke, and Yichu Shan. "Micronutrient Requirements for Growth and Hydrocarbon Production in the Oil Producing Green Alga Botryococcus braunii (Chlorophyta)." PLoS ONE 7, no. 7 (July 25, 2012): e41459. http://dx.doi.org/10.1371/journal.pone.0041459.

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35

Baba, Masato, Fumie Kikuta, Iwane Suzuki, Makoto M. Watanabe, and Yoshihiro Shiraiwa. "Wavelength specificity of growth, photosynthesis, and hydrocarbon production in the oil-producing green alga Botryococcus braunii." Bioresource Technology 109 (April 2012): 266–70. http://dx.doi.org/10.1016/j.biortech.2011.05.059.

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36

Metzger, P., E. Casadevall, M. J. Pouet, and Y. Pouet. "Structures of some botryococcenes: branched hydrocarbons from the b-race of the green alga Botryococcus braunii." Phytochemistry 24, no. 12 (November 1985): 2995–3002. http://dx.doi.org/10.1016/0031-9422(85)80043-1.

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37

Natalia O., Zhila, Kalachova Galina S., and Volova Tatiana G. "Influence of Salinity on Growth and Biochemical Composition of Green Alga Botryococcus braunii Kütz IPPAS H-252." Journal of Siberian Federal University. Biology 4, no. 3 (September 2011): 229–42. http://dx.doi.org/10.17516/1997-1389-0167.

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38

Aparicio, Pedro J., and Miguel A. Quiñones. "Blue Light, a Positive Switch Signal for Nitrate and Nitrite Uptake by the Green Alga Monoraphidium braunii." Plant Physiology 95, no. 2 (February 1, 1991): 374–78. http://dx.doi.org/10.1104/pp.95.2.374.

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39

Weiss, Taylor L., Robyn Roth, Carrie Goodson, Stanislav Vitha, Ian Black, Parastoo Azadi, Jannette Rusch, Andreas Holzenburg, Timothy P. Devarenne, and Ursula Goodenough. "Colony Organization in the Green Alga Botryococcus braunii (Race B) Is Specified by a Complex Extracellular Matrix." Eukaryotic Cell 11, no. 12 (August 31, 2012): 1424–40. http://dx.doi.org/10.1128/ec.00184-12.

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ABSTRACTBotryococcus brauniiis a colonial green alga whose cells associate via a complex extracellular matrix (ECM) and produce prodigious amounts of liquid hydrocarbons that can be readily converted into conventional combustion engine fuels. We used quick-freeze deep-etch electron microscopy and biochemical/histochemical analysis to elucidate many new features ofB. brauniicell/colony organization and composition. Intracellular lipid bodies associate with the chloroplast and endoplasmic reticulum (ER) but show no evidence of being secreted. The ER displays striking fenestrations and forms a continuous subcortical system in direct contact with the cell membrane. The ECM has three distinct components. (i) Each cell is surrounded by a fibrous β-1, 4- and/or β-1, 3-glucan-containing cell wall. (ii) The intracolonial ECM space is filled with a cross-linked hydrocarbon network permeated with liquid hydrocarbons. (iii) Colonies are enclosed in a retaining wall festooned with a fibrillar sheath dominated by arabinose-galactose polysaccharides, which sequesters ECM liquid hydrocarbons. Each cell apex associates with the retaining wall and contributes to its synthesis. Retaining-wall domains also form “drapes” between cells, with some folding in on themselves and penetrating the hydrocarbon interior of a mother colony, partitioning it into daughter colonies. We propose that retaining-wall components are synthesized in the apical Golgi apparatus, delivered to apical ER fenestrations, and assembled on the surfaces of apical cell walls, where a proteinaceous granular layer apparently participates in fibril morphogenesis. We further propose that hydrocarbons are produced by the nonapical ER, directly delivered to the contiguous cell membrane, and pass across the nonapical cell wall into the hydrocarbon-based ECM.

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40

Metzger, P., J. Templier, C. Largeau, and E. Casadevall. "An n-alkatriene and some n-alkadienes from the A race of the green alga Botryococcus braunii." Phytochemistry 25, no. 8 (July 1986): 1869–72. http://dx.doi.org/10.1016/s0031-9422(00)81165-6.

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41

Kagiwada, Satoshi, Sayuri Sugita, Yuka Masaike, Sakiko Kato, and Tetsuko Noguchi. "Characterization of coat proteins of COPI- and clathrin-coated vesicles in the unicellular green alga Botryococcus braunii." Plant Science 169, no. 4 (October 2005): 668–79. http://dx.doi.org/10.1016/j.plantsci.2005.05.027.

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42

KAWAHARA, Kengo, Masaki SAGEHASHI, Takao FUJII, Hirotaka FUJITA, Hong-Ying HU, and Akiyoshi SAKODA. "Potential of a Green Alga Botryococcus braunii for Simultaneous Water Purification and Biofuel Production under Open-Air Condition." Journal of Water and Environment Technology 9, no. 1 (2011): 29–37. http://dx.doi.org/10.2965/jwet.2011.29.

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43

APARICIO, P. J., F. G. WITT, J. M. RAMIREZ, M. A. QUINONES, and T. BALANDIN. "Blue-light-induced pH changes associated with NO3-, NO2- and Cl- uptake by the green alga Monoraphidium braunii." Plant, Cell and Environment 17, no. 12 (December 1994): 1323–30. http://dx.doi.org/10.1111/j.1365-3040.1994.tb00534.x.

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44

Gattullo, C. Eliana, Hanno Bährs, Christian E. W. Steinberg, and Elisabetta Loffredo. "Removal of bisphenol A by the freshwater green alga Monoraphidium braunii and the role of natural organic matter." Science of The Total Environment 416 (February 2012): 501–6. http://dx.doi.org/10.1016/j.scitotenv.2011.11.033.

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45

Metzger, Pierre, and Eliette Casadevall. "Botryals, even C52-C64 aldehydes from aldol condensation, in the a race of the green alga botryococcus Braunii." Tetrahedron Letters 29, no. 23 (January 1988): 2831–34. http://dx.doi.org/10.1016/0040-4039(88)85223-7.

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46

Song, Liang, Jian G. Qin, Stephen Clarke, and Yan Li. "Competition and succession between the oily alga Botryococcus braunii and two green algae Chlorella vulgaris and Chlamydomonas reinhardtii." Journal of Applied Phycology 25, no. 3 (November 11, 2012): 847–53. http://dx.doi.org/10.1007/s10811-012-9940-z.

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47

Tanabe, Yuuhiko, Motohide Ioki, and Makoto M. Watanabe. "The fast-growing strain of hydrocarbon-rich green alga Botryococcus braunii, BOT-22, is a vitamin B12 autotroph." Journal of Applied Phycology 26, no. 1 (May 12, 2013): 9–13. http://dx.doi.org/10.1007/s10811-013-0045-0.

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48

Uno, Yuki, Ichiro Nishii, Satoshi Kagiwada, and Tetsuko Noguchi. "Colony sheath formation is accompanied by shell formation and release in the green alga Botryococcus braunii (race B)." Algal Research 8 (March 2015): 214–23. http://dx.doi.org/10.1016/j.algal.2015.02.015.

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49

Ranga Rao, A., G. A. Ravishankar, and R. Sarada. "Cultivation of green alga Botryococcus braunii in raceway, circular ponds under outdoor conditions and its growth, hydrocarbon production." Bioresource Technology 123 (November 2012): 528–33. http://dx.doi.org/10.1016/j.biortech.2012.07.009.

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50

Alhama, José, Antonio López-Ruiz, Jesús Diez, and José Manuel García-Fernández. "Effect of carbon and nitrogen availability on intracellular amino acids and ammonium pools in the green alga Monoraphidium braunii." Journal of Plant Physiology 153, no. 5-6 (January 1998): 529–33. http://dx.doi.org/10.1016/s0176-1617(98)80199-5.

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