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Journal articles on the topic 'Bienertia sinuspersici'

Author: Grafiati

Published: 4 June 2021

Last updated: 9 February 2022

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1

Kim, Beomsoo, Jingyu Kim, Hyun Park, and Joonho Park. "The complete chloroplast genome sequence of Bienertia sinuspersici." Mitochondrial DNA Part B 1, no. 1 (January 1, 2016): 388–89. http://dx.doi.org/10.1080/23802359.2016.1174083.

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2

Soundararajan, Prabhakaran, So Youn Won, Dong Suk Park, Yeon-Hee Lee, and Jung Sun Kim. "Comparative Analysis of the YABBY Gene Family of Bienertia sinuspersici, a Single-Cell C4 Plant." Plants 8, no. 12 (November 22, 2019): 536. http://dx.doi.org/10.3390/plants8120536.

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The emergence and expression of the YABBY gene family (YGF) coincided with the evolution of leaves in seed plants, and was integral to the early evidence of lamina followed by reproductive development. YGF contains six subclasses, i.e., CRC, INO, FIL, YAB2, YAB3, and YAB5. This study aims to extract the genome sequences of the YGF in Bienertia sinuspersici, an important model plant for single-cell C4 (SCC4), non-Kranz photosynthesis. A comparative genomic analysis was undertaken with Vitis vinefera, Arabidopsis thaliana, Brassica rapa, and Chenopodium quinoa. Six copies of YGF were present in B. sinuspersici and A. thaliana with a single copy of each YGF subgroup. V. vinefera possessed seven copies of YGF with duplicates in FIL and YAB2 subgroups, but no YAB3. B. rapa and C. quinoa after whole genome duplication contained additional copies of YGF. The gene structure and conserved motifs were analyzed among the YGF. In addition, the relative quantification of YGF was analyzed in the leaves, reproductive developmental stages such as the bud, and the pre-anthesis and anthesis stages in B. sinuspersici, A. thaliana, and B. rapa. CRC and INO possessed conserved floral-specific expression. Temporal and perpetual changes in the expression of YGF orthologs were observed in the leaves and reproductive developmental stages. The results of this study provide an overview of YGF evolution, copy number, and its differential expression in B. sinuspersici. Further studies are required to shed light on the roles of YABBY genes in the evolution of SCC4 plants and their distinct physiologies.

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3

Lung, Shiu-Cheung, Makoto Yanagisawa, and Simon DX Chuong. "Isolation of dimorphic chloroplasts from the single-cell C4 species Bienertia sinuspersici." Plant Methods 8, no. 1 (2012): 8. http://dx.doi.org/10.1186/1746-4811-8-8.

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4

Park, Joonho, Thomas W. Okita, and Gerald E. Edwards. "Expression profiling and proteomic analysis of isolated photosynthetic cells of the non-Kranz C4 species Bienertia sinuspersici." Functional Plant Biology 37, no. 1 (2010): 1. http://dx.doi.org/10.1071/fp09074.

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Bienertia sinuspersici Akhani represents one form of C4 photosynthesis that occurs without Kranz anatomy in family Chenopodiaceae. Analysis of transcript profiles and proteomics were made to gain information on this single-cell C4 photosynthetic mechanism. Chlorenchyma cells were isolated and purified from mature leaves. From these cells, a cDNA library was made from which sequences were obtained on 2385 clones using conventional methods. To obtain a protein profile, the multi dimensional protein identification technique was used, resulting in identification of 322 unique proteins in chlorenchyma cells. After analysing datasets from the EST library and proteomics, genes and proteins were classified into 23 and 17 categories according to types of biological processes, respectively. These include photosynthesis and photorespiration, other biosynthetic and metabolic processes, cell wall modification, defence response, DNA repair, electron transport, other cellular and developmental processes, protein folding, protein targeting, protein modification, proteolysis, redox and ion homeostasis, response to biotic and abiotic stresses, RNA modification, transcription, translation, transport and unknowns. Sequence and phylogenetic analyses were made of C4 cycle enzymes to characterise the relationship between homologues found in Bienertia with public gene sequences from other chenopods and representative C3 and C4 species from other families. Identified photosynthetic genes and proteins are discussed with respect to the proposed function of an NAD-ME type C4 cycle in this single-cell C4 system.

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5

Northmore, Jennifer Anne, Marie Leung, and Simon Dich Xung Chuong. "Effects of Media Composition and Auxins on Adventitious Rooting of Bienertia sinuspersici Cuttings." Advances in Bioscience and Biotechnology 06, no. 10 (2015): 629–36. http://dx.doi.org/10.4236/abb.2015.610066.

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6

Sevilleno, Samantha Serafin, Yoon Ha Ju, Jung Sun Kim, Franklin Hinosa Mancia, Eun Ju Byeon, Raisa Aone Cabahug, and Yoon-Jung Hwang. "Cytogenetic analysis of Bienertia sinuspersici Akhani as the first step in genome sequencing." Genes & Genomics 42, no. 3 (January 4, 2020): 337–45. http://dx.doi.org/10.1007/s13258-019-00908-5.

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7

Shwaish, Tarik, Faris JM Al-Imarah, and Fatimah A. Jasim. "Wound Healing Capacity, Antibacterial Activity, and GC-MS Analysis of Bienertia sinuspersici Leaves Extract." Journal of Physics: Conference Series 1294 (September 2019): 062056. http://dx.doi.org/10.1088/1742-6596/1294/6/062056.

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8

Northmore, Jennifer Anne, Victoria Zhou, and Simon D. X. Chuong. "Multiple shoot induction and plant regeneration of the single-cell C4 species Bienertia sinuspersici." Plant Cell, Tissue and Organ Culture (PCTOC) 108, no. 1 (August 21, 2011): 101–9. http://dx.doi.org/10.1007/s11240-011-0018-4.

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9

Park, Joonho, Thomas W. Okita, and Gerald E. Edwards. "Salt tolerant mechanisms in single-cell C4 species Bienertia sinuspersici and Suaeda aralocaspica (Chenopodiaceae)." Plant Science 176, no. 5 (May 2009): 616–26. http://dx.doi.org/10.1016/j.plantsci.2009.01.014.

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10

Lung, Shiu-Cheung, Makoto Yanagisawa, and Simon D. X. Chuong. "Protoplast isolation and transient gene expression in the single-cell C4 species, Bienertia sinuspersici." Plant Cell Reports 30, no. 4 (November 20, 2010): 473–84. http://dx.doi.org/10.1007/s00299-010-0953-2.

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11

Northmore, Jennifer Anne, Dustin Sigurdson, Sarah Schoor, Amer Rustum, and Simon D. X. Chuong. "Thidiazuron induces high-frequency indirect shoot organogenesis of Bienertia sinuspersici: a single-cell C4 species." Plant Cell, Tissue and Organ Culture (PCTOC) 126, no. 1 (March 25, 2016): 141–51. http://dx.doi.org/10.1007/s11240-016-0984-7.

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12

Wimmer, Diana, Philipp Bohnhorst, Daniela Impe, Inhwan Hwang, and Sascha Offermann. "Agrobacterium-mediated transient transformation of Bienertia sinuspersici to assay recombinant protein distribution between dimorphic chloroplasts." Plant Cell Reports 38, no. 7 (January 19, 2019): 779–82. http://dx.doi.org/10.1007/s00299-019-02375-4.

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13

Caburatan, L., J. Kim, and J. Park. "Expression Profiles and Post-Translational Modifications of Phosphoenolpyruvate Carboxylase Isozymes of Bienertia sinuspersici during Leaf Development." Russian Journal of Plant Physiology 66, no. 5 (August 22, 2019): 738–47. http://dx.doi.org/10.1134/s1021443719050042.

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14

Offermann, Sascha, Thomas W. Okita, and Gerald E. Edwards. "Resolving the Compartmentation and Function of C4 Photosynthesis in the Single-Cell C4 Species Bienertia sinuspersici." Plant Physiology 155, no. 4 (January 24, 2011): 1612–28. http://dx.doi.org/10.1104/pp.110.170381.

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15

Leisner, Courtney P., Asaph B. Cousins, Sascha Offermann, Thomas W. Okita, and Gerald E. Edwards. "The effects of salinity on photosynthesis and growth of the single-cell C4 species Bienertia sinuspersici (Chenopodiaceae)." Photosynthesis Research 106, no. 3 (September 14, 2010): 201–14. http://dx.doi.org/10.1007/s11120-010-9595-z.

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16

Uzilday, Baris, Rengin Ozgur, Tolga Yalcinkaya, Ismail Turkan, and A. Hediye Sekmen. "Changes in redox regulation during transition from C 3 to single cell C 4 photosynthesis in Bienertia sinuspersici." Journal of Plant Physiology 220 (January 2018): 1–10. http://dx.doi.org/10.1016/j.jplph.2017.10.006.

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17

Rosnow, Josh, Pradeep Yerramsetty, James O. Berry, Thomas W. Okita, and Gerald E. Edwards. "Exploring mechanisms linked to differentiation and function of dimorphic chloroplasts in the single cell C4 species Bienertia sinuspersici." BMC Plant Biology 14, no. 1 (2014): 34. http://dx.doi.org/10.1186/1471-2229-14-34.

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18

Rosnow, Josh, Sascha Offermann, Joonho Park, Thomas W. Okita, Nathan Tarlyn, Amit Dhingra, and Gerald E. Edwards. "In vitro cultures and regeneration of Bienertia sinuspersici (Chenopodiaceae) under increasing concentrations of sodium chloride and carbon dioxide." Plant Cell Reports 30, no. 8 (April 8, 2011): 1541–53. http://dx.doi.org/10.1007/s00299-011-1067-1.

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19

Lung, Shiu-Cheung, and Simon D. X. Chuong. "A Transit Peptide–Like Sorting Signal at the C Terminus Directs the Bienertia sinuspersici Preprotein Receptor Toc159 to the Chloroplast Outer Membrane." Plant Cell 24, no. 4 (April 2012): 1560–78. http://dx.doi.org/10.1105/tpc.112.096248.

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20

Park, Joonho, Michael Knoblauch, Thomas W. Okita, and Gerald E. Edwards. "Structural changes in the vacuole and cytoskeleton are key to development of the two cytoplasmic domains supporting single-cell C4 photosynthesis in Bienertia sinuspersici." Planta 229, no. 2 (October 30, 2008): 369–82. http://dx.doi.org/10.1007/s00425-008-0836-8.

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21

Akhani, Hossein, João Barroca, Nuria Koteeva, Elena Voznesenskaya, Vincent Franceschi, Gerald Edwards, Seyed Mahmood Ghaffari, and Hubert Ziegler. "Bienertia sinuspersici (Chenopodiaceae): A New Species from Southwest Asia and Discovery of a Third Terrestrial C₄ Plant Without Kranz Anatomy." Systematic Botany 30, no. 2 (April 1, 2005): 290–301. http://dx.doi.org/10.1600/0363644054223684.

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22

Lara, María Valeria, Sascha Offermann, Monica Smith, Thomas W. Okita, Carlos Santiago Andreo, and Gerald E. Edwards. "Leaf Development in the Single-Cell C4 System in Bienertia sinuspersici: Expression of Genes and Peptide Levels for C4 Metabolism in Relation to Chlorenchyma Structure under Different Light Conditions." Plant Physiology 148, no. 1 (July 30, 2008): 593–610. http://dx.doi.org/10.1104/pp.108.124008.

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23

Smith, Monica E., Nouria K. Koteyeva, Elena V. Voznesenskaya, Thomas W. Okita, and Gerald E. Edwards. "Photosynthetic features of non-Kranz type C4 versus Kranz type C4 and C3 species in subfamily Suaedoideae (Chenopodiaceae)." Functional Plant Biology 36, no. 9 (2009): 770. http://dx.doi.org/10.1071/fp09120.

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The objective of this study was to characterise photosynthesis in terrestrial non-Kranz (NK) C4 species, Bienertia sinuspersici Akhani and Suaeda aralocaspica (Bunge) Freitag & Schütze (formerly Borszczowia aralocaspica), compared with closely related Kranz type C4 Suaeda eltonica Iljin and Suaeda taxifolia Standley, and C3 species Suaeda heterophylla Bunge and Suaeda maritima Dumort in subfamily Suaedoideae (Chenopodiaceae). Traditional Kranz type C4 photosynthesis has several advantages over C3 photosynthesis under certain environmental conditions by suppressing photorespiration. The different photosynthetic types were evaluated under varying levels of CO2 and light at 25°C. Both NK and Kranz type species had C4 type CO2 compensation points (corrected for dark-type respiration) and half maximum saturation of photosynthesis at similar levels of atmospheric CO2 (average of 145 µbar for the C4 species v. 330 µbar CO2 for C3 species) characteristic of C4 photosynthesis. CO2 saturated rates of photosynthesis per unit chlorophyll was higher in the C3 (at ~2.5 current ambient CO2 levels) than the C4 species, which is likely related to their higher Rubisco content. The amount of Rubisco as a percentage of total protein was similar in NK and Kranz type species (mean 10.2%), but much lower than in the C3 species (35%). Light saturated rates of CO2 fixation per unit leaf area at 25°C and 340 µbar CO2 were higher in the Kranz species and the NK C4 S. aralocaspica than in the C3 species. In response to light at 340 µbar CO2, there was a difference in rates of photosynthesis per unit Rubisco with NK > Kranz > C3 species. There were no significant differences between the three photosynthetic types in maximum quantum yields, convexity of light response curves, and light compensation points at 25°C. The water use efficiency (CO2 fixed per water transpired) at 340 µbar CO2, 25°C and 1000 µmol quanta m–2 s–1 was on average 3-fold higher in the C4 (NK and Kranz) compared with the C3 species. The results show that the NK species have several C4 traits like the Kranz type species in subfamily Suaedoideae.

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24

Mai, Keith Ka Ki, Wai-Tsun Yeung, Sang-Yun Han, Xiaohao Cai, Inhwan Hwang, and Byung-Ho Kang. "Electron Tomography Analysis of Thylakoid Assembly and Fission in Chloroplasts of a Single-Cell C4 plant, Bienertia sinuspersici." Scientific Reports 9, no. 1 (December 2019). http://dx.doi.org/10.1038/s41598-019-56083-w.

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AbstractBienertia sinuspersici is a single-cell C4 plant species of which chlorenchyma cells have two distinct groups of chloroplasts spatially segregated in the cytoplasm. The central vacuole encloses most chloroplasts at the cell center and confines the rest of the chloroplasts near the plasma membrane. Young chlorenchyma cells, however, do not have large vacuoles and their chloroplasts are homogenous. Therefore, maturing Bienertia chlorenchyma cells provide a unique opportunity to investigate chloroplast proliferation in the central cluster and the remodeling of chloroplasts that have been displaced by the vacuole to the cell periphery. Chloroplast numbers and sizes increased, more notably, during later stages of maturation than the early stages. Electron tomography analyses indicated that chloroplast enlargement is sustained by thylakoid growth and that invaginations from the inner envelope membrane contributed to thylakoid assembly. Grana stacks acquired more layers, differentiating them from stroma thylakoids as central chloroplasts matured. In peripheral chloroplasts, however, grana stacks stretched out to a degree that the distinction between grana stacks and stroma thylakoids was obscured. In central chloroplasts undergoing division, thylakoids inside the cleavage furrow were kinked and severed. Grana stacks in the division zone were disrupted, and large complexes in their membranes were dislocated, suggesting the existence of a thylakoid fission machinery.

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25

Lung, Shiu-Cheung, Matthew D. Smith, J. Kyle Weston, William Gwynne, Nathan Secord, and Simon D. X. Chuong. "The C-terminus of Bienertia sinuspersici Toc159 contains essential elements for its targeting and anchorage to the chloroplast outer membrane." Frontiers in Plant Science 5 (December 23, 2014). http://dx.doi.org/10.3389/fpls.2014.00722.

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26

Wimmer, Diana, Philipp Bohnhorst, Vinay Shekhar, Inhwan Hwang, and Sascha Offermann. "Transit peptide elements mediate selective protein targeting to two different types of chloroplasts in the single-cell C4 species Bienertia sinuspersici." Scientific Reports 7, no. 1 (January 23, 2017). http://dx.doi.org/10.1038/srep41187.

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27

Minges, Alexander, Dominik Janßen, Sascha Offermann, and Georg Groth. "Efficient In Vivo Screening Method for the Identification of C4 Photosynthesis Inhibitors Based on Cell Suspensions of the Single-Cell C4 Plant Bienertia sinuspersici." Frontiers in Plant Science 10 (October 30, 2019). http://dx.doi.org/10.3389/fpls.2019.01350.

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