Genetic evidence for functions of Chloroplast CA in Pyropia yezoensis: decreased CCM but increased starch accumulation

Baoyu Zhang, Xueying Liu, Xiujun Xie, Li Huan, Zhizhuo Shao, Zhiyan Du, Guangce Wang

Advanced Biotechnology ›› 2024, Vol. 2 ›› Issue (2) : 0. DOI: 10.1007/s44307-024-00019-7
Article

Genetic evidence for functions of Chloroplast CA in Pyropia yezoensis: decreased CCM but increased starch accumulation

Author information +
History +

Abstract

In response to the changing intertidal environment, intertidal macroalgae have evolved complicated Ci utilization mechanisms. However, our knowledge regarding the CO2 concentrating mechanism (CCM) of macroalgae is limited. Carbonic anhydrase (CA), a key component of CCM, plays essential roles in many physiological reactions in various organisms. While many genes encode CA in the Pyropia yezoensis genome, the exact function of specific CA in P. yezoensis remains elusive. To explore the particular function of chloroplast CA in intertidal macroalgae, we produced chloroplast-localized βCA1 knockdown mutants of P. yezoensis through RNA interference, and Pyβca1i mutants (hereinafter referred to as ca1i) showed a notable decrease in leaf area and overall biomass, as well as decreased soluble protein and unsaturated fatty acid content under different DIC conditions. However, ca1i mutants showed relatively higher starch content compared to the wild-type. The activity of enzymes involved in the Calvin cycle, photorespiration, Pentose-phosphate pathway, and floridean starch synthesis of P. yezoensis indicated an effective starch accumulation pathway after the interference of βCA1. All results suggest that the decreased activity of PyβCA1 impaired the CCM and development of thalli of P. yezoensis, but stimulated starch accumulation in the cytoplasm through feedback to the photorespiration pathway and pentose phosphate pathway to replenish intermediates for the Calvin cycle. This study is the first to explore the specific function of chloroplast CA in intertidal macroalgae using genomic technology. The results provide valuable insights into the adaption mechanisms of intertidal macroalgae to their environment.

Keywords

Chloroplastic carbonic anhydrase / Photorespiration / RNA interference / Starch accumulation / Pyropia yezoensis

Cite this article

Download citation ▾
Baoyu Zhang, Xueying Liu, Xiujun Xie, Li Huan, Zhizhuo Shao, Zhiyan Du, Guangce Wang. Genetic evidence for functions of Chloroplast CA in Pyropia yezoensis: decreased CCM but increased starch accumulation. Advanced Biotechnology, 2024, 2(2): 0 https://doi.org/10.1007/s44307-024-00019-7

References

[]
Adler L, Díaz-Ramos A, Mao Y, Pukacz KR, Fei C, McCormick AJ. New horizons for building pyrenoid-based CO2-concentrating mechanisms in plants to improve yields. Plant Physiol., 2022, 190(3): 1609-1627, pmcid: 9614477
CrossRef Pubmed Google scholar
[]
Badger MR, Price GD. The Role of Carbonic anhydrase in photosynthesis. Annu Rev Plant Physiol Plant Mol Biol, 1994, 45: 369-392,
CrossRef Google scholar
[]
Bates PD, Jewell JB, Browse J. Rapid separation of developing Arabidopsis seeds from siliques for RNA or metabolite analysis. Plant Methods, 2013, 9: 9, pmcid: 3635905
CrossRef Pubmed Google scholar
[]
Bauwe H, Chollet R. Kinetic Properties of Phosphoenolpyruvate Carboxylase from C3, C4, and C3–C4 Intermediate Species of Flaveria (Asteraceae). Plant Physiol, 1986, 82(3): 695-699, pmcid: 1056191
CrossRef Pubmed Google scholar
[]
Blouin N, Calder BL, Perkins B, Brauley SH. Sensory and fatty acid analysis of two Atalantic species of Porphyra (Rhodophyta). J Appl Phycol, 2006, 18: 79-85,
CrossRef Google scholar
[]
Brawley SH, Blouin NA, Ficko-Blean E, et al.. Insights into the red algae and eukaryotic evolution from the genome of Porphyra umbilicalis (Bangiophyceae, Rhodophyta). Proc Natl Acad Sci USA, 2017, 114(31): E6361-E6370, pmcid: 5547612
CrossRef Pubmed Google scholar
[]
Chen H, Chu J, Chen J, Luo Q, Wang H, et al.. Insights into the ancient adaptation to intertidal environments by red algae based on a genomic and multiomics investigation of Neoporphyra haitanensis. Mol. Biol. Evol., 2022, 39(1): msab315,
CrossRef Pubmed Google scholar
[]
Crawford JD, Cousins AB. Limitation of C4 photosynthesis by low carbonic anhydrase activity increases with temperature but does not influence mesophyll CO2 conductance. J Exp Bot, 2022, 73(3): 927-938,
CrossRef Pubmed Google scholar
[]
FAO. 2019. FAO Yearbook of Fishery and Aquaculture Statistics. http://www.fao.org/fishery/static/Yearbook/YB2017_USBcard/index.htm.
[]
Fernández PA, Roleda MY, Rautenberger R, Hurd CL. Carbonic anhydrase activity in seaweeds: overview and recommendations for measuring activity with an electrometric method, using Macrocystis pyrifera as a model species. Mar. Biol., 2018, 165(5): 88,
CrossRef Google scholar
[]
Fleurence J. Seaweed proteins: biochemical, nutritional aspects and potential uses. Trends in Food Technol, 1999, 10: 25-28,
CrossRef Google scholar
[]
Flügel F, Timm S, Arrivault S, Florian A, Stitt M, et al.. The photorespiratory metabolite 2-Phosphoglycolate regulates photosynthesis and starch accumulation in Arabidopsis. The Plant Cell., 2017, 29(10): 2537-51, pmcid: 5774572
CrossRef Pubmed Google scholar
[]
Fünfgeld MMFF, Wang W, Ishihara H, Arrivault S, Feil R, Smith AM, Stitt M, et al.. Sucrose synthases are not involved in starch synthesis in Arabidopsis leaves. Nature Plants, 2022, 8: 574-582, pmcid: 9122829
CrossRef Pubmed Google scholar
[]
Gee CW, Niyogi KK. The carbonic anhydrase CAH1 is an essential component of the carbon-concentrating mechanism in Nannochloropsis oceanica. Proc Natl Acad Sci USA, 2017, 114: 4537-4542, pmcid: 5410810
CrossRef Pubmed Google scholar
[]
Hines KM, Chaudhari V, Edgeworth KN, Owens TG, Hanson MR. Absence of carbonic anhydrase in chloroplasts affects C3 plant development but not photosynthesis. Proc Natl Acad Sci USA, 2021, 118, pmcid: 8379964
CrossRef Pubmed Google scholar
[]
Hirata R, Uji T, Fukuda S, Mizuta H, Fujiyama A, Tabata S, Saga N. Development of a nuclear transformation system with a codon-optimized selection marker and reporter genes in Pyropia yezoensis (Rhodophyta). J Appl Phycol. 2014;26:1863–68.
[]
Huan L, Wang C, Gao S, He L, Lu X, Wang X, Liu X, Wang G. Preliminary comparison of atmospheric CO2 enhancement to photosynthesis of Pyropia yezoensis (Bangiales, Rhodophyta) leafy thalli and filamentous thalli: Carbon uptake after CO2 enhancement. Phycol Res, 2018, 66: 117-126,
CrossRef Google scholar
[]
Ignatova L, Rudenko N, Zhurikova E, Borisova-Mubaraksh M, Ivanov B. Carbonic anhydrases in photosynthesizing cells of C3 higher plants. Metabolites., 2019, 9(4): 73, pmcid: 6523093
CrossRef Pubmed Google scholar
[]
Karlsson J. A novel alpha -type carbonic anhydrase associated with the thylakoid membrane in Chlamydomonas reinhardtii is required for growth at ambient CO2. EMBO J, 1998, 17: 1208-1216, pmcid: 1170469
CrossRef Pubmed Google scholar
[]
Levey M, Timm S, Metler-Altmann T, Luca Borghi G, Koczor M, Arrivault S, Pm Weber A, Bauwe H, Gowik U, Westhoff P. Efficient 2-phosphoglycolate degradation is required to maintain carbon assimilation and allocation in the C4 plant Flaveria bidentis. J Exp Bot, 2019, 70: 575-587,
CrossRef Pubmed Google scholar
[]
Mackinder LCM, Chen C, Leib RD, Patena W, Blum SR, Rodman M, Ramundo S, Adams CM, Jonikas MC. A spatial interactome reveals the protein organization of the algal CO2-concentrating mechanism. Cell, 2017, 171(133–47)
[]
Markelova AG, Sinetova MP, Kupriyanova EV, Pronina NA. Distribution and functional role of carbonic anhydrase Cah3 associated with thylakoid membranes in the chloroplast and pyrenoid of Chlamydomonas reinhardtii. Russ J Plant Physiol, 2009, 56: 761-768,
CrossRef Google scholar
[]
Martinez-Garcia M, van der Maarel MJEC. Floridoside production by the red microalga Galdieria sulphuraria under different conditions of growth and osmotic stress. AMB Express, 2016, 6(1): 71, pmcid: 5020028
CrossRef Pubmed Google scholar
[]
Millero FJ, Zhang JZ, Lee K, Campbell DM. Titration alkalinity of seawater. Marine Chemistry. 1993;44:153–65.
[]
Moroney JV, Bartlett SG, Samuelsson G. Carbonic anhydrases in plants and algae. Plant, Cell and Environ, 2001, 2: 141-153,
CrossRef Google scholar
[]
Moulin P, Andría JR, Axelsson L, Mercado JM. Different mechanisms of inorganic carbon acquisition in red macroalgae (Rhodophyta) revealed by the use of TRIS buffer. Aquatc Bot., 2011, 95(1): 31-8,
CrossRef Google scholar
[]
Nikolau BJ, Ohlrogge JB, Wurtele ES. . Plant Biotin-Containing Carboxylases Arch Biochem Biophy, 2003, 414: 211-222,
CrossRef Google scholar
[]
Noda H. Health benefits and nutritional properties of nori. J Appl Phycol, 1993, 5: 255-258,
CrossRef Google scholar
[]
Patron NJ, Keeling PJ. Common evolutionary origin of starch biosynthetic enzymes in green and red algae. J Phycol, 2005, 41(6): 1131-1141,
CrossRef Google scholar
[]
Pierrot D, Lewis E, Wallace DWR. MS Excel Program Developed for CO2 System Calculations. ORNL/CDIAC−105a. (Carbon Dioxide Information Analysis Center, Oak Ridge National Laboratory, US Department of Energy, Oak Ridge, Tennessee, 2006)
[]
Raven JA. Photosynthetic and non-photosynthetic roles of carbonic anhydrase in algae and cyanobacteria. Phycologia., 1995, 34(2): 93-101,
CrossRef Google scholar
[]
Rioux L-E, Turgeon SL. Tiwari B, Troy D. Seaweed carbohydrates. Seaweed sustainability: food and non-food applications, 2015 Amsterdam Elsevier 141-192,
CrossRef Google scholar
[]
Shao Z, Xie X, Liu X, Zheng Z, Huan L, Zhang B, Wang G. Overexpression of mitochondrial γCAL1 reveal a unique photoprotection mechanism in intertidal resurrection red algae through decreasing photorespiration. Algal Res, 2022, 66: 102766,
CrossRef Google scholar
[]
Viola R, Nyvall P, Pedersén M. The unique features of starch metabolism in red algae. Proc R Soc Lond B, 2001, 268: 1417-1422,
CrossRef Google scholar
[]
Von Caemmerer S, Quinn V, Hancock NC, Price GD, Furbank RT, Ludwig M. Carbonic anhydrase and C4 photosynthesis: a transgenic analysis. Plant Cell Environ, 2004, 6: 697-703,
CrossRef Google scholar
[]
Wang S. Wang S, Pei L, Duan D. The ultrastructure of Porphyra yezoensis. The ultrastructure of common red seaweeds in China, 2004 Ningbo Publishing Press, Zhejiang China 6-9
[]
Wang Y, Stessman FJ, Spalding MH. The CO2 concentrating mechanism and photosynthetic carbon assimilation in limiting: how Chlamydomonas works against the gradient. Plant J, 2015, 82: 429-448,
CrossRef Pubmed Google scholar
[]
Wang D, Yu X, Xu K, Bi G, Cao M, Zelzion E, Fu C, Sun P, Liu Y, Kong F, et al.. Pyropia yezoensis genome reveals diverse mechanisms of carbon acquisition in the intertidal environment. Nat Commun, 2020, 11: 4028, pmcid: 7423979
CrossRef Pubmed Google scholar
[]
Wei L, Xin Y, Wang Q, Yang J, Hu H, Xu J. RNAi-based targeted gene knockdown in the model oleaginous microalgae Nannochloropsis oceanica. Plant J, 2017, 89: 1236-1250,
CrossRef Pubmed Google scholar
[]
Wei L, El Hajjami M, Shen C, You W, Lu Y, Li J, Jing X, Hu Q, Zhou W, Poetsch A, et al.. Transcriptomic and proteomic responses to very low CO2 suggest multiple carbon concentrating mechanisms in Nannochloropsis oceanica. Biotechnol Biofuels, 2019, 12: 168, pmcid: 6599299
CrossRef Pubmed Google scholar
[]
Wu S, Huang A, Zhang B, Huan L, Zhao P, Lin A, Wang G. Enzyme activity highlights the importance of the oxidative pentose phosphate pathway in lipid accumulation and growth of Phaeodactylum tricornutum under CO2 concentration. Biotechnol Biofuels, 2015, 8: 78, pmcid: 4456714
CrossRef Pubmed Google scholar
[]
Yamano T, Toyokawa C, Shimamura D, Matsuoka T, Fukuzawa H. CO2- dependent migration and relocation of LCIB, a pyrenoid-peripheral protein in chlamydomonas reinhardtii. Plant Physiol, 2021, 188: 1081-1094, pmcid: 8825250
CrossRef Google scholar
[]
Young JN, Rickaby REM, Kapralov MV, Filatov DA. Adaptive signals in algal Rubisco reveal a history of ancient atmospheric carbon dioxide. Philos. Trans. R. Soc. Lond. B Biol. Sci, 2012, 367: 483-92, pmcid: 3248704
CrossRef Pubmed Google scholar
[]
Yu Y, Jia X, Wang W, Jin Y, Liu W, Wang D, Mao Y, Xie C, Liu T. Floridean starch and floridoside metabolic pathways of Neoporphyra haitanensis and their regulatory mechanism under continuous darkness. Mar Drugs, 2021, 19(12): 1-19,
CrossRef Google scholar
[]
Zaffagnini M, Fermani S, Costa A, Lemaire SD, Trost P. Plant cytoplasmic GAPDH: redox post-translational modifications and moonlighting properties. Front Plant Sci, 2013, 4: 450, pmcid: 3824636
CrossRef Pubmed Google scholar
[]
Zeebe RE. On the molecular diffusion coefficients of dissolved CO2, HCO3 , and CO3 2− and their dependence on isotopic mass. Geochim Cosmochim Acta, 2011, 75: 2483-2498,
CrossRef Google scholar
[]
Zhang B, Xie X, Liu X, He L, Sun Y, Wang G. The carbonate concentration mechanism of Pyropia yezoensis (Rhodophyta): evidence from transcriptomics and biochemical data. BMC Plant Biol, 2020, 20: 424, pmcid: 7491142
CrossRef Pubmed Google scholar
[]
Zhang B, Liu X, Huan L, Shao Z, Zheng Z, Wang G. Carbonic anhydrase isoforms of Neopyropia yezoensis: intracellular localization and expression profiles in response to inorganic carbon concentration and life stage. J Phycol, 2022, 58: 657-668,
CrossRef Pubmed Google scholar
[]
Zheng Z, He B, Xie X, Wang G. Co-suppression in Pyropia yezoensis (Rhodophyta) Reveals the Role of PyLHCI in Light Harvesting and Generation Switch. J Phycol, 2021, 57: 160-171,
CrossRef Pubmed Google scholar
[]
Zhou W, He L, Yang F, Lin A, Zhang B, Niu J, Wang G. Pyropia yezoensis can utilize CO2 in the air during moderate dehydration. Chin J Ocean Limnol, 2014, 32: 358-364,
CrossRef Google scholar
[]
Zhurikova EM, Ignatova LK, Rudenko NN, Mudrik VA, Vetoshkina DV, Ivanov BN. The participation of two carbonic anhydrases of alpha family photosynthetic reactions in Arabidopsis thaliana. Biochem Mosc, 2016, 81: 1182-1187,
CrossRef Google scholar
[]
Zou D, Gao K. Photosynthetic bicarbonate utilization in Porphyra haitanensis (Bangiales, Rhodophyta). Chin Sci Bull, 2002, 47: 1629-1633

Accesses

Citations

Detail

Sections
Recommended

/