Skip to main content

MINI REVIEW article

Front. Plant Sci., 17 November 2022
Sec. Plant Physiology
This article is part of the Research Topic Women in Plant Physiology: 2022 View all 11 articles

Physiology of microalgae and their application to sustainable agriculture: A mini-review

  • 1Graduate School of Science and Technology, Niigata University, Niigata, Japan
  • 2Sakeology Center, Niigata University, Niigata, Japan

Concern that depletion of fertilizer feedstocks, which are a finite mineral resource, threatens agricultural sustainability has driven the exploration of sustainable methods of soil fertilization. Given that microalgae, which are unicellular photosynthetic organisms, can take up nutrients efficiently from water systems, their application in a biological wastewater purification system followed by the use of their biomass as a fertilizer alternative has attracted attention. Such applications of microalgae would contribute to the accelerated recycling of nutrients from wastewater to farmland. Many previous reports have provided information on the physiological characteristics of microalgae that support their utility. In this review, we focus on recent achievements of studies on microalgal physiology and relevant applications and outline the prospects for the contribution of microalgae to the establishment of sustainable agricultural practices.

Introduction

With the increasing threat of mineral resource depletion through human activities, demand for renewable feedstocks is rising dramatically. The utilization of photosynthetic organisms, including land plants and algae, offers one promising solution. For example, lignocellulosic biomass, which is composed predominantly of plant secondary cell walls, represents an abundant and renewable feedstock for materials, chemicals, and fuels (Ragauskas et al., 2014; Umezawa, 2018; Miyamoto et al., 2020). Promoting the applications of photosynthetic organisms would contribute to the establishment of a sustainable human society.

In the context of agricultural sustainability, a renewable alternative to synthetic chemical fertilizers is urgently required. Enhanced utilization of synthetic chemical fertilizers in conjunction with the development of modern crop cultivars, in which the yield is highly responsive to intensive fertilization, has contributed to improved crop productivity worldwide (Khush, 2001). For example, in soils a large portion of phosphorus (P), an essential macronutrient for plants, likely exists as non-available or poorly available forms for crops, which increases the importance of P fertilizer. However, because the raw material of P fertilizers, rock phosphate, is a finite resource distributed unevenly in limited areas of the world, depletion of the reserves is of grave concern (Desmidt et al., 2015). In addition, the manufacture of nitrogen (N) fertilizers requires the burning of fossil fuels to fix atmospheric N2 and intensive use of N fertilizers enriches reactive N compounds, leading to soil acidification, water eutrophication, and atmospheric pollution (Hayashi et al., 2021). Thus, to establish a sustainable agricultural system worldwide, renewable alternatives to chemical fertilizers and the adoption of eco-friendly soil fertilization practices (Lin et al., 2019), as well as strategies to increase the nutrient use efficiency of crops (Hu et al., 2015; Wu et al., 2020; Ochiai et al., 2022), should be explored.

Microalgae are unicellular photosynthetic organisms commonly found in freshwater and marine ecosystems. They have been used in both experimental and real-world settings to biologically purify wastewater (Vadiveloo et al., 2021). Wastewater purification systems using microalgae represent a promising alternative to conventional wastewater treatment technologies that consume high amounts of energy, discharge sludge, and emit greenhouse gases (Qiao et al., 2020). Microalgae can rapidly grow and proliferate by efficiently acquiring carbon dioxide (CO2) and nutrients, such as P and N, from water systems (Sukačová et al., 2020). Also, the use of microalgal biomass as a biofertilizer as well as a fuel resource can contribute to the enhanced recycling of nutrients (Das et al., 2019; Khan et al., 2019; Moges et al., 2020).

Previous works have revealed many physiological characteristics favorable to the use of microalgae in sustainable agriculture. In addition, empirical evidence on the effectiveness and characteristics of microalga-based fertilizers associated with their physiology has been reported. This review is focused on interactions between basic and applied studies of microalgae, providing insight into a strategy for the establishment of sustainable agriculture.

Carbon fixation capacity assisted by CO2-concentrating mechanisms

The CO2 assimilation capacity of photosynthetic organisms is critical to their growth. Ribulose 1,5-bisphosphate carboxylase/oxygenase (Rubisco) is a core enzyme involved in carbon fixation reactions. However, Rubisco generally shows a low affinity for CO2 and the carboxylation reaction has a slow catalytic turnover rate. The oxygenase activity of Rubisco is also associated with CO2-consuming photorespiration. These properties of Rubisco limit the efficiency of carbon fixation in photosynthetic organisms. In addition to the properties of Rubisco, aquatic conditions present further challenges for algal carbon fixation because the diffusion of CO2 is substantially slower in water than in air. To overcome these problems, most algae develop CO2-concentrating mechanisms (CCMs) that actively take up and enrich CO2 and HCO3 in the pyrenoid, a chloroplast liquid-like non-membranous compartment rich in Rubisco (Hennacy and Jonikas, 2020). The pyrenoid of the algal model Chlamydomonas reinhardtii is penetrated by pyrenoid tubules, which are cylindrical structures of thylakoid membranes (Engel et al., 2015). The pyrenoid tubules may facilitate the rapid diffusion of small molecules, such as adenosine triphosphate (ATP) and sugars, between the chloroplast stroma and pyrenoid (Engel et al., 2015). A starch sheath composed of multiple starch granules forms around the pyrenoid in response to CO2 limitation (Kuchitsu et al., 1988), which may prevent CO2 diffusion from the pyrenoid.

Earlier reports on C. reinhardtii suggested that flexible CCM systems operate for adaptation to CO2 limitation, i.e., low CO2 (LC; approximately 0.03%–0.5%) and very low CO2 (VLC; < 0.02%) environments (Wang and Spalding, 2014). Under LC conditions, CO2 uptake mechanisms are predominantly activated. It has been suggested that the chloroplast protein limiting CO2 inducible protein B (LCIB), which structurally resembles a β-type carbonic anhydrase (Jin et al., 2016), is indispensable for the stimulation of CO2 uptake under LC conditions (Yamano et al., 2010; Wang and Spalding, 2014). It may be that LCIB captures CO2 leaked from the pyrenoid by unidirectionally hydrating CO2 to HCO3- under LC conditions (Yamano et al., 2022), though recombinant LCIB did not show carbonic anhydrase activity (Jin et al., 2016). LCIB proteins are dispersed uniformly in the chloroplast under LC conditions, whereas they migrate to the pyrenoid periphery under VLC conditions (Yamano et al., 2022). The starch sheath surrounding the pyrenoid is important in the localization of LCIB (Toyokawa et al., 2020). LCIB interacts with its homolog LCIC (Yamano et al., 2010). Additionally, LCIC accumulation is involved in LCIB migration (Yamano et al., 2022). These results suggest that an LCIB–LCIC complex plays a critical role in CCM regulation depending on the CO2 concentration.

Although suppressed under LC conditions, HCO3 uptake is activated under VLC conditions. The ABC transporter high-light activated3 (HLA3) and anion channel LCIA, which are localized in the plasma membrane and chloroplast envelope, respectively, act cooperatively for the HCO3 uptake (Duanmu et al., 2009; Gao et al., 2015; Yamano et al., 2015).

It has been suggested that CCM-assisted carbon fixation is associated with nutrient availability (Raven et al., 2008). For example, a study using C. reinhardtii, Chlamydomonas acidophila, Chlamydomonas pitschmannii, and Scenedesmus vacuolatus observed different impacts of P limitation on their CCM, such as reduction of CO2 and HCO3 uptake (Lachmann et al., 2017). Such impacts might be attributed to energy-demanding processes driven by ATP in the CCMs (Su, 2021). Therefore, P uptake capacity is also crucial for the growth performance of microalgae in water systems. In addition, the P content of microalgal biomass may directly affect its effectiveness as a fertilizer, which will be described further below.

Phosphorus accumulation associated with membrane lipid remodeling

Nutrient availability substantially affects microalgal growth and lipid metabolism. Owing to their utility for lipid production, interactions between nutrient acquisition and lipid metabolism in microalgae have been extensively studied (Moore et al., 2013; Yaakob et al., 2021). However, for microalgal application in a wastewater purification system followed by fertilizer use, the lipid-metabolism-dependent nutrient uptake capacity of microalgae is of greater interest.

P starvation induces membrane lipid remodeling from phospholipids (e.g., phosphatidylethanolamine, phosphatidylcholine, and phosphatidylglycerol) to non-P-containing glycolipids (e.g., sulfoquinovosyldiacylglycerol, SQDG) and/or betaine lipids (e.g., diacylglyceroltrimethylhomoserine, DGTS), thus facilitating P reallocation to other biochemical and cellular processes (Moseley and Grossman, 2009; Rouached et al., 2010). In Nannochloropsis oceanica, the breakdown of phospholipids and the synthesis of DGTS and SQDG are stimulated in the exponential growth phase under P limitation (Mühlroth et al., 2017). Additionally, acyl-editing-mediated conversion of phospholipids to non-P-containing lipids is upregulated in the stationary growth phase (Mühlroth et al., 2017).

The lipid-remodeling-associated P uptake capacity is different in taxonomically diverse microalgae. For example, high P uptake occurs in Nannochloropsis gaditana, Tetraselmis suecica, and Picochlorum atomus, which can actively counterbalance phospholipids with betaine (non-P-containing) lipids under P limitation (Cañavate et al., 2017a; Cañavate et al., 2017b). Meanwhile, such high P uptake is practically absent in Rhodomonas baltica, Chroomonas placoidea, and Chaetoceros gracilis, which constitutively produce betaine lipids with fluctuating abundances of phospholipids depending on P supply levels (Cañavate et al., 2017a; Cañavate et al., 2017b). The diversity may be associated with distinct strategies of microalgae for adaptation to P limitation. Microalgal species displaying a high capacity for P uptake might be useful for the applications in P recycling from wastewater to farmland.

Given that P limitation induces membrane lipid remodeling also in land plants (Nakamura, 2013; Tawaraya et al., 2018; Hayes et al., 2022), information on the molecular mechanisms involved in microalgal lipid remodeling may be beneficial to enhance our understanding of low-P adaptation in land plants. The MYB transcription factor phosphorus starvation response1 (PSR1), a homolog of Arabidopsis thaliana phosphate starvation response regulator1 (PHR1), acts as a crucial regulator of the acquisition and reallocation of P in C. reinhardtii (Shimogawara et al., 1999; Wykoff et al., 1999; Bajhaiya et al., 2016). In a N. oceanica mutant deficient in the gene encoding PSR1, low-P-induced replacement of phospholipids with DGTS and SQDG is not observed (Murakami et al., 2020), further supporting the association of PSR1 with low-P-induced membrane lipid remodeling in microalgal species. In addition, the MYB transcription factor lipid remodeling regulator1 (LRL1), a homolog of AtMYB65 from A. thaliana, upregulates the expression of the gene encoding sulfoquinovosyl diacylglycerol2 (SQD2) involved in SQDG biosynthesis at an advanced stage of the low-P response of C. reinhardtii (Hidayati et al., 2019).

Applications of microalgae for nutrient recycling

Given the aforementioned physiological characteristics that support biomass productivity and nutrient uptake capacity, microalgae are a viable renewable and eco-friendly alternative for conventional wastewater treatment systems (Table 1). For example, Chlorella vulgaris and Microcystis sp. can recover 33 mg P L-1 (79%) and 37 mg P L-1 (88%), respectively, from an initial concentration of 41 mg P L−1 in wastewater in 14 days (Chu et al., 2021). With the escalation in the flow of P from terrestrial to water systems with increased industrialization (Liu et al., 2008; Schlesinger, 2012; Van Dijk et al., 2016), P recovery from wastewaters has become a mandatory practice (Peng et al., 2018). A large amount of P has been recovered annually from wastewater using microalgal biofilm techniques (Sukačová et al., 2020).

TABLE 1
www.frontiersin.org

Table 1 Biomass productivity and nutrient uptake capacity of microalgae in aquatic systems.

Further utilization of microalgal biomass recovered from wastewater treatment systems may facilitate the establishment of nutrient recycling (Table 2). The application of dried microalgal biomass can significantly increase total or plant-available nutrients (Dineshkumar et al., 2018; Dineshkumar et al., 2019; Saadaoui et al., 2019; Sharma et al., 2021) and organic carbon (Renuka et al., 2017) in soils. Deoiled dry biomass, which can be obtained as a residue of microalga-based oil production, improves crop productivity when used as a partial substitute for chemical fertilizers (Silambarasan et al., 2021). There are also reports on the positive effects of microalgal extracts and hydrolysates as a seed primer, foliar spray, and liquid fertilizer (Plaza et al., 2018; Kholssi et al., 2019; Supraja et al., 2020; Kusvuran, 2021). Interestingly, the potential of living microalgae to alleviate saline–alkaline stresses (Ma et al., 2022) and that of a soil-surface biofilm to suppress N loss through NH3 volatilization (de Siqueira Castro et al., 2017) have been reported. Circular economy projects using microalgae for wastewater purification and farmland fertilization in a cattle farm (Lorentz et al., 2020) and winery company (Avila et al., 2022) have been tested.

TABLE 2
www.frontiersin.org

Table 2 Effects of microalga-based fertilizers on agricultural crops.

It has also been reported that algal–bacterial aerobic granular sludge removes greater amounts of P and N from wastewater than does bacteria alone (Wang et al., 2021). Bacterial degradation of organic carbon may mitigate the issue of microalgal CO2 acquisition in water systems, which was mentioned above. Additionally, the artificial augmentation of CO2 in wastewater via supplementation with flue gas from combustion may also stimulate microalgal biomass productivity and nutrient uptake capacity, potentially resulting in enhanced nutrient recycling (He et al., 2012; Lara-Gil et al., 2016; Yadav et al., 2019).

Characteristics of microalga-based fertilizers

The application of dry biomass from Chlorella minutissima reduced the leaching of nitrate from farmland and increased leaf N content of spinach (Spinacia oleracea) plants (Sharma et al., 2022) (Table 2). The application of Asterarcys quadricellulare extracts significantly stimulated N assimilation and the nitrate reductase activity of potato (Solanum tuberosum) plants (Cordeiro et al., 2022). The applications of C. vulgaris biomass and chemical fertilizer resulted in comparable levels of shoot N uptake in wheat (Triticum aestivum) plants (Schreiber et al., 2018). These results demonstrate the effectiveness of the microalga-based fertilizer. However, the level of shoot P uptake was lower in the wheat plants grown under the microalgal treatment than in those grown under the chemical fertilizer treatment (Schreiber et al., 2018), suggesting that microalgal biomass acts as a slow-release P fertilizer. Microalgae can store P as polyphosphates (Delgadillo-Mirquez et al., 2016; Solovchenko et al., 2019; Chu et al., 2021), which are degraded slowly by soil microbes (Powell et al., 2011; Ray et al., 2013; Solovchenko et al., 2019). Furthermore, hydrothermal carbonization of microalgal biomass enhances its characteristics as a slow-release fertilizer, which increases the amount of moderately available P in soils more persistently compared with chemical fertilizer (Chu et al., 2021) (Table 2). Such fertilizer characteristics might increase the nutrient use efficiency of crops and/or reduce environmental pollution by suppressing the leaching of nutrients from farmland (Coppens et al., 2016; Jimenez et al., 2020; Sharma et al., 2022).

The application of microalgal extracts enriches essential macronutrients such as P, potassium, calcium, and magnesium in tomato plants (Suchithra et al., 2022) (Table 2). Microalga-based fertilizers also supply essential micronutrients as well as beneficial elements for plants (de Haes et al., 2012; Maurya et al., 2016; Wuang et al., 2016; Silva et al., 2019). In a wheat cultivation test, the application of microalgal biomass increased the contents of zinc, iron, copper, and manganese in plants (Rana et al., 2012; Prasanna et al., 2013; Renuka et al., 2017). Microalgal biomass rich in selenium, a beneficial element for plants, has been also suggested to serve as an effective fertilizer (Han et al., 2020).

Garcia-Gonzalez and Sommerfeld (2016) and Deepika and MubarakAli (2020) mentioned the occurrence in microalgal extracts of phytohormones that upregulate plant growth. It has been considered that microalgal components, including phytohormones, stimulate the production of antifungal substances in plants (Spolaore et al., 2006; Coppens et al., 2016). In addition, crude polysaccharides obtained from microalgae have a biostimulant-like effect on plants (Farid et al., 2019; Rachidi et al., 2020) (Table 2). Plant morphological traits, such as plant height, leaf number, tillering rate, root length, and lateral root number, are positively affected by the application of a microalga-based fertilizer depending on its dosage (Wuang et al., 2016; Nayak et al., 2019; Deepika and MubarakAli, 2020) (Table 2). Commercially important components of fruit, such as carotenoids and sugars, increase in response to the application of microalga-based fertilizers (Kumari et al., 2011; Coppens et al., 2016; Mutale-Joan et al., 2020; Cordeiro et al., 2022). These changes might be partially due to the effect of plant growth regulators in microalgal biomass, although further investigation is required for verification.

Conclusions and prospects

To achieve rapid growth and efficient nutrient accumulation in water systems, microalgae developed mechanisms such as flexible CCMs and membrane lipid remodeling. Previous research has shed light on the sophisticated molecular interactions underlying the physiological characteristics of microalgae, which support its utility as a wastewater purification system and fertilizer. Applications of microalgae in a wastewater purification system followed by fertilizer use may facilitate the establishment of nutrient recycling. Many studies have shown that application of microalgal biomass can provide nutrients essential for plants and enrich organic carbons in soils. In addition, microalgal biomass contains slowly degradable forms of plant-essential nutrients, reducing the leaching of the nutrients from farmland. Furthermore, microalga-based fertilizers are regarded as suppliers of plant growth regulators. However, challenges remain in the expansion of microalga-based technologies. For example, a life cycle assessment highlighted the detrimental impact of electricity consumption required for microalgal cultivation (Diniz et al., 2017; de Souza et al., 2019). In addition, the application of a microalga-based fertilizer can stimulate the emission of greenhouse gases, such as N2O and CO2, from soils (Suleiman et al., 2020). Thus, further technological advances, as well as a more in-depth understanding of microalgal physiology, are required for wider implementation of microalgal applications for sustainable agriculture.

Author contributions

IC, TM, and NO wrote the manuscript. All authors contributed to the article and approved the submitted version.

Funding

This work was partially supported by the Japan Society for the Promotion of Science (JSPS) KAKENHI grant (JP#22K14876).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

Avila, R., Justo, Á., Carrero, E., Crivillés, E., Vicent, T., Blánquez, P. (2022). Water resource recovery coupling microalgae wastewater treatment and sludge co-digestion for bio-wastes valorisation at industrial pilot-scale. Bioresorce Technol. 343, 126080. doi: 10.1016/j.biortech.2021.126080

CrossRef Full Text | Google Scholar

Bajhaiya, A. K., Dean, A. P., Zeef, L. A. H., Webster, R. E., Pittman, J. K. (2016). PSR1 is a global transcriptional regulator of phosphorus deficiency responses and carbon storage metabolism in Chlamydomonas reinhardtii. Plant Physiol. 170 (3), 1216–1234. doi: 10.1104/pp.15.01907

PubMed Abstract | CrossRef Full Text | Google Scholar

Cañavate, J. P., Armada, I., Hachero-Cruzado, I. (2017a). Aspects of phosphorus physiology associated with phosphate-induced polar lipid remodelling in marine microalgae. J. Plant Physiol. 214, 28–38. doi: 10.1016/j.jplph.2017.03.019

PubMed Abstract | CrossRef Full Text | Google Scholar

Cañavate, J. P., Armada, I., Hachero-Cruzado, I. (2017b). Interspecific variability in phosphorus-induced lipid remodelling among marine eukaryotic phytoplankton. New Phytol. 213 (2), 700–713. doi: 10.1111/nph.14179

PubMed Abstract | CrossRef Full Text | Google Scholar

Chu, Q., Lyu, T., Xue, L., Yang, L., Feng, Y., Sha, Z., et al. (2021). Hydrothermal carbonization of microalgae for phosphorus recycling from wastewater to crop-soil systems as slow-release fertilizers. J. Clean. Prod. 283, 124627. doi: 10.1016/j.jclepro.2020.124627

CrossRef Full Text | Google Scholar

Coppens, J., Grunert, O., Van Den Hende, S., Vanhoutte, I., Boon, N., Haesaert, G., et al. (2016). The use of microalgae as a high-value organic slow-release fertilizer results in tomatoes with increased carotenoid and sugar levels. J. Appl. Phycol. 28 (4), 2367–2377. doi: 10.1007/s10811-015-0775-2

CrossRef Full Text | Google Scholar

Cordeiro, E. C. N., Mógor, Á.F., Amatussi, J. O., Mógor, G., Marques, H. M. C., de Lara, G. B. (2022). Microalga biofertilizer improves potato growth and yield, stimulating amino acid metabolism. J. Appl. Phycol. 34 (1), 385–394. doi: 10.1007/s10811-021-02656-0

CrossRef Full Text | Google Scholar

Das, P., Quadir, M. A., Thaher, M. I., Alghasal, G. S. H. S., Aljabri, H. M. S. J. (2019). Microalgal nutrients recycling from the primary effluent of municipal wastewater and use of the produced biomass as bio-fertilizer. Int. J. Environ. Sci. Technol. 16 (7), 3355–3364. doi: 10.1007/s13762-018-1867-8

CrossRef Full Text | Google Scholar

Deepika, P., MubarakAli, D. (2020). Production and assessment of microalgal liquid fertilizer for the enhanced growth of four crop plants. Biocatal. Agric. Biotechnol. 28 (1), 101701. doi: 10.1016/j.bcab.2020.101701

CrossRef Full Text | Google Scholar

de Haes, H. A. U., Voortman, R. L., Bastein, T., Bussink, D. W., Rougoor, C. W., van der Weijden, W. J. (2012) Scarcity of micronutrients in soil, food and mineral reserves -urgency and policy options-. platform agriculture, innovation and society. Available at: https://www.iatp.org/sites/default/files/scarcity_of_micronutrients.pdf.

Google Scholar

Delgadillo-Mirquez, L., Lopes, F., Taidi, B., Pareau, D. (2016). Nitrogen and phosphate removal from wastewater with a mixed microalgae and bacteria culture. Biotechnol. Rep. 11, 18–26. doi: 10.1016/j.btre.2016.04.003

CrossRef Full Text | Google Scholar

de Siqueira Castro, J., Calijuri, M. L., Assemany, P. P., Cecon, P. R., de Assis, I. R., Ribeiro, V. J. (2017). Microalgae biofilm in soil: Greenhouse gas emissions, ammonia volatilization and plant growth. Sci. Total Environ. 574, 1640–1648. doi: 10.1016/j.scitotenv.2016.08.205

PubMed Abstract | CrossRef Full Text | Google Scholar

Desmidt, E., Ghyselbrecht, K., Zhang, Y., Pinoy, L., van der Bruggen, B., Verstraete, W., et al. (2015). Global phosphorus scarcity and full-scale p-recovery techniques: A review. Crit. Rev. Env. Tec. Sci. 45 (4), 336–384. doi: 10.1080/10643389.2013.866531

CrossRef Full Text | Google Scholar

de Souza, M. H. B., Calijuri, M. L., Assemany, P. P., de Siqueira Castro, J., de Oliveira, A. C. M. (2019). Soil application of microalgae for nitrogen recovery: A life-cycle approach. J. Clean. Prod. 211, 342–349. doi: 10.1016/j.jclepro.2018.11.097

CrossRef Full Text | Google Scholar

Dineshkumar, R., Kumaravel, R., Gopalsamy, J., Sikder, M. N. A., Sampathkumar, P. (2018). Microalgae as bio-fertilizers for rice growth and seed yield productivity. Waste Biomass Valor. 9 (5), 793–800. doi: 10.1007/s12649-017-9873-5

CrossRef Full Text | Google Scholar

Dineshkumar, R., Subramanian, J., Gopalsamy, J., Jayasingam, P., Arumugam, A., Kannadasan, S., et al. (2019). The impact of using microalgae as biofertilizer in maize (Zea mays l.). Waste Biomass Valor. 10 (5), 1101–1110. doi: 10.1007/s12649-017-0123-7

CrossRef Full Text | Google Scholar

Diniz, G. S., Tourinho, T. C., Silva, A. F., Chaloub, R. M. (2017). Environmental impact of microalgal biomass production using wastewater resources. Clean Technol. Envir. 19 (10), 2521–2529. doi: 10.1007/s10098-017-1433-y

CrossRef Full Text | Google Scholar

Duanmu, D., Miller, A. R., Horken, K. M., Weeks, D. P., Spalding, M. H. (2009). Knockdown of limiting-CO2-induced gene HLA3 decreases HCO3- transport and photosynthetic ci affinity in Chlamydomonas reinhardtii. Proc. Natl. Acad. Sci. U.S.A. 106 (14), 5990–5995. doi: 10.1073/pnas.0812885106

PubMed Abstract | CrossRef Full Text | Google Scholar

Engel, B. D., Schaffer, M., Kuhn Cuellar, L., Villa, E., Plitzko, J. M., Baumeister, W. (2015). Native architecture of the chlamydomonas chloroplast revealed by in situ cryo-electron tomography. eLife 4, e04889. doi: 10.7554/eLife.04889

PubMed Abstract | CrossRef Full Text | Google Scholar

Farid, R., Mutale-Joan, C., Redouane, B., Mernissi Najib, E. L., Abderahime, A., Laila, S., et al. (2019). Effect of microalgae polysaccharides on biochemical and metabolomics pathways related to plant defense in solanum lycopersicum. Appl. Biochem. Biotechnol. 188 (1), 225–240. doi: 10.1007/s12010-018-2916-y

PubMed Abstract | CrossRef Full Text | Google Scholar

Gao, H., Wang, Y., Fei, X., Wright, D. A., Spalding, M. H. (2015). Expression activation and functional analysis of HLA3, a putative inorganic carbon transporter in Chlamydomonas reinhardtii. Plant J. 82 (1), 1–11. doi: 10.1111/tpj.12788

PubMed Abstract | CrossRef Full Text | Google Scholar

Garcia-Gonzalez, J., Sommerfeld, M. (2016). Biofertilizer and biostimulant properties of the microalga acutodesmus dimorphus. J. Appl. Phycol. 28 (2), 1051–1061. doi: 10.1007/s10811-015-0625-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Han, W., Mao, Y., Wei, Y., Shang, P., Zhou, X. (2020). Bioremediation of aquaculture wastewater with algal-bacterial biofilm combined with the production of selenium rich biofertilizer. Water 12 (7), 2071. doi: 10.3390/w12072071

CrossRef Full Text | Google Scholar

Hayashi, K., Shibata, H., Oita, A., Nishina, K., Ito, A., Katagiri, K., et al. (2021). Nitrogen budgets in Japan from 2000 to 2015: Decreasing trend of nitrogen loss to the environment and the challenge to further reduce. Environ. Pollut. 286 (10), 117559. doi: 10.1016/j.envpol.2021.117559

CrossRef Full Text | Google Scholar

Hayes, P. E., Adem, G. D., Pariasca-Tanaka, J., Wissuwa, M. (2022). Leaf phosphorus fractionation in rice to understand internal phosphorus-use efficiency. Ann. Bot. 129 (3), 287–301. doi: 10.1093/aob/mcab138

PubMed Abstract | CrossRef Full Text | Google Scholar

Hennacy, J. H., Jonikas, M. C. (2020). Prospects for engineering biophysical CO2 concentrating mechanisms into land plants to enhance yields. Annu. Rev. Plant Biol. 71, 461–485. doi: 10.1146/annurev-arplant-081519-040100

PubMed Abstract | CrossRef Full Text | Google Scholar

He, L., Subramanian, V. R., Tang, Y. J. (2012). Experimental analysis and model-based optimization of microalgae growth in photo-bioreactors using flue gas. Biomass Bioenerg. 41, 131–138. doi: 10.1016/j.biombioe.2012.02.025

CrossRef Full Text | Google Scholar

Hidayati, N. A., Yamada-Oshima, Y., Iwai, M., Yamano, T., Kajikawa, M., Sakurai, N., et al. (2019). Lipid remodeling regulator 1 (LRL1) is differently involved in the phosphorus-depletion response from PSR1 in Chlamydomonas reinhardtii. Plant J. 100 (3), 610–626. doi: 10.1111/tpj.14473

PubMed Abstract | CrossRef Full Text | Google Scholar

Hu, B., Wang, W., Ou, S., Tang, J., Li, H., Che, R., et al. (2015). Variation in NRT1.1B contributes to nitrate-use divergence between rice subspecies. Nat. Genet. 47 (7), 834–838. doi: 10.1038/ng.3337

PubMed Abstract | CrossRef Full Text | Google Scholar

Jimenez, R., Markou, G., Tayibi, S., Barakat, A., Chapsal, C., Monlau, F. (2020). Production of microalgal slow-release fertilizer by valorizing liquid agricultural digestate: Growth experiments with tomatoes. Appl. Sci. 10 (11), 3890. doi: 10.3390/app10113890

CrossRef Full Text | Google Scholar

Jin, S., Sun, J., Wunder, T., Tang, D., Cousins, A. B., Sze, S. K., et al. (2016). Structural insights into the LCIB protein family reveals a new group of β-carbonic anhydrases. Proc. Natl. Acad. Sci. U.S.A. 113 (51), 14716–14721. doi: 10.1073/pnas.1616294113

PubMed Abstract | CrossRef Full Text | Google Scholar

Khan, S. A., Sharma, G. K., Malla, F. A., Kumar, A. (2019). Microalgae based biofertilizers: A biorefinery approach of phycoremediate wastewater and harvest biodiesel and manure. J. Clean. Prod. 211, 1412–1419. doi: 10.1016/j.jclepro.2018.11.281

CrossRef Full Text | Google Scholar

Kholssi, R., Marks, E. A., Miñón, J., Montero, O., Debdoubi, A., Rad, C. (2019). Biofertilizing effect of chlorella sorokiniana suspensions on wheat growth. J. Plant Growth Regul. 38 (2), 644–649. doi: 10.1007/s00344-018-9879-7

CrossRef Full Text | Google Scholar

Khush, G. S. (2001). Green revolution: The way forward. Nat. Rev. Genet. 2 (10), 815–822. doi: 10.1038/35093585

PubMed Abstract | CrossRef Full Text | Google Scholar

Kuchitsu, K., Tsuzuki, M., Miyachi, S. (1988). Changes of starch localization within the chloroplast induced by changes in CO2 concentration during growth of Chlamydomonas reinhardtii: Independent regulation of pyrenoid starch and stroma starch. Plant Cell Physiol. 29 (8), 1269–1278. doi: 10.1093/oxfordjournals.pcp.a077635

CrossRef Full Text | Google Scholar

Kumari, R., Kaur, I., Bhatnagar, A. K. (2011). Effect of aqueous extract of sargassum johnstonii setchell & Gardner on growth, yield and quality of Lycopersicon esculentum mill. J. Appl. Phycol. 23 (3), 623–633. doi: 10.1007/s10811-011-9651-x

CrossRef Full Text | Google Scholar

Kusvuran, S. (2021). Microalgae (Chlorella vulgaris beijerinck) alleviates drought stress of broccoli plants by improving nutrient uptake, secondary metabolites, and antioxidative defense system. Hortic. Plant J. 7 (3), 221–231. doi: 10.1016/j.hpj.2021.03.007

CrossRef Full Text | Google Scholar

Lachmann, S. C., Maberly, S. C., Spijkerman, E. (2017). Species-specific influence of pi-status on inorganic carbon acquisition in microalgae (Chlorophyceae). Botany 95 (9), 943–952. doi: 10.1139/cjb-2017-0082

CrossRef Full Text | Google Scholar

Lara-Gil, J. A., Senés-Guerrero, C., Pacheco, A. (2016). Cement flue gas as a potential source of nutrients during CO2 mitigation by microalgae. Algal. Res. 17, 285–292. doi: 10.1016/j.algal.2016.05.017

CrossRef Full Text | Google Scholar

Lin, W., Lin, M., Zhou, H., Wu, H., Li, Z., Lin, W. (2019). The effects of chemical and organic fertilizer usage on rhizosphere soil in tea orchards. PloS One 14 (5), e0217018. doi: 10.1371/journal.pone.0217018

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, Y., Villalba, G., Ayres, R. U., Schroder, H. (2008). Global phosphorus flows and environmental impacts from a consumption perspective. J. Ind. Ecol. 12 (2), 229–247. doi: 10.1111/j.1530-9290.2008.00025.x

CrossRef Full Text | Google Scholar

Lorentz, J. F., Calijuri, M. L., Assemany, P. P., Alves, W. S., Pereira, O. G. (2020). Microalgal biomass as a biofertilizer for pasture cultivation: Plant productivity and chemical composition. J. Clean. Prod. 276, 124130. doi: 10.1016/j.jclepro.2020.124130

CrossRef Full Text | Google Scholar

Ma, C., Cui, H., Ren, C., Yang, J., Liu, Z., Tang, T., et al. (2022). The seed primer and biofertilizer performances of living Chlorella pyrenoidosa on Chenopodium quinoa under saline-alkali condition. J. Appl. Phycol. 34 (3), 1621–1634. doi: 10.1007/s10811-022-02699-x

CrossRef Full Text | Google Scholar

Maurya, R., Chokshi, K., Ghosh, T., Trivedi, K., Pancha, I., Kubavat, D., et al. (2016). Lipid extracted microalgal biomass residue as a fertilizer substitute for Zea mays l. Front. Plant Sci. 6. doi: 10.3389/fpls.2015.01266

PubMed Abstract | CrossRef Full Text | Google Scholar

Miyamoto, T., Tobimatsu, Y., Umezawa, T. (2020). MYB-mediated regulation of lignin biosynthesis in grasses. Curr. Plant Biol. 24, 100174. doi: 10.1016/j.cpb.2020.100174

CrossRef Full Text | Google Scholar

Moges, M. E., Heistad, A., Heidorn, T. (2020). Nutrient recovery from anaerobically treated blackwater and improving its effluent quality through microalgae biomass production. Water 12 (2), 592. doi: 10.3390/w12020592

CrossRef Full Text | Google Scholar

Moore, C. M., Mills, M. M., Arrigo, K. R., Berman-Frank, I., Bopp, L., Boyd, P. W., et al. (2013). Processes and patterns of oceanic nutrient limitation. Nat. Geosci. 6 (9), 701–710. doi: 10.1038/ngeo1765

CrossRef Full Text | Google Scholar

Moseley, J. L., Grossman, A. R. (2009). “Phosphorus limitation from the physiological to the genomic,” in The chlamydomonas source-book: Organellar and metabolic processes, vol. 2 . Ed. Stern, D. B. (San Diego: Academic Press), 189–215.

Google Scholar

Mühlroth, A., Winge, P., El Assimi, A., Jouhet, J., Maréchal, E., Hohmann-Marriott, M. F., et al. (2017). Mechanisms of phosphorus acquisition and lipid class remodeling under p limitation in a marine microalga. Plant Physiol. 175 (4), 1543–1559. doi: 10.1104/pp.17.00621

PubMed Abstract | CrossRef Full Text | Google Scholar

Murakami, H., Kakutani, N., Kuroyanagi, Y., Iwai, M., Hori, K., Shimojima, M., et al. (2020). MYB-like transcription factor NoPSR1 is crucial for membrane lipid remodeling under phosphate starvation in the oleaginous microalga. Nannochloropsis oceanica. FEBS Lett. 594 (20), 3384–3394. doi: 10.1002/1873-3468.13902

CrossRef Full Text | Google Scholar

Mutale-Joan, C., Redouane, B., Najib, E., Yassine, K., Lyamlouli, K., Laila, S., et al. (2020). Screening of microalgae liquid extracts for their bio stimulant properties on plant growth, nutrient uptake and metabolite profile of Solanum lycopersicum l. Sci. Rep. 10 (1), 1–12. doi: 10.1038/s41598-020-59840-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Nayak, M., Swain, D. K., Sen, R. (2019). Strategic valorization of de-oiled microalgal biomass waste as biofertilizer for sustainable and improved agriculture of rice (Oryza sativa L.) crop. Sci. Total Environ. 682, 475–484. doi: 10.1016/j.scitotenv.2019.05.123

PubMed Abstract | CrossRef Full Text | Google Scholar

Nakamura, Y. (2013). Phosphate starvation and membrane lipid remodeling in seed plants. Prog. Lipid Res. 52 (1), 43–50. doi: 10.1016/j.plipres.2012.07.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Ochiai, K., Oba, K., Oda, K., Miyamoto, T., Matoh, T. (2022). Effects of improved sodium uptake ability on grain yields of rice plants under low potassium supply. Plant Dir. 6 (4), e384. doi: 10.1002/pld3.387

CrossRef Full Text | Google Scholar

Peng, L., Dai, H., Wu, Y., Peng, Y., Lu, X. A. (2018). Comprehensive review of the available media and approaches for phosphorus recovery from wastewater. Water Air Soil pollut. 229 (4), 1–28. doi: 10.1007/s11270-018-3706-4

CrossRef Full Text | Google Scholar

Plaza, B. M., Gómez-Serrano, C., Acién-Fernández, F. G., Jimenez-Becker, S. (2018). Effect of microalgae hydrolysate foliar application (Arthrospira platensis and Scenedesmus sp.) on petunia x hybrida growth. J. Appl. Phycol. 30 (4), 2359–2365. doi: 10.1007/s10811-018-1427-0

CrossRef Full Text | Google Scholar

Powell, N., Shilton, A., Pratt, S., Chisti, Y. (2011). Phosphate release from waste stabilisation pond sludge: Significance and fate of polyphosphate. Water Sci. Technol. 63 (8), 1689–1694. doi: 10.2166/wst.2011.336

PubMed Abstract | CrossRef Full Text | Google Scholar

Prasanna, R., Babu, S., Rana, A., Kabi, S. R., Chaudhary, V., Gupta, V., et al. (2013). Evaluating the establishment and agronomic proficiency of cyanobacterial consortia as organic options in wheat–rice cropping sequence. Exp. Agric. 49 (3), 416–434. doi: 10.1017/S001447971200107X

CrossRef Full Text | Google Scholar

Qiao, S., Hou, C., Wang, X., Zhou, J. (2020). Minimizing greenhouse gas emission from wastewater treatment process by integrating activated sludge and microalgae processes. Sci. Total Environ. 732 (4), 139032. doi: 10.1016/j.scitotenv.2020.139032

PubMed Abstract | CrossRef Full Text | Google Scholar

Rachidi, F., Benhima, R., Sbabou, L., El Arroussi, H. (2020). Microalgae polysaccharides bio-stimulating effect on tomato plants: Growth and metabolic distribution. Biotechnol. Rep. 25, e00426. doi: 10.1016/j.btre.2020.e00426

CrossRef Full Text | Google Scholar

Ragauskas, A. J., Beckham, G. T., Biddy, M. J., Chandra, R., Chen, F., Davis, M. F., et al. (2014). Lignin valorization: Improving lignin processing in the biorefinery. Science 344 (6185), 1246843. doi: 10.1126/science.1246843

PubMed Abstract | CrossRef Full Text | Google Scholar

Rana, A., Joshi, M., Prasanna, R., Shivay, Y. S., Nain, L. (2012). Biofortification of wheat through inoculation of plant growth promoting rhizobacteria and cyanobacteria. Eur. J. Soil Biol. 50, 118–126. doi: 10.1016/j.ejsobi.2012.01.005

CrossRef Full Text | Google Scholar

Raven, J. A., Cockell, C. S., La Rocha, C. L. (2008). The evolution of inorganic carbon concentrating mechanisms in photosynthesis. Philos. Trans. R. Soc B-Biol. Sci. 363 (1504), 2641–2650. doi: 10.1098/rstb.2008.0020

CrossRef Full Text | Google Scholar

Ray, K., Mukherjee, C., Ghosh, A. N. (2013). A way to curb phosphorus toxicity in the environment: Use of polyphosphate reservoir of cyanobacteria and microalga as a safe alternative phosphorus biofertilizer for Indian agriculture. Environ. Sci. Technol. 47 (20), 11378–11379. doi: 10.1021/es403057c

PubMed Abstract | CrossRef Full Text | Google Scholar

Renuka, N., Prasanna, R., Sood, A., Bansal, R., Bidyarani, N., Singh, R., et al. (2017). Wastewater grown microalgal biomass as inoculants for improving micronutrient availability in wheat. Rhizosphere 3 (2), 150–159. doi: 10.1016/j.rhisph.2017.04.005

CrossRef Full Text | Google Scholar

Rouached, H., Arpat, A. B., Poirier, Y. (2010). Regulation of phosphate starvation responses in plants: Signaling players and cross-talks. Mol. Plant 3 (2), 288–299. doi: 10.1093/mp/ssp120

CrossRef Full Text | Google Scholar

Saadaoui, I., Sedky, R., Rasheed, R., Bounnit, T., Almahmoud, A., Elshekh, A., et al. (2019). Assessment of the algae-based biofertilizer influence on date palm (Phoenix dactylifera l.) cultivation. J. Appl. Phycol. 31 (1), 457–463. doi: 10.1007/s10811-018-1539-6

CrossRef Full Text | Google Scholar

Schlesinger, W. H. (2012). Biogeochemistry: An analysis of global change. 3rd ed (New York, NY, USA: Elsevier/Academic Press).

Google Scholar

Schreiber, C., Schiedung, H., Harrison, L., Briese, C., Ackermann, B., Kant, J., et al. (2018). Evaluating potential of green alga Chlorella vulgaris to accumulate phosphorus and to fertilize nutrient-poor soil substrates for crop plants. J. Appl. Phycol. 30 (5), 2827–2836. doi: 10.1007/s10811-018-1390-9

CrossRef Full Text | Google Scholar

Shaaban, M. M., El-Saady, A. M., El-Sayed, A. B. (2010). Green microalgae water extract and micronutrients foliar application as promoters to nutrient balance and growth of wheat plants. J. Am. Sci. 6 (9), 631–636. doi: 10.3923/pjbs.2001.628.632

CrossRef Full Text | Google Scholar

Sharma, G. K., Khan, S. A., Shrivastava, M., Bhattacharyya, R., Sharma, A., Gupta, D. K., et al. (2021). Circular economy fertilization: Phycoremediated algal biomass as biofertilizers for sustainable crop production. J. Environ. Manage. 287 (4), 112295. doi: 10.1016/j.jenvman.2021.112295

PubMed Abstract | CrossRef Full Text | Google Scholar

Sharma, G. K., Khan, S. A., Shrivastava, M., Bhattacharyya, R., Sharma, A., Gupta, N., et al. (2022). Phycoremediated n-fertilization approaches on reducing environmental impacts of agricultural nitrate leaching. J. Cleaner Production 345 (5), 131120. doi: 10.1016/j.jclepro.2022.131120

CrossRef Full Text | Google Scholar

Shimogawara, K., Wykoff, D. D., Usuda, H., Grossman, A. R. (1999). Chlamydomonas reinhardtii mutants abnormal in their responses to phosphorus deprivation. Plant Physiol. 120 (3), 685–694. doi: 10.1104/pp.120.3.685

PubMed Abstract | CrossRef Full Text | Google Scholar

Silambarasan, S., Logeswari, P., Sivaramakrishnan, R., Incharoensakdi, A., Cornejo, P., Kamaraj, B., et al. (2021). Removal of nutrients from domestic wastewater by microalgae coupled to lipid augmentation for biodiesel production and influence of deoiled algal biomass as biofertilizer for Solanum lycopersicum cultivation. Chemosphere 268 (8), 129323. doi: 10.1016/j.chemosphere.2020.129323

PubMed Abstract | CrossRef Full Text | Google Scholar

Silva, G. H., Sueitt, A. P. E., Haimes, S., Tripidaki, A., van Zwieten, R., Fernandes, T. V. (2019). Feasibility of closing nutrient cycles from black water by microalgae-based technology. Algal. Res. 44 (6), 101715. doi: 10.1016/j.algal.2019.101715

CrossRef Full Text | Google Scholar

Solovchenko, A., Khozin-Goldberg, I., Selyakh, I., Semenova, L., Ismagulova, T., Lukyanov, A., et al. (2019). Phosphorus starvation and luxury uptake in green microalgae revisited. Algal. Res. 43, 101651. doi: 10.1016/j.algal.2019.101651

CrossRef Full Text | Google Scholar

Spolaore, P., Joannis-Cassan, C., Duran, E., Isambert, A. (2006). Commercial applications of microalgae. J. Biosci. Bioeng. 101 (2), 87–96. doi: 10.1263/jbb.101.87

PubMed Abstract | CrossRef Full Text | Google Scholar

Su, Y. (2021). Revisiting carbon, nitrogen, and phosphorus metabolisms in microalgae for wastewater treatment. Sci. Total Environ. 762 (1), 144590. doi: 10.1016/j.scitotenv.2020.144590

PubMed Abstract | CrossRef Full Text | Google Scholar

Suchithra, M. R., Muniswami, D. M., Sri, M. S., Usha, R., Rasheeq, A. A., Preethi, B. A. (2022). Effectiveness of green microalgae as biostimulants and biofertilizer through foliar spray and soil drench method for tomato cultivation. S. Afr. J. Bot. 146 (14), 740–750. doi: 10.1016/j.sajb.2021.12.022

CrossRef Full Text | Google Scholar

Sukačová, K., Vícha, D., Dušek, J. (2020). Perspectives on microalgal biofilm systems with respect to integration into wastewater treatment technologies and phosphorus scarcity. Water 12 (8), 2245. doi: 10.3390/w12082245

CrossRef Full Text | Google Scholar

Suleiman, A. K. A., Lourenço, K. S., Clark, C., Luz, R. L., da Silva, G. H. R., Vet, L. E., et al. (2020). From toilet to agriculture: Fertilization with microalgal biomass from wastewater impacts the soil and rhizosphere active microbiomes, greenhouse gas emissions and plant growth. Resour. Conserv. Recycl. 161, 104924. doi: 10.1016/j.resconrec.2020.104924

CrossRef Full Text | Google Scholar

Supraja, K. V., Behera, B., Balasubramanian, P. (2020). Efficacy of microalgal extracts as biostimulants through seed treatment and foliar spray for tomato cultivation. Ind. Crop Prod. 151, 112453. doi: 10.1016/j.indcrop.2020.112453

CrossRef Full Text | Google Scholar

Tawaraya, K., Honda, S., Cheng, W., Chuba, M., Okazaki, Y., Saito, K., et al. (2018). Ancient rice cultivar extensively replaces phospholipids with non-phosphorus glycolipid under phosphorus deficiency. Physiol. Plantarum 163 (3), 297–305. doi: 10.1111/ppl.12699

CrossRef Full Text | Google Scholar

Toyokawa, C., Yamano, T., Fukuzawa, H. (2020). Pyrenoid starch sheath is required for LCIB localization and the CO2-concentrating mechanism in green algae. Plant Physiol. 182 (4), 1883–1893. doi: 10.1104/pp.19.01587

PubMed Abstract | CrossRef Full Text | Google Scholar

Umezawa, T. (2018). Lignin modification in planta for valorization. Phytochem. Rev. 17 (6), 1305–1327. doi: 10.1007/s11101-017-9545-x

CrossRef Full Text | Google Scholar

Vadiveloo, A., Foster, L., Kwambai, C., Bahri, P. A., Moheimani, N. R. (2021). Microalgae cultivation for the treatment of anaerobically digested municipal centrate (ADMC) and anaerobically digested abattoir effluent (ADAE). Sci. Total Environ. 775 (3), 145853. doi: 10.1016/j.scitotenv.2021.145853

PubMed Abstract | CrossRef Full Text | Google Scholar

Van Dijk, K. C., Lesschen, J. P., Oenema, O. (2016). Phosphorus flows and balances of the European union member states. Sci. Total Environ. 542, 1078–1093. doi: 10.1016/j.scitotenv.2015.08.048

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, J., Lei, Z., Tian, C., Liu, S., Wang, Q., Shimizu, K., et al. (2021). Ionic response of algal-bacterial granular sludge system during biological phosphorus removal from wastewater. Chemosphere 264, 128534. doi: 10.1016/j.chemosphere.2020.128534

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, Y., Spalding, M. H. (2014). Acclimation to very low CO2: Contribution of limiting CO2 inducible proteins, LCIB and LCIA, to inorganic carbon uptake in Chlamydomonas reinhardtii. Plant Physiol. 166 (4), 2040–2050. doi: 10.1104/pp.114.248294

PubMed Abstract | CrossRef Full Text | Google Scholar

Wuang, S. C., Khin, M. C., Chua, P. Q. D., Luo, Y. D. (2016). Use of spirulina biomass produced from treatment of aquaculture wastewater as agricultural fertilizers. Algal. Res. 15, 59–64. doi: 10.1016/j.algal.2016.02.009

CrossRef Full Text | Google Scholar

Wu, K., Wang, S., Song, W., Zhang, J., Wang, Y., Liu, Q., et al. (2020). Enhanced sustainable green revolution yield via nitrogen-responsive chromatic modulation in rice. Science 367 (6478), eaaz2046. doi: 10.1126/science.aaz2046

PubMed Abstract | CrossRef Full Text | Google Scholar

Wykoff, D. D., Grossman, A. R., Weeks, D. P., Usuda, H., Shimogawara, K. (1999). Psr1, a nuclear localized protein that regulates phosphorus metabolism in chlamydomonas. Proc. Natl. Acad. Sci. U.S.A. 96 (26), 15336–15341. doi: 10.1073/pnas.96.26.153

PubMed Abstract | CrossRef Full Text | Google Scholar

Yaakob, M. A., Mohamed, R. M. S. R., Al-Gheethi, A., Gokare, R. A., Ambati, R. R. (2021). Influence of nitrogen and phosphorus on microalgal growth, biomass, lipid, and fatty acid production: An overview. Cells 10 (2), 393. doi: 10.3390/cells10020393

PubMed Abstract | CrossRef Full Text | Google Scholar

Yadav, G., Dash, S. K., Sen, R. (2019). A biorefinery for valorization of industrial waste-water and flue gas by microalgae for waste mitigation, carbon-dioxide sequestration and algal biomass production. Sci. Total Environ. 688, 129–135. doi: 10.1016/j.scitotenv.2019.06.024

PubMed Abstract | CrossRef Full Text | Google Scholar

Yamano, T., Sato, E., Iguchi, H., Fukuda, Y., Fukuzawa, H. (2015). Characterization of cooperative bicarbonate uptake into chloroplast storoma in the green alga Chlamydomonas reinhardtii. Proc. Natl. Acad. Sci. U.S.A. 112 (23), 7315–7320. doi: 10.1073/pnas.1501659112

PubMed Abstract | CrossRef Full Text | Google Scholar

Yamano, T., Toyokawa, C., Shimamura, D., Matsuoka, T., Fukuzawa, H. (2022). CO2-dependent migration and relocation of LCIB, a pyrenoid-peripheral protein in Chlamydomonas reinhardtii. Plant Physiol. 188 (2), 1081–1094. doi: 10.1093/plphys/kiab528

PubMed Abstract | CrossRef Full Text | Google Scholar

Yamano, T., Tsujikawa, T., Hatano, K., Ozawa, S., Takahashi, Y., Fukuzawa, H. (2010). Light and low-CO2-dependent LCIB-LCIC complex localization in the chloroplast supports the carbon-concentrating mechanism in Chlamydomonas reinhardtii. Plant Cell Physiol. 51 (9), 1453–1468. doi: 10.1093/pcp/pcq105

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: microalga, sustainable agriculture, nutrient recycling, fertilizer alternative, CO2-concentrating mechanism, membrane lipid remodeling

Citation: Çakirsoy I, Miyamoto T and Ohtake N (2022) Physiology of microalgae and their application to sustainable agriculture: A mini-review. Front. Plant Sci. 13:1005991. doi: 10.3389/fpls.2022.1005991

Received: 28 July 2022; Accepted: 24 October 2022;
Published: 17 November 2022.

Edited by:

Qingfang He, University of Arkansas at Little Rock, United States

Reviewed by:

Alexei E. Solovchenko, Lomonosov Moscow State University, Russia
Sanjeev Mishra, Sardar Swaran Singh National Institute of Renewable Energy, India

Copyright © 2022 Çakirsoy, Miyamoto and Ohtake. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Takuji Miyamoto, tmiyamoto@sake.nu.niigata-u.ac.jp; Norikuni Ohtake, ohtake@agr.niigata-u.ac.jp

These authors have contributed equally to this work

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.