Fact-checked by Grok 2 weeks ago

Nostoc

Nostoc is a of filamentous in the family Nostocaceae and order Nostocales, characterized by prokaryotic cells that form macroscopic, gelatinous colonies composed of intertwined trichomes—chains of vegetative cells interspersed with specialized heterocysts for and akinetes for . These colonies typically appear as spherical or irregularly shaped masses, ranging from microscopic to over 20 in diameter, embedded in a mucilaginous of extracellular that provides protection and structural integrity. The trichomes are unbranched and often coiled, with cells containing chlorophyll a and phycobiliproteins that impart a blue-green hue, though colonies can darken to brown or black due to environmental factors or pigments. Reproduction occurs primarily through fragmentation of trichomes or formation of hormogonia (short motile filaments), enabling rapid dispersal and colonization. Nostoc species thrive in diverse habitats, including nutrient-poor freshwater bodies like ponds and lakes, as well as semi-terrestrial environments such as moist , rocks, and biological soil crusts in arid or regions. They exhibit remarkable tolerance to environmental stresses, including , freezing, high UV , and limitation, with growth rates as slow as doubling times of 2–3 years in some species like Nostoc zetterstedtii. Notable species include , which forms sheet-like colonies in terrestrial settings and produces antimicrobial compounds, and Nostoc flagelliforme, a drought-resistant form harvested as in some cultures. Ecologically, Nostoc plays a crucial role in , contributing to and in oligotrophic ecosystems, and it forms symbiotic associations with like and fungi in lichens. In agricultural contexts, such as rice paddies, it enhances soil levels, while in natural settings, it aids in crust formation and . Some species can produce or antibiotics, influencing microbial communities; certain are harmful to humans and animals.

Biology

Morphology and Cellular Structure

Nostoc species form macroscopic colonies that are typically gelatinous, bead-like, or spherical masses, ranging from microscopic to several centimeters in diameter, often appearing green or brown due to pigmentation. These colonies, such as those of Nostoc pruniforme, can reach up to 25 cm across, while N. commune commonly produces spheres or discoid crusts up to 3 cm in diameter or extensive mats. The cohesive structure arises from a mucilaginous sheath that envelops the filaments, providing protection and enabling the colony to maintain integrity in diverse environments. At the microscopic level, Nostoc consists of unbranched filaments known as , composed primarily of cylindrical vegetative cells measuring approximately 4-8 μm in length and 3-5 μm in width. These filaments are interspersed with specialized cells: heterocysts, which are colorless, thicker-walled structures about 5-7 μm in diameter specialized for , and akinetes, which are enlarged resting spores with thick walls, typically 8-12 μm long, adapted for and dispersal. The vegetative cells are barrel-shaped or spherical, dividing crosswise to elongate the , while heterocysts and akinetes occur at intervals along the trichome, with akinetes often positioned midway between heterocysts. The surrounding the trichomes is a key feature, consisting of an extracellular that facilitates and offers physical against and environmental stress. This varies in thickness and pigmentation among ; for instance, in N. commune, it forms a prominent, yellowish-brown, laminar envelope that expands into lamellae up to 10 cm wide, composed of heteropolysaccharides rich in glucose, , and other monosaccharides. In N. punctiforme, the contributes to irregular, amorphous , enhancing embedding within the gelatinous .

Reproduction and Life Cycle

Nostoc, a of filamentous , reproduces exclusively asexually, with no evidence of observed across ; genetic arises primarily through during vegetative growth. The primary mode of reproduction is fragmentation of trichomes, where filaments break into smaller segments that regrow into new colonies under favorable conditions. These fragments often develop into hormogonia, short motile filaments lacking heterocysts that glide via secretion to disperse and establish new colonies, typically lasting 1-2 days before differentiating into vegetative filaments. Hormogonia formation is triggered by environmental cues such as nitrogen limitation or host signals in symbiotic contexts, facilitating colony expansion. A key survival strategy in the Nostoc life cycle involves akinetes, thick-walled dormant cells formed from vegetative cells under stress conditions like nutrient scarcity, high light intensity, or desiccation; these akinetes accumulate storage compounds and can remain viable for years. Germination of akinetes occurs when conditions improve, such as increased moisture, moderate temperatures (around 20-27°C), and light exposure (e.g., 100 μmol m⁻² s⁻¹), leading to the emergence of new trichomes that resume vegetative growth. For instance, akinetes of Nostoc commune have enabled revival of desiccated colonies after over 100 years of dormancy, demonstrating exceptional resilience to extreme aridity and cold. The of Nostoc encompasses three main stages: vegetative , where filaments expand and perform and ; akinete dormancy for enduring adverse environments; and hormogonia-mediated dispersal for . Heterocysts, specialized cells for , form periodically along trichomes in response to low oxygen or levels, supporting during the vegetative phase but are absent in hormogonia to prioritize . Environmental triggers like light quality, nutrient availability, and stress thus regulate transitions between stages, ensuring to fluctuating habitats.

Physiology and Metabolism

Nostoc species perform oxygenic primarily in their vegetative cells, utilizing as the primary pigment alongside accessory phycobilins such as and , which enhance light harvesting in the 500–650 nm range. This process generates oxygen and organic compounds, but to enable simultaneous , Nostoc maintains spatial separation between oxygen-producing vegetative cells and anoxic heterocysts, preventing inactivation of the oxygen-sensitive enzyme. In heterocysts, photosynthetic activity is reduced, with largely absent to minimize , while supports cyclic electron transport for ATP generation. Nitrogen fixation in Nostoc occurs exclusively within , where the enzyme complex converts atmospheric dinitrogen (N₂) to (NH₃) via the reaction N₂ + 8H⁺ + 8e⁻ → 2NH₃ + H₂, requiring substantial energy input of approximately 16 ATP molecules per N₂ fixed. The heterocyst envelope, composed of laminated layers and a matrix, acts as a barrier to oxygen, while respiratory processes consume any residual oxygen to maintain an microenvironment. This adaptation allows diazotrophic growth under nitrogen-limiting conditions, with fixed exported as or glutamate to support vegetative . Carbon fixation in Nostoc proceeds via the Calvin-Benson cycle in vegetative cells, where ribulose-1,5-bisphosphate carboxylase/oxygenase () incorporates CO₂ into 3-phosphoglycerate, ultimately yielding carbohydrates. Fixed carbon is stored as , a β-1,4-linked glucose , for energy reserves during periods of darkness or stress, or as cyanophycin, a non-ribosomally synthesized polyamino acid serving as a and carbon depot. These storage mechanisms enable metabolic flexibility, particularly in nutrient-variable environments. Key physiological adaptations in Nostoc include the creation of conditions in heterocysts through thick cell walls that restrict gas and enhanced respiration to scavenge oxygen, ensuring functionality. For tolerance, species such as Nostoc punctiforme accumulate , a that stabilizes proteins and membranes during dehydration by maintaining cellular hydration and preventing phase transitions in lipids. This osmoregulatory response allows revival upon rehydration without loss of viability. Nostoc produces secondary metabolites like scytonemin, a lipid-soluble that absorbs UV radiation (λ_max 370 nm and 384 nm) to protect against DNA damage and in exposed habitats. Some strains also synthesize microcystins, cyclic hepatotoxic peptides that may deter grazers or provide allelopathic advantages, though production varies by environmental cues and . Recent genomic studies, such as the 2022 whole-genome sequencing of Nostoc sp. CCCryo 231-06 using microfluidic single-cell , have revealed genes encoding adaptations, including those for enhanced osmotic response, UV repair, and cold-active enzymes, underscoring Nostoc's metabolic versatility in harsh conditions. Subsequent research as of 2025 includes proteomic analyses of N. commune highlighting geotypic variations in responses (2024) and demonstrations of Nostoc sp. PCC7120's capability for P450-mediated of pesticides like , expanding insights into metabolic applications.

Ecology

Habitat and Distribution

Nostoc species are widely distributed across diverse terrestrial and aquatic environments, exhibiting a cosmopolitan range from tropical to polar regions. In terrestrial habitats, they commonly colonize nutrient-poor soils, rocks, and moist surfaces, particularly in temperate and polar areas. For instance, N. commune forms gelatinous colonies on bare soils and rock outcrops in semi-arid and arid regions, contributing to biological soil crusts that stabilize surfaces in places like the and polar deserts. These thrive in fluctuating wet-dry cycles, tolerating prolonged while remaining metabolically inactive until rehydration triggers recovery. Aquatic habitats for Nostoc primarily include freshwater systems such as oligotrophic to mesotrophic ponds, lakes, and paddies, where they form benthic or planktonic colonies in nutrient-limited conditions. Species like N. pruniforme are prevalent in temperate and sub-Arctic lakes with low (0.7 mM or higher) and levels (<0.3 µM), while N. sphaeroides occurs in paddy fields across southern and central China, aiding in nitrogen fixation during wet seasons. Although rare in marine environments, some strains, such as N. sphaeroides from brackish coastal lagoons like Chilika Lake in India, demonstrate limited tolerance to saline-alkaline conditions. Nostoc is abundant in nitrogen-limited ecosystems globally, from the Arctic tundra to tropical wetlands, but shows sensitivity to pollution that disrupts low-nutrient preferences. Extreme environments highlight Nostoc's resilience, with cryophilic strains enduring freezing temperatures down to -60°C in Arctic and Antarctic tundras and polar lakes, and desiccation-tolerant forms surviving in hyper-arid s of the Gobi Desert and Sonoran Desert. These adaptations allow persistence in habitats with extreme temperature swings (0–35°C optimal, but tolerating -40°C to 78°C) and pH ranges of 3–10, though aquatic species prefer neutral to alkaline conditions (pH >7). Climate influences, such as warming-induced shifts in moisture regimes, may alter distribution patterns in vulnerable polar and arid zones, as observed in recent monitoring of crust dynamics. Overall, Nostoc's low requirements and broad environmental underpin its global prevalence in resource-poor ecosystems.

Symbiotic and Ecological Interactions

Nostoc species form mutualistic symbioses with various , providing fixed in exchange for carbohydrates. In the , Trichormus azollae (formerly known as Nostoc azollae), a closely related cyanobacterium in the family Nostocaceae, resides in leaf cavities and fixes atmospheric via heterocysts, supporting the 's in nutrient-poor waters and serving as a natural in paddies. Genomic analyses of culturable Nostoc strains from reveal multiple gene clusters, including Mo- and V-nitrogenases, enhancing fixation efficiency and enabling infection of additional hosts like the liverwort Blasia. Nostoc also acts as the cyanobiont (phycobiont) in lichens such as Peltigera species, supplying photosynthates and nitrogen to the fungal partner while receiving protection and nutrients. In these associations, symbiotic Nostoc expresses fasciclin domain proteins that promote cell adhesion, facilitating stable integration within the lichen thallus. Similarly, Nostoc forms symbioses with bryophytes, including hornworts (Phaeoceros and Leiosporoceros) and liverworts (Blasia), where it fixes nitrogen using both molybdenum- and vanadium-nitrogenase systems encoded on plasmids, potentially acquired via horizontal transfer. As primary producers, Nostoc colonizes pioneer communities in barren soils and aquatic environments, initiating succession through oxygenic photosynthesis and nitrogen fixation. Its gelatinous sheaths bind soil particles, stabilizing surfaces and preventing erosion in arid or disturbed terrestrial habitats. In oligotrophic lakes, Nostoc cycles nitrogen by fixing dinitrogen and releasing ammonium, supporting microbial and algal communities in low-nutrient conditions. Nostoc engages in competitive interactions with other for light and resources, often dominating mats through rapid growth and production. It faces predation by grazers such as protozoans and , though its thick sheaths and microcystin-like s confer resistance. Allelopathic compounds from Nostoc inhibit competing , potentially liberating to fuel blooms in nutrient-cycling dynamics. Research has shown Nostoc-like cyanobacterial strains in coral reefs, such as those associated with species, aiding nutrient cycling through in oligotrophic marine settings. Polyphasic studies of new Nostoc isolates reveal diverse metabolic adaptations, including enhanced carbon uptake influenced by heterotrophic bacteria, underscoring interdependence in symbiotic microbiomes. These findings emphasize Nostoc's role as a bacterial hub in plant symbioses. Nostoc mats profoundly impact microbial communities by altering diversity through spatial structuring and metabolite exchange, fostering specialized consortia. Their oxygen production via photosynthesis creates oxic microzones, influencing adjacent anaerobic processes and redox gradients in benthic ecosystems.

Applications

Culinary and Historical Uses

Nostoc species, particularly Nostoc flagelliforme and Nostoc commune, have been utilized in traditional cuisines across Asia for over 2,000 years, often as a delicacy or survival food during famines. In China, N. flagelliforme, known as "facai" or "hair vegetable," has been harvested from arid steppes and incorporated into soups and stir-fries since ancient times, symbolizing prosperity during Chinese New Year celebrations due to its phonetic resemblance to "get rich" in Cantonese. Similarly, N. commune, referred to as "ishikurage" in Japan, has been consumed as a food ingredient and folk remedy, valued for its gelatinous texture in vinegared dishes or stews. In the Peruvian highlands, N. commune serves as a seasonal dietary staple, eaten raw or in local stews called picante, highlighting its role in indigenous diets in high-altitude regions. Culinary preparation typically involves wild harvesting from moist soils or fields, followed by sun-drying to form , thread-like strands that rehydrate easily for cooking. These dried forms are soaked to restore their slippery, noodle-like consistency before being added to hot pots, salads, or vegetarian dishes like . Nostoc sphaeroides, for instance, is collected from paddies and prepared as "Ge-Xian-Mi" or "hairy " in soups, mimicking the texture of seaweeds in Japanese-inspired recipes. Edible contain no known toxins, with confirmed through long-term human consumption and toxicity studies showing no adverse effects. However, foragers must distinguish them from potentially toxic look-alikes, such as certain Anabaena , by their macroscopic, gelatinous colonies and lack of foul odor. Nutritionally, edible Nostoc provides high protein levels, typically 25-27% of dry weight, along with essential , vitamins (including B12 analogs), and minerals like iron and calcium, making it a valuable in nutrient-scarce diets. These attributes have sustained its use as a in historical contexts, such as in arid regions, and contribute to its emerging role in vegan as a protein-rich, gluten-free alternative in blends and plant-based meals. Despite these benefits, intensive wild harvesting, especially of N. flagelliforme, has led to concerns, including in due to overcollection and habitat disruption. Efforts to cultivate like N. sphaeroides aim to mitigate these issues while preserving cultural traditions.

Biotechnological Applications

Nostoc species produce a variety of bioactive compounds with potential industrial applications, particularly and peptides derived from their extracellular polymeric substances and . extracted from exhibit moisturizing properties suitable for cosmetic formulations, owing to their high molecular weight and anionic , which support hydration and . These compounds also demonstrate anti-allergic effects by inhibiting release from mast cells, making them promising for skincare products. Additionally, nostocyclopeptides, cyclic nonribosomal heptapeptides unique to Nostoc, possess activity against and fungi, positioning them as candidates for novel antibiotics. Their antitoxic properties further extend to counteracting uptake in hepatocytes, enhancing their pharmaceutical relevance. In pharmaceutical development, Nostoc-derived metabolites show promise for therapeutic interventions. Cryptophycins, potent depsipeptide antimitotic agents isolated from Nostoc sp. strain GSV 224, exhibit strong anti-cancer activity against multidrug-resistant tumor cell lines, including ovarian and breast carcinomas, by disrupting dynamics at picomolar to nanomolar concentrations. Exopolysaccharides () from Nostoc sp. strains such as PCC 7936 and PCC 7413 promote through biocompatibility and enhanced migration and proliferation , forming hydrogels that accelerate tissue repair. These , composed of multiple monosaccharides with groups, yield over 1,300 mg/L under optimized culture conditions, supporting scalable production for dermal applications. Genetic engineering of Nostoc leverages recent genomic advancements for applications. Whole-genome sequencing of strains like Nostoc sp. CCCryo 231-06 in 2022 has revealed pathways, enabling targeted / edits to enhance N-fixing efficiency in Nostoc punctiforme. These tools, including RNA-guided transposition systems, facilitate production by optimizing metabolic pathways for and accumulation, with ongoing developments through 2025 improving efficiency in filamentous strains. In agriculture, Nostoc serves as an effective biofertilizer inoculant, particularly for rice cultivation. Application at 10 kg/ha fixes 20-30 kg N/ha in flooded fields, boosting crop yields by 10-30% through improved nitrogen availability and growth promotion via indole-3-acetic acid and vitamins. This reduces chemical fertilizer needs by up to 25-50%, enhancing sustainability in paddy systems. Recent studies highlight Nostoc's potential in clean energy, with heterocyst-forming strains engineered for enhanced hydrogen production. In Nostoc PCC 7120, heterologous expression of clostridial [FeFe]-hydrogenases in heterocysts yields sustained photobiological H₂ output under nitrogen limitation, with 2022-2025 research optimizing electron flux for rates up to several micromoles per mg chlorophyll per hour. These advances address oxygen sensitivity, positioning Nostoc as a viable platform for renewable biofuel generation.

Environmental and Remediation Uses

Nostoc species demonstrate significant potential in soil through of , leveraging their extracellular and structures to bind contaminants such as (Cd) and lead (). For instance, Nostoc muscorum exhibits removal efficiencies ranging from 12.5% for to 81.8% for lead in contaminated soils, primarily via adsorption on cell surfaces. Similarly, achieves up to 90% removal of and 10% for after 45 days in treated mine tailings, highlighting its applicability in stabilizing polluted sites like abandoned areas. Nostoc linckia further supports remediation of copper-contaminated soils by tolerating and accumulating metals through mechanisms. These processes not only reduce metal but also enhance in degraded environments. In applications, Nostoc forms robust that facilitate the and uptake of pollutants, including in eutrophic systems. Axenic of Nostoc muscorum effectively sequester from , with scalable removal from effluents, demonstrating up to high efficiency in . For management, Nostoc ellipsosporum removes up to 36.42% of from textile via cellular uptake and , aiding in the mitigation of in -rich lakes. Passively Nostoc species in reactors further treat municipal by promoting adsorption and , offering a phototrophic alternative to conventional methods. Nostoc contributes to adaptation by sequestering carbon in gelatinous mats and providing inputs to degraded lands. Terrestrial mats of contribute to annual net carbon fixation rates of up to 21 g C m⁻² year⁻¹ in extreme environments like dry valleys, driven by temperature and regimes. In post-fire landscapes, Nostoc inoculation in biological soil crusts (biocrusts) promotes , increasing soil organic by 30-100% in degraded African soils and aiding recovery of nutrient-poor sites. These mats also support revegetation in fire-affected areas by stabilizing soil and supplying fixed , as seen in biocrust efforts that improve in arid, post-disturbance ecosystems. Case studies illustrate Nostoc's practical deployment in environmental restoration. In rice paddies, systems enhance Nostoc populations, boosting biological and contributing up to significant portions of crop needs without synthetic fertilizers, as observed in mountainous fields where Ge-Xian-Mi (Nostoc sphaeroides) naturally colonizes for winter fertilization. Recent research from 2023-2025 on recovery highlights Nostoc's role in biocrusts, where it colonizes post-thaw soils to fix and sequester carbon, supporting microbial in warming polar regions and aiding ecosystem resilience against climate-induced degradation. Despite these benefits, limitations include the potential for release during uncontrolled blooms, necessitating careful . Certain Nostoc s, such as Nostoc sp. 152, produce nostophycin, a cyclic depsipeptide toxic to and fungi and potentially harmful if blooms occur in remediation sites. Additionally, excessive proliferation in nutrient-enriched waters can lead to hypoxic conditions, underscoring the need for controlled and environmental oversight to prevent adverse ecological impacts.

Taxonomy and Phylogeny

Classification History

The genus Nostoc was first formally recognized in by in his (1753), where he described species such as under the name "Nostoch," derived from the alchemical term "nostoch" coined by in the 16th century to describe gelatinous terrestrial substances resembling fallen stars or nostril mucus. This early naming reflected a rudimentary understanding of the organism as a peculiar alga-like entity. In 1803, Jean-Pierre-Étienne Vaucher established Nostoc as a distinct within the in his Histoire des conferves aquatiques, emphasizing its filamentous, gelatinous colonial form and separating it from other algal groups based on macroscopic and microscopic observations. During the 19th and early 20th centuries, Nostoc was classified within the Myxophyceae (), a group treated as primitive due to their photosynthetic capabilities and lack of apparent cellular , though their prokaryotic nature was not yet appreciated. Comprehensive monographs by Édouard Bornet and Charles Flahault (1886–1888) in Révision des Nostocacées hétérocystées provided the foundational framework, describing over 200 species based primarily on traits such as filament arrangement, presence, and formation, while revising earlier classifications and establishing Nostoc as the of the Nostocaceae family. This era solidified Nostoc's position in phycological , with species delineations relying heavily on habitat-specific and colonial variability. A pivotal shift occurred in 1971 when Ralph Y. Stanier and colleagues recognized blue-green algae, including Nostoc, as prokaryotes in their seminal review, reclassifying them under based on cellular , DNA composition, and phylogenetic relatedness to rather than eukaryotes. This led to the adoption of the term "" and prompted ongoing taxonomic revisions. Post-2000, polyphasic approaches integrating morphological, ecological, and molecular data—such as 16S rRNA gene sequencing and secondary structure analysis of the 16S-23S rRNA —have refined classifications, revealing Nostoc as polyphyletic and necessitating genus-level splits. Recent revisions from 2022 to 2025 have further fragmented the traditional Nostoc complex: for instance, the genus Aliinostoc was erected in 2018 but expanded in subsequent studies to accommodate morphologically similar but genetically distinct lineages previously lumped in Nostoc, with new species described through polyphasic methods. Similarly, Amazonocrinis was established in 2021 for epilithic and symbiotic strains from diverse habitats, with species like A. thailandica (2022) and A. malviyae (2023) highlighting phylogenetic inconsistencies via phylogenomic analyses. Within the core Nostoc genus, new species such as N. montejanii were described in 2023 from Mexican high-elevation wetlands, based on combined morphological and genetic evidence. These updates underscore ongoing taxonomic challenges, including cryptic species diversity driven by high phenotypic plasticity, where environmental factors induce variable filament morphology, akinete production, and colony forms, complicating delineation without molecular tools.

Current Species and Diversity

Nostoc belongs to the family Nostocaceae within the order Nostocales and the phylum , encompassing filamentous cyanobacteria capable of through specialized cells. The of the is Nostoc commune, which serves as the benchmark for taxonomic descriptions within the group. Following recent taxonomic revisions based on molecular data, approximately 50 are currently accepted in the genus Nostoc, though this number reflects ongoing lumping and splitting due to polyphasic approaches integrating morphology, ecology, and genetics. Prominent species include N. commune, a cosmopolitan form known for its terrestrial and aquatic colonies that are edible in various cultures; N. punctiforme, widely studied as a model for symbiotic interactions with and fungi; and N. flagelliforme, valued commercially for its hair-like thalli used in traditional and . Phylogenetic analyses of Nostoc primarily rely on 16S rRNA gene sequencing for genus-level placement, supplemented by multi-locus sequence typing using genes such as rbcL, psbA, and rpoC1 to resolve boundaries and intraspecific variation. A 2025 study in Frontiers in Microbiology classified 38 Nostoc-like strains isolated from paddy soils, reassigning many to related genera like Aliinostoc, Aulosira, and Desmonostoc based on concatenated 16S rRNA and rbcL phylogenies, highlighting the genus's paraphyletic nature in traditional classifications. The diversity within Nostoc is shaped by morphological convergence, where similar gelatinous colony forms across strains often lead to taxonomic revisions, as seen in the discordance between phenotypic traits and molecular phylogenies. Ecological niches, including terrestrial, , and symbiotic habitats, drive by selecting for adaptations in motility, frequency, and stress tolerance, resulting in clade-specific distributions. Recent taxonomic additions underscore this dynamic diversity; for instance, N. tlalocii, described in 2023 as a endemic from high-altitude wetlands, was delineated using 16S rRNA sequences (98.5% similarity to closest relatives) alongside distinct and vegetative cell morphologies.

Human Impacts

Conservation and Threats

Nostoc populations, particularly those forming biological soil crusts in arid and semi-arid regions, face significant loss from agricultural expansion and , which disrupt mats through , application, and infrastructure development. For instance, in China's paddy fields, agricultural changes including use have reduced natural stands of Nostoc sphaeroides by destroying gelatinous colonies essential for . Similarly, river development associated with threatens Nostoc verrucosum in cool, clear streams of , where limits recolonization of disturbed areas. These activities degrade the thin layers where terrestrial Nostoc thrives, leading to and loss of nitrogen-fixing capabilities in ecosystems like deserts and steppes. Pollution from agricultural fertilizers exacerbates these pressures by promoting in aquatic and semi-aquatic habitats. Herbicides from runoff further inhibit Nostoc sphaeroides growth in fields, contributing to localized population declines. poses additional risks by altering wet-dry cycles critical for desiccation-tolerant Nostoc species, potentially disrupting their revival after periods in arid environments. Increased temperatures and erratic in deserts are projected to reduce cover, including Nostoc-dominated communities, impairing and soil fertility. Recent analyses (2022-2023) highlight how could exacerbate these effects in . Overharvesting has severely impacted Nostoc flagelliforme in , where commercial collection for culinary use since the has caused scarcity and ecological degradation in arid steppes. Intensive harvesting damaged vast grasslands in , , , and , converting approximately 1.6 hectares of land per 450g collected into through and loss of crusts, while accelerating sandstorms. In response, 's State Council banned collection and trade in 2000, but prior led to population crashes and increased counterfeiting due to high market value. Few Nostoc species have been formally assessed by the IUCN, reflecting underrepresentation of in global red lists, though N. flagelliforme is classified as nationally endangered in and listed as a level-one key protected wild plant due to and threats. hotspots such as the and remain at high risk, where combined pressures could lead to further losses of endemic strains integral to . A 2025 review emphasizes the ongoing need for enhanced monitoring of Nostoc populations in arid regions amid . Effective monitoring of Nostoc populations requires genomic tracking to assess and track declines, as demonstrated by phylogenomic analyses of 151 strains revealing overlooked variation in arid-adapted lineages vulnerable to fragmentation.

Management Strategies

Conservation efforts for Nostoc emphasize both habitat protection and ex situ preservation to safeguard endemic populations, particularly in arid and semi-arid regions where like Nostoc flagelliforme are vulnerable to . Protected areas in , such as steppe reserves, help maintain natural habitats for these , preventing further degradation from grazing and climate impacts. Ex situ strategies include laboratory culturing and strain preservation in collections like the Indonesian Indigenous Cyanobacteria Culture Collection, which stores diverse Nostoc isolates for conservation and research. For instance, techniques ensure long-term viability of strains, such as those in the Culture Collection of Cryophilic , supporting recovery efforts for threatened morphotypes. Cultivation of Nostoc has advanced through controlled systems to meet demands for and agricultural uses, reducing pressure on wild populations. In , biofertilizer production farms utilize Nostoc strains like N. piscinale in rice paddies, where inoculation enhances . methods, including thin-layer raceway ponds, enable scalable growth of species such as N. calcicola under optimized light and nutrient conditions, yielding suitable for and remediation applications. Regulation of Nostoc harvesting focuses on sustainable practices, especially for commercially valuable species in . For N. flagelliforme, authorities impose harvest quotas and licensing to curb overexploitation in and provinces, where annual collections once exceeded sustainable levels due to high market demand. Pollution controls, such as nutrient runoff restrictions in agricultural watersheds, mitigate risks that could disrupt Nostoc-dominated biocrusts, aligning with broader environmental policies to preserve cyanobacterial ecosystems. Restoration techniques leverage Nostoc's nitrogen-fixing capabilities to rehabilitate degraded lands. inoculation with strains like N. commune has proven effective in increasing organic carbon, aggregation, and microbial diversity in desertified steppes, with improvements in cover observed in field trials. Integration into systems involves applying Nostoc inoculants alongside cover crops to enhance in sustainable farming, promoting long-term resilience without synthetic inputs. Ongoing research highlights the need for polyphasic monitoring approaches, combining morphological, genetic, and physiological analyses, to assess invasive risks from introduced or biotech-modified Nostoc strains, particularly in 2025 projections amid climate-driven range expansions. Policy development for biotech strains emphasizes risk assessment frameworks to prevent unintended ecological disruptions, building on studies of cyanobacterial bloom dynamics. International frameworks under the Convention on Biological Diversity (CBD) guide microbial conservation, including protocols for accessing and benefiting from Nostoc genetic resources via the Nagoya Protocol, which ensures equitable sharing of biotechnological innovations derived from these cyanobacteria.

References

  1. [1]
  2. [2]
    Ecophysiology of gelatinous Nostoc colonies - PubMed Central - NIH
    The cyanobacterial genus Nostoc includes several species forming centimetre-large gelatinous colonies in nutrient-poor freshwaters and harsh semi-terrestrial ...
  3. [3]
    Phycokey - Nostoc - UNH Center for Freshwater Biology
    In PhycoKey you can find Nostoc either as a colony or a filament because it is a colony of filaments. Morphology: Spherical colonies of twisted trichomes ...
  4. [4]
    Nostoc - an overview | ScienceDirect Topics
    Cells of Nostoc spp. are spherical, barrel-shaped, or oval forming unbranched filaments. The filaments (trichomes) may contain both heterocysts (thick walled, ...
  5. [5]
    Nostoc - an overview | ScienceDirect Topics
    Cells are cylindrical to barrel shaped, sometimes elongated in the central part of the trichome; apical cells are rounded. Heterocytes are solitary and ...
  6. [6]
    Nostoc: the smallest multicellular organism – Inanimate Life
    Nostoc is a genus of cyanobacteria that is common in a variety of habitats: soil, ponds and growing on the surface of rocks and soil if they are kept moist.
  7. [7]
    Classification of Nostoc-like cyanobacteria isolated from ... - Frontiers
    May 19, 2025 · This study aims to classify 38 new isolated Nostoc–like strains at the genus level. The relationship between phylogenetic classification and morphological ...
  8. [8]
    Structural characteristic of polysaccharide isolated from Nostoc ...
    Dec 22, 2022 · Nostoc commune is a species of lower heterocystous blue-green alga capable of forming an extended jelly layer consisted of polysaccharides, ...<|control11|><|separator|>
  9. [9]
    Reproduction and Dispersal of Biological Soil Crust Organisms
    They can reproduce sexually, or asexually by fragmentation of filaments or simple cell division, by autospores (non-motile cells formed inside the mother cell ...<|control11|><|separator|>
  10. [10]
  11. [11]
    Characteristics of Hormogonia Formation by Symbiotic Nostoc spp ...
    Nostocacean cyanobacteria typically produce gliding filaments termed hormogonia at a low frequency as part of their life cycle.Missing: reproduction asexual akinetes
  12. [12]
    Survival and Development Strategies of Cyanobacteria through ...
    Mar 4, 2024 · This review covers the cyanobacterial akinete of the Nostocales order and summarizes the environmental triggers and cellular responses involved in akinete ...
  13. [13]
    Environmental factors affecting akinete germination and resting cell ...
    Jan 17, 2023 · Our study reveals the optimum conditions for the germination and growth of cyanobacterial akinetes and resting cells isolated from river sediment, respectively.Missing: paper | Show results with:paper
  14. [14]
    Full article: Dried Nostoc commune exhibits nitrogen-fixing activity ...
    Apr 6, 2022 · The filamentous cells in dried colonies survive for more than 100 years without differentiation into akinetes/spores.
  15. [15]
    The regulation of photosynthetic pigments in terrestrial Nostoc ...
    The phycobilins are unique among the photosynthetic pigments in that they are bonded to certain proteins, known as phycobiliproteins, which are commonly divided ...
  16. [16]
    Cyanobacterial Heterocysts - PMC - NIH
    Heterocysts are terminally differentiated cells that are specialized morphologically and physiologically for supplying fixed nitrogen to the filament.
  17. [17]
    Formation and maintenance of nitrogen-fixing cell patterns ... - PNAS
    May 9, 2016 · N2 fixation is catalyzed by nitrogenase, and this enzyme is easily degraded by oxygen. Some filamentous cyanobacteria have developed a mechanism ...
  18. [18]
    nitrogen stress-inducible small RNA regulates CO2 fixation in Nostoc
    The small RNA nitrogen stress-inducible RNA 4 (NsiR4) regulates two enzymes involved in CO2 fixation in cyanobacteria.
  19. [19]
    Central metabolism and development are rewired in lichenized ...
    In Nostoc, nitrogen fixation occurs in specialized cells called heterocysts, which create a microoxic environment required for the activity of nitrogenase ...
  20. [20]
    Cyanophycin and glycogen synthesis in a cyanobacterial ...
    Presumably photosynthetic carbon reduction via the Calvin cycle was also not inhibited by 150 mM NaCl, because the cells also accumulated the carbon/energy ...
  21. [21]
    Review article Cyanophycin and arginine metabolism in cyanobacteria
    Cyanophycin serves as a transient storage of nitrogen that is very relevant in the fixation of atmospheric nitrogen. Cyanophycin is synthesized non-ribosomally ...<|separator|>
  22. [22]
    Water-stress induced trehalose accumulation and control of ...
    Aug 6, 2025 · Some Nostoc species are known to be tolerant to desiccation and to accumulate trehalose [58] .
  23. [23]
    Metabolites Facilitating Adaptation of Desert Cyanobacteria to ... - NIH
    Nov 24, 2022 · In this review, we discuss the metabolic pathways used by desert cyanobacteria to adapt to extreme arid conditions.
  24. [24]
    Scytonemin: Unravelling major progress and prospects
    Scytonemin is one such secondary metabolite, exploited mainly for its photoprotective function and found exclusively in many cyanobacterial species from ...Missing: microcystins | Show results with:microcystins
  25. [25]
    The First Proteomic Study of Nostoc sp. PCC 7120 Exposed ... - MDPI
    PCC 7120 is known as a model nitrogen-fixing organism with a complete genome sequence and well-developed genetic techniques [15]. It is important to underline ...
  26. [26]
    Whole genome sequencing of cyanobacterium Nostoc sp. CCCryo ...
    May 20, 2022 · This work uses a microfluidic platform for Nostoc single cell sequencing. This technology provides minimal contamination in single cell sequencing.
  27. [27]
    Nostoc Flagelliforme - an overview | ScienceDirect Topics
    The terrestrial cyanobacterium Nostoc flagelliforme was harvested in the Gobi Desert and the Qinghai Plateau and traditionally consumed in China and Mongolia ...
  28. [28]
    Distribution and ecology of the edible cyanobacterium Ge-Xian-Mi ...
    Aug 9, 2025 · 4). Nostoc sphaeroides is widely distributed in the mountainous paddy fields of Southern or Central China while historically it was thriving in ...Missing: polar brackish
  29. [29]
    Biogenic synthesis of silver-nanoparticles with the brackish water ...
    The aim of this study was to isolate a filamentous nitrogen-fixing cyanobacterium Nostoc sphaeroides (NS) from brackish water of Chilika Lake, Odisha coast.
  30. [30]
    Comparative genomic insights into culturable symbiotic ... - NIH
    Abstract. Species of the floating, freshwater fern Azolla form a well-characterized symbiotic association with the non-culturable cyanobacterium Nostoc ...
  31. [31]
    Fasciclin Domain Proteins Are Present in Nostoc Symbionts of Lichens
    The type of structures where the symbiont is housed include root (cycad), leaf (Azolla), stem (Gunnera), and thallus (bryophyte and lichen). There are different ...
  32. [32]
    Complete Genomes of Symbiotic Cyanobacteria Clarify the ... - NIH
    We present four complete genomes of cyanobacteria isolated from bryophytes. Nanopore long-read sequencing allowed us to obtain circular contigs for all the ...Cyanobiont Genome Assemblies · A Conserved Vnf Cluster In... · Literature Cited<|separator|>
  33. [33]
    The ecology of Nostoc | Request PDF - ResearchGate
    Aug 7, 2025 · Nostoc is somewhat resistant to predation; this probably is related to production of large amounts of sheath material, synthesis of ...
  34. [34]
    New insights into the habitat shifts of odor-producing terrestrial ...
    Terrestrial cyanobacteria, especially Nostoc, metabolize organic carbon better than cyanobacteria from other habitats. Organic matter applied to the culture ...
  35. [35]
    The Nostoc-Gunnera symbiosis - PubMed
    This review gives an updated account of present knowledge concerning the Nostoc-Gunnera symbiosis. Emphasis will be on the development of the symbiotic ...
  36. [36]
    Nitrogen liberated via allelopathy can promote harmful algal blooms
    Allelopathy is a biological mechanism that can promote harmful algal blooms (HAB) via the inhibition of sympatric phytoplankton.
  37. [37]
    Symbioses of Cyanobacteria in Marine Environments: Ecological ...
    Cyanobacteria are capable to embrace symbiotic relationships in marine environments with organisms such as protozoans, macroalgae, seagrasses, and sponges.
  38. [38]
    Competition and interdependence define interactions of Nostoc sp ...
    Mar 8, 2025 · Our study indicates a limited autonomy of symbiotic Nostoc strains, which may also explain its preference for symbiotic interactions.
  39. [39]
    Metabarcoding reveals unique microbial mat communities and ...
    Mar 24, 2024 · High‐sulfur, low‐oxygen environments formed by underwater sinkholes and springs create unique habitats populated by microbial mat communities.
  40. [40]
    Impacts of microbial assemblage and environmental conditions on ...
    Feb 26, 2019 · All microbial communities were dominated by one or two cyanobacterial species, so the key mat metabolisms involve oxygenic photosynthesis and ...
  41. [41]
    Edible Terrestrial Cyanobacteria for Food Security in the Context of ...
    Nostoc flagelliforme has been consumed in China for more than 2000 years, valued as a delicacy known as “Facai” (hair-like vegetable) [18]. Its bioactive ...
  42. [42]
    [PDF] Chinese studies on the edible blue-green alga, Nostoc flagelliforme
    Nostoc flagelliforme experiences extreme environ- mental changes in nature. The habitats of N. flagelli- forme are located 1000–2800 m above sea level, and are ...
  43. [43]
    Fat choy: the lucky sounding Chinese New Year food whose ...
    Jan 28, 2024 · Fat choy, or black moss, is a Chinese New Year food with a lucky name meaning 'get rich' in Cantonese, but overharvesting has caused desert.
  44. [44]
    Cyanobacteria (Nostoc commune) used as a dietary item in the ...
    Jun 19, 2008 · Throughout highland Peru, Nostoc commune is highly salient as a seasonal dietary item, being eaten alone, or in picante – a local stew – and is ...Missing: Native | Show results with:Native
  45. [45]
    Microalgae: From staple foodstuff to avant-garde cuisine
    Grown in arid regions of western China the cyanobacterium Nostoc flagelliforme--called fa cai in Mandarin and fat choy in Cantonese--is wild-harvested and ...
  46. [46]
    Purification and Characterization of Corrinoid-Compounds ... - J-Stage
    Vitamin B12 content (98.8±5.6 μg/100 g dry weight) of an edible cyanobacterium, Nostoc commune (Ishikurage) was determined by the Lactobacillus delbrueckii ...
  47. [47]
    In vitro and in vivo safety assessment of edible blue-green algae ...
    This study was undertaken to evaluate in vitro and in vivo toxicity of cultivated Nostoc commune var. sphaeroides Kützing (NO) and Spirulina platensis (SP).Missing: alikes | Show results with:alikes
  48. [48]
    Nostoc Num Nums - Eat The Weeds and other things, too
    is an essential ingredient ...Missing: Norse bread
  49. [49]
    Healthy efficacy of Nostoc commune Vaucher - PMC - NIH
    In spite of a long history of usage in the medicinal cuisine of oriental regions and countries, until approximately 20 years ago, only a limited number of ...Missing: star bread
  50. [50]
    Physicochemical Evaluation of Cushuro (Nostoc sphaericum ...
    May 10, 2023 · Nostoc cyanobacteria, whose protein content is 25.4 g, 1076 mg of calcium, and 19.6 mg of iron per 100 g of Nostoc on a dry basis, constitutes ...
  51. [51]
    (PDF) Edible Terrestrial Cyanobacteria for Food Security in the ...
    May 16, 2025 · Nostoc sphaeroides a valuable resource for food and bioactive compounds [26,27,59]. Nostoc sphaericum can be cultivated under controlled ...<|control11|><|separator|>
  52. [52]
    An in vitro study shows the potential of Nostoc commune ...
    An in vitro study shows the potential of Nostoc commune (Cyanobacteria) polysaccharides extract for wound-healing and anti-allergic use in the cosmetics ...Missing: antibiotics nostocyclopeptides
  53. [53]
  54. [54]
    Total Structures of Cryptophycins, Potent Antitumor Depsipeptides ...
    Total Structures of Cryptophycins, Potent Antitumor Depsipeptides from the Blue-Green Alga Nostoc sp. Strain GSV 224 | Journal of the American Chemical Society.
  55. [55]
    Biochemical characterization of Nostoc sp. exopolysaccharides and ...
    In this study, the EPS produced by the Nostoc sp. strains PCC7936 and PCC7413 were characterized and evaluated as a biomaterial for new wound dressings.Missing: anti- cancer calothrixins
  56. [56]
    (PDF) Whole Genome Sequencing of Cyanobacterium Nostoc sp ...
    Genome sequencing of single microbial cells in low biomass settings such as in extreme conditions could lead to crucial findings in astrobiological pursuits.
  57. [57]
    Customized molecular tools to strengthen metabolic engineering of ...
    Recently, genome engineering using RNA-guided transposition with a CRISPR-associated transposase was reported for Nostoc 7120 and Golden Gate vectors [80].
  58. [58]
    Microbes as Biofertilizers, a Potential Approach for Sustainable Crop ...
    They fix 20–30 Kg/N/ha in submerged rice fields and increase crop yield by 10–15% when applied at 10 Kg/ha. Reportedly, N availability to plants was increased ...
  59. [59]
    Advances and challenges in photosynthetic hydrogen production
    Avilan, et al. Phototrophic hydrogen production from a clostridial [FeFe] hydrogenase expressed in the heterocysts of the cyanobacterium Nostoc PCC 7120.Review · Cyanobacterial And Algal... · In Vivo Hydrogen Production...
  60. [60]
  61. [61]
    Macroscopic cyanobacteria of the genus Nostoc
    Nostoc commune (Linnaeus) Vaucher ex Bornet et. Flahault. (Linnaeus, 1753: 1157; Vaucher, 1803: 203; Bornet &. Flahault, 1888: 203–207). Type collection. Old ...<|control11|><|separator|>
  62. [62]
    [PDF] Taxonomic classification of cyanoprokaryotes (cyanobacterial ...
    The whole classification of cyanobacteria (species, genera, families, orders) has undergone exten- sive restructuring and revision in recent years with the ...
  63. [63]
    Nostoc Vaucher ex Bornet & Flahault, 1886 - AlgaeBase
    From several described subgenera are probably acceptable typical Nostoc and Amorphonostoc, which differ in morphology of colonies (Amorphonostoc has no ...Missing: Linnaeus | Show results with:Linnaeus
  64. [64]
    Purification & properties of unicellular blue-green algae
    1 June 1971. Share on. Purification and properties of unicellular blue-green algae (order Chroococcales). Authors: R Y Stanier, R Kunisawa, M Mandel, G Cohen ...Missing: prokaryotes | Show results with:prokaryotes
  65. [65]
    Taxonomy of cyanobacteria: a contribution to consensus approach
    Jul 24, 2014 · This article reviews the present status of the taxonomy of cyanobacteria, describes earlier, classical and recent taxonomic approaches and the trends for ...
  66. [66]
    [PDF] Description of two new species of Nostoc from China based ... - Fottea
    Two new Nostoc species, Nostoc favosum and Nostoc mirabile, were described using a polyphasic approach, with unique 16S-23S rRNA ITS secondary structure.Missing: post- | Show results with:post-
  67. [67]
    Description of two new species of Aliinostoc and ... - Oxford Academic
    Nov 15, 2018 · This paper describes two new species of the cyanobacterial genus Aliinostoc and a new species of Desmonostoc.
  68. [68]
    Amazonocrinis nigriterrae gen. nov., sp. nov., Atlanticothrix silvestris ...
    The cyanobacterial genus Nostoc is an important contributor to carbon and nitrogen bioavailability in terrestrial ecosystems and a frequent partner in symbiotic ...
  69. [69]
    Amazonocrinis thailandica sp. nov. (Nostocales, Cyanobacteria), a ...
    Mar 15, 2022 · Two novel Amazonocrinis strains isolated from a rice field in the central region of Thailand were characterized using a polyphasic approach.Missing: paddies brackish
  70. [70]
    Description of two new species of Nostoc (Nostocales ...
    Oct 27, 2023 · This phenotypic plasticity, seen both in the field and in cultured samples, continues to make taxonomy difficult, and many Nostoc-like ...
  71. [71]
    Phylogenetically distant clade of Nostoc-like taxa with the ...
    Nostoc is a complex and tough genus to differentiate, and its morphological plasticity makes it taxonomically complicated. Its cryptic diversity and almost ...
  72. [72]
    Nostoc caeruleum var. planctonicum (Poretzky & Tschernov) B.A. ...
    The type species (lectotype) of the genus Nostoc is Nostoc commune Vaucher ex Bornet & Flahault. This name is of an entity that is currently accepted ...
  73. [73]
    Taxonomic History and State of Knowledge of the Marine Species in ...
    Jul 30, 2025 · Our updated list of Nostocales from the Mexican Atlantic presents 45 currently taxonomically valid species, distributed in 19 genera and eight ...
  74. [74]
    Molecular Mechanisms of Nostoc flagelliforme Environmental ...
    This review explores recent advancements in the molecular mechanisms that enable N. flagelliforme to survive under such harsh conditions.
  75. [75]
    Phylogenetic analysis of Nostocales (Cyanobacteria) based on two ...
    Structural nitrogenase genes (nifH, nifK and nifD) as well as 16S rRNA have been shown to be adequate genetic markers for distinguishing cyanobacterial genera.
  76. [76]
    How discordant morphological and molecular evolution among ...
    Aug 25, 2014 · More recent molecular analyses show discordance in estimates of biodiversity based on morphological analyses. Moreover, phylogenetic analyses of ...
  77. [77]
    Bioclimatic factors at an intrabiome scale are more limiting than ...
    Jul 12, 2018 · The presence of these two phylogroups in the northernmost localities results in a higher Nostoc diversity in the northern portion of the SN ...
  78. [78]
    Description of two new species of Nostoc (Nostocales ...
    Oct 27, 2023 · The present study describes two new Nostoc species, N. montejanii and N. tlalocii, based on a polyphasic approach that combines morphological, ecological, and ...
  79. [79]
    [PDF] Biological Soil Crusts: Ecology and Management - USDA ARS
    This publication covers Biological Soil Crusts: Ecology & Management, and was jointly funded by USDI, BLM, and USGS.Missing: urbanization | Show results with:urbanization
  80. [80]
    Will “Air Eutrophication” Increase the Risk of Ecological Threat to ...
    Jul 10, 2023 · We synthesize recent evidence showing the possibility that accelerating eutrophication will spill over from aquatic ecosystems to the atmosphere via “air ...
  81. [81]
    Biocrust nitrogenase activity responses to warming and increased ...
    Dec 15, 2022 · Changes in temperature and precipitation are expected to influence the function of desert ecosystems by altering the biogeochemical cycles ...
  82. [82]
    Impact of warming on Nostoc colonies (Cyanobacteria) in a wet ...
    The warming effects on primary productivity were investigated during summer seasons 2009 and 2010 in cyanobacterial colonies of Nostoc commune s.l., which plays ...
  83. [83]
    Cross-Site Comparisons of Dryland Ecosystem Response to Climate ...
    Aug 16, 2022 · This Overview article synthesizes over 40 years of research on ecosystem response to climate change at diverse dryland sites.
  84. [84]
    Discriminating authentic Nostoc flagelliforme from its counterfeits by ...
    Therefore, the State Council of China banned the collection and trade of N. flagelliforme in 2000. Currently, the scarcity of this Chinese delicacy and the ...
  85. [85]
    [PDF] Factors causing dune ephemeral wetlands to be vulnerable to weed ...
    The small stature of indigenous ephemeral wetland species predisposes them to be out-competed and displaced by taller and/or faster-growing alien species ( ...
  86. [86]
    A taxonomic inventory of national key protected wild plants in ...
    Jan 23, 2023 · Among them, Nosloc flagelliforme is a level-one key protected wild plant, and 52 species and one variety are level-two key protected Wild plants ...
  87. [87]
    Rapid Radiations Outweigh Reticulations During the Evolution ... - NIH
    Oct 1, 2025 · Here, we used 151 genomes and metagenome-assembled genomes (MAGs) to characterize genomic species boundaries in Nostoc within a phylogenomic ...
  88. [88]
    Population genomics and morphological data bridge the centuries of ...
    Apr 19, 2024 · We compiled a dataset of morphological data from 180 cultured strains and 300 whole genome sequences, including eight herbarium specimens and ...