mycelial growth
traitmech:000074 · CLASS · REVIEWED
A morphology trait in which a bacterium grows as branching, filamentous hyphae that form a mycelium, often with subsequent differentiation into aerial hyphae and spores, as in Streptomyces.
Branching hyphal growth produces a bacterial mycelium
Edge evidence
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apical hyphal extension and branching
confers
mycelial growth
METPO:2007700Sustained apical extension and branching realize mycelial growth.
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DOI:10.1038/nrmicro1968
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mycelial growth
develops into
aerial hyphae and spore differentiation
biolink:develops_intoMycelial colonies differentiate aerial hyphae and spores.
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DOI:10.1038/nrmicro3178
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DivIVA polarisome
directs
apical hyphal extension and branching
RO:0002211The DivIVA polarisome drives apical (tip) growth of vegetative and aerial hyphae.
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DOI:10.1128/JB.00153-23
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polarisome splitting
causes
new branch emergence
biolink:causesSplitting of polarisomes at growing tips gives rise to daughter polarisomes that nucleate new branches.
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DOI:10.1093/femsml/uqad020
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CglA glycopolymer ligase
mediates
wall teichoic acid attachment to peptidoglycan
CglA catalyzes attachment of wall teichoic acids/glycopolymers to peptidoglycan during wall biogenesis.
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DOI:10.1128/mbio.01492-24
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CglA glycopolymer ligase
localizes to
hyphal tips and branching points
biolink:located_inCglA localizes to regions of active cell-wall incorporation at hyphal tips and branching points.
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DOI:10.1128/mbio.01492-24
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CglA glycopolymer ligase
enables
FtsZ-ring positioning and septum placement
RO:0002327Loss of CglA/glycopolymers disrupts FtsZ-ring formation/positioning and causes misplaced septa.
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DOI:10.1128/mbio.01492-24
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FtsZ Z-ladder arrays
drives
sporulation septation and spore-chain formation
Ladder-like arrays of FtsZ rings constrict and separate to yield regular spore chains.
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DOI:10.1128/mbio.01492-24
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SapB / chaplins / rodlins
promotes
aerial hyphae and spore differentiation
RO:0002213SapB surfactant and chaplin/rodlin sheaths overcome surface tension to promote aerial hyphae emergence.
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DOI:10.1093/femsml/uqad020
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Provenance
- Source
- METPO (2025-11-25)
- Definition source
- DOI:10.1038/nrmicro1968
Parent traits (1)
Synonyms (2)
- mycelium-forming
- hyphal growth
kg-microbe context
Matched 1 kg-microbe node via parent_proxy.
METPO:1000059[-2.682, -2.070, -3.656, -0.652, …]
Nearest neighbors in embedding space
- morphology polyhydroxyalkanoate granule 1.000
- environment cadmium tolerant 1.000
- environment cobalt tolerant 1.000
- environment copper tolerant 1.000
- environment desiccation tolerant 1.000
- environment piezotolerant 1.000
- morphology gas vesicle 1.000
- environment UV radiation tolerant 1.000
Deep research
# Curation report: bacterial mycelial growth ## Executive summary **Target:** `traitmech:000074` (quote verbatim) **Label:** mycelial growth **Category:** MORPHOLOGY **Parent:** `METPO:1000059` **Recommended graph scope:** the capacity of a bacterium—principally a filamentous actinomycete such as *Streptomyces*—to produce a **branched vegetative mycelium by polarized hyphal-tip extension and establishment of new lateral growth zones**. Vegetative hyphae are branched, hydrophilic, and generally multinucleoid; aerial hyphae are reproductive, comparatively unbranched and hydrophobic, and later septate into spores. Thus, aerial-hypha formation and sporulation are downstream developmental phenotypes, not necessary components of the core trait. (schlimpert2023thebestof pages 8-10, bhowmick2023osmoticstressresponses pages 1-2) The most defensible core mechanism is: > DivIVA-containing apical polarisome → spatial recruitment of cell-wall synthesis/remodeling machinery → polarized peptidoglycan insertion → hyphal-tip extension; budding or establishment of additional polarity centers → lateral branch formation → branched vegetative mycelium. Recent work adds CglA-dependent cell-wall glycopolymer attachment as a determinant of normal hyphal width and branching morphology. By contrast, SepIVA localizes with DivIVA but is dispensable under the tested conditions and should not be represented as required for mycelial growth. c-di-GMP primarily controls whether *Streptomyces* remains in vegetative mycelial growth or enters aerial development; it is better modeled as a developmental-state regulator than as a direct generator of branches. (sen2024adispensablesepiva pages 1-2, gallagher2024howcdigmpcontrols pages 1-3, bhowmick2024cellshapeand pages 1-2) ## 1. Trait scope and boundaries ### Included phenotype The trait comprises: 1. germ-tube or hyphal establishment; 2. persistent cell-wall growth at hyphal apices; 3. lateral establishment of new growth zones; 4. repeated extension and branching to form a connected vegetative filament network. A 2024 account states that vegetative *Streptomyces* hyphae “extend by polar cell wall growth and create new growth zones by lateral branching,” while clusters of DivIVA at tips form polarisomes involved in both apical growth and de novo branch establishment. (sen2024adispensablesepiva pages 1-2) ### Excluded or separately modeled boundary cases | Nearby phenotype | Relationship to `traitmech:000074` | Curation decision | |---|---|---| | Aerial-mycelium formation | Reproductive transition from vegetative growth; aerial hyphae differ in surface properties and branching pattern | Model as a downstream/alternative developmental state, not as part of the defining trait | | Sporulation and spore-chain formation | Septation and differentiation of aerial hyphae | Exclude from the core graph; connect through developmental-transition edges if useful | | Exploratory growth | Rapid surface expansion can involve long, relatively nonbranching vegetative hyphae after glucose depletion | Separate phenotype; it does not necessarily satisfy the branched-mycelium definition (schlimpert2023thebestof pages 8-10) | | Linear chains of divided cells | Filamentous appearance without apical hyphal growth and lateral branching | Exclude | | Wall-less S-cells | Vesicles extruded from tips under hyperosmotic or cell-wall stress | Stress-induced alternative morphology, not mycelial growth (schlimpert2023thebestof pages 8-10) | | Pellets, clumps, dispersed mycelia | Macroscopic submerged-culture architectures formed by aggregation and branching | Treat as assay/bioprocess phenotypes downstream of mycelial growth, not synonyms | | Fungal mycelium | Morphologically analogous but taxonomically and mechanistically distinct | Exclude from this bacterial trait graph | | Filamentous cyanobacteria | Usually chains of communicating cells produced by division rather than *Streptomyces*-type polar hyphal extension | Exclude unless the trait definition is deliberately broadened | ## 2. Candidate nodes ### Trait and taxa - `traitmech:000074` — mycelial growth. - `METPO:1000059` — supplied parent trait. - *Streptomyces* spp.; key experimental systems: *S. coelicolor* and *S. venezuelae*. - *Streptomyces variegatus* — taxon used in the ROS/pyrogallol branching work. - *Lentzea aerocolonigenes* — application-relevant filamentous actinomycete. Taxon CURIEs should be added only after checking the current NCBI Taxonomy records for the precise strain; strain-level identifiers are not inferred here. ### Proteins and complexes - **DivIVA** — essential polarity determinant; central polarisome scaffold. - **Scy** — coiled-coil polarisome-associated scaffold affecting polarisome organization/branching. - **FilP** — intermediate-filament-like protein providing mechanical organization to growing hyphae. - **AfsK** — Ser/Thr protein kinase that phosphorylates DivIVA during cell-wall stress.
Curation history
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PROPOSED_FROM_RESEARCH · claude
Proposed candidate MORPHOLOGY trait (mycelial growth) from literature research to fill the multicellular/developmental gap.
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CURATED_CAUSAL_GRAPH · claude
Added evidence-backed causal graph (branching hyphal growth / differentiation) with RO/biolink predicate groundings; promoted PROPOSED to REVIEWED.
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ENRICH_CAUSAL_GRAPH · claude
Added 7 evidence-backed generic edges (10 new nodes) from the deep-research report.
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GROUND_CAUSAL_PREDICATES · claude
Grounded 5 causal-edge predicate_id field(s) via mappings/predicate_grounding.tsv (RO:0002211×1, biolink:causes×1, biolink:located_in×1, RO:0002327×1, RO:0002213×1).
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MIGRATE_ENABLES_TRAIT_EDGES · claude
Migrated 1 causal edge(s) off enables/RO:0002327 with a TRAIT object (1 to confers), issue 302. RO:0002327 has range 'biological process or activity', which a trait (a disposition) cannot satisfy, so the previous form entailed trait is-a BiologicalProcessOrActivity. The replacements are proposed in proposals/metpo_traitmech_v8 and are placeholder ids until METPO mints them.