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Ultrastructural aspects of the hyphal tip ofSclerotium rolfsii preserved by freeze substitution

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Summary

The hyphal tip ofSclerotium rolfsii was examined after fixation by freeze substitution. The Spitzenkörper consisted of a dense mass of apical vesicles and microvesicles surrounding a vesicle-free zone. Linear arrangements of microvesicles were occasionally observed within the Spitzenkörper. Abundant microfilaments were seen within the Spitzenkörper region, often in close association with apical vesicles and microvesicles. Microtubules passed through the Spitzenkörper and terminated at the plasmalemma at the extreme hyphal apex. Filasomes were mostly observed within the apical region and were in close proximity to the plasmalemma. Rough ER, mitochondria, microtubules, and vacuoles were abundant in the subapical region and were usually oriented parallel to the long axis of the hypha. Ribosomes were aligned on the outer surfaces of mitochondria. Golgi body equivalents were observed throughout the subapical region and appeared as inflated cisternae of varying shapes and electron opacities. Relationships to other basidiomycetous hyphal tip cells are discussed.

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Abbreviations

AV:

apical vesicle

C:

Celsius

diam:

diameter

f:

filasome

G:

Golgi body equivalent

h:

hour

nm:

nanometer

M:

mitochondria

ME:

membranous elements; min minute

MV:

microvesicle

MVB:

multivesicular body

N:

nucleus

OsO4 :

osmium tetroxide

R:

ribosome

ER:

endoplasmic reticulum

S:

Spitzenkörper

Va:

vacuole

μm:

micrometer

References

  • Bennett WF, Gutierrez-Hartmann A, Butow RA (1976) The role of mitochondria-bound 80 S ribosomes in mitochondrial biogenesis. In:Bucher TH, Neupert W, Sebald W, Werner S (eds) Genetics and biogenesis of chloroplasts and mitochondria. Elsevier/North-Holland Biomedical Press, Amsterdam, pp 801–806

    Google Scholar 

  • Bracker CE, Grove SN (1971) Continuity between cytoplasmic endomembranes and outer mitochondrial membranes in fungi. Protoplasma 73: 15–34

    PubMed  Google Scholar 

  • Franke WW, Kartenbeck J (1971) Outer mitochondrial membrane continuous with endoplasmic reticulum. Protoplasma 73: 35–41

    PubMed  Google Scholar 

  • Girbardt M (1969) Die Ultrastruktur der Apikalregion von Pilzhyphen. Protoplasma 67: 413–441

    Google Scholar 

  • Gooday SN (1983) The hyphal tip. In:Smith JE (ed) Fungal differentiation. A contemporary synthesis. Dekker, New York Basel, pp 315–356

    Google Scholar 

  • Grove SN, Bracker CE (1970) Protoplasmic organization of hyphal tips among fungi: vesicles and Spitzenkörper. J Bacteriol 104: 989–1009

    PubMed  Google Scholar 

  • —,Sweigard JA (1981) The Spitzenkörper core persists after tip growth is arrested by cytochalasins. Mycol Soc Am Newslett 32: 33

    Google Scholar 

  • Harold FM, Kropf DL, Caldwell JH (1985) Why do fungi drive electric currents through themselves? Exp Mycol 9: 183–186

    Google Scholar 

  • Herr FB, Heath MC (1982) The effects of antimicrotubular agents on organelle positioning in the cowpea rust fungus,Uromyces phaseoli var.vignae. Exp Mycol 6: 15–24

    Google Scholar 

  • Hoch HC (1986) Freeze-substitution of fungi. In:Aldrich HC, Todd WJ (eds) Ultrastructure techniques for microorganisms. Plenum, New York, pp 183–2121

    Google Scholar 

  • —,Howard RJ (1980) Ultrastructure of freeze-substituted hyphae of the basidiomyceteLaetisaria arvalis. Protoplasma 103: 281–297

    Google Scholar 

  • —,Staples RC (1983 a) Ultrastructural organization of the non-differentiated uredospore germling ofUromyces phaseoli. Mycologia 75: 795–824

    Google Scholar 

  • Howard RJ (1981) Ultrastructural analysis of hyphal tip cell growth in fungi: Spitzenkörper, cytoskeleton and endomembranes after freeze-substitution. J Cell Sci 48: 89–103

    PubMed  Google Scholar 

  • —,Aist JR (1979) Hyphal tip cell ultrastructure of the fungusFusarium: improved preservation by freeze-substitution. J Ultrastruct Res 66: 224–234

    PubMed  Google Scholar 

  • — — (1980) Cytoplasmic microtubules and fungal morphogenesis: Ultrastructural effects of methyl benzimidazole-2-ylcarbamate determined by freeze-substitution of hyphal tip cells. J Cell Bio 87: 55–64

    PubMed  Google Scholar 

  • —,O'Donnell KL (1987) Freeze substitution of fungi for cytological analysis. Exp Mycol 11: 249–269

    Google Scholar 

  • Jaffe LF, Robinson KR, Nuccitelli R (1974) Local cation entry and self-electrophoresis as an intracellular localization mechanism. Ann N Y Acad Sci 238: 372–389

    PubMed  Google Scholar 

  • Kellems RE, Butow RA (1972) Cytoplasmic-type 80 S ribosomes associated with yeast mitochondria. I. Evidence for ribosome binding sites on yeast mitochondria. J Biol Chem 247: 8043–8050

    PubMed  Google Scholar 

  • —,Allison VF, Butow RA (1974) Cytoplasmic type 80 S ribosomes associated with yeast mitochondria. II. Evidence for the association of cytoplasmic ribosomes with the outer mitochondria membranein situ. J Biol Chem 249: 3297–3303

    PubMed  Google Scholar 

  • Keyhani E (1973) Ribosomal granules associated with outer mitochondrial membrane in aerobic yeast cells. J Cell Bio 58: 480–484

    Google Scholar 

  • McClure WK, Park D, Robinson PM (1968) Apical organization in the somatic hyphae of fungi. J Gen Microbiol 50: 177–182

    PubMed  Google Scholar 

  • Mims CW, Roberson RW, Richardson EA (1988) Ultrastructure of freeze-subsituted and chemaiclly fixed basidiospores ofGymnosporangium juniperi-virginianae. Mycologia 80: 356–364

    Google Scholar 

  • Morre DL, Merritt WD, Lembi CA (1971) Connections between mitochondria and endoplasmic reticulum in rat liver and onion stem. Protoplasma 73: 43–49

    PubMed  Google Scholar 

  • Newhouse JR, Hoch HC, MacDonald WL (1983) The ultrastructure ofEndothia parasitica. Comparison of a virulent with a hypovirulent isolate. Can J Bot 61: 389–399

    Google Scholar 

  • Reynolds ES (1963) The use of lead citrate at high pH as an electronpaque stain in electron microscopy. J Cell Biol 17: 208–212

    PubMed  Google Scholar 

  • Rowley CR, Moran DT (1975) A simple procedure for mounting wrinkle-free sections on formvar-coated slot grids. Ultramicroscopy 1: 151–155

    PubMed  Google Scholar 

  • Wessels JGH (1986) Cell wall synthesis in apical hyphal growth. Int Rev Cytol 104: 37–79

    Google Scholar 

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Roberson, R.W., Fuller, M.S. Ultrastructural aspects of the hyphal tip ofSclerotium rolfsii preserved by freeze substitution. Protoplasma 146, 143–149 (1988). https://doi.org/10.1007/BF01405923

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