Review: Mekanisme Miko-Heterotrof Tumbuhan Monotropa

2020 ◽  
Vol 3 (2) ◽  
pp. 49
Author(s):  
Nuril Azizah ◽  
Gita Ayu Khoirunnisa ◽  
Nuril Nuzulia ◽  
Reza Selvyana Muhammad ◽  
Mukhamad Su'udi
Keyword(s):  

Monotropa merupakan Angiospermae yang tidak berkolofil sehingga tidak mampu untuk melakukan fotosintesis. Monotropa mendapatkan nutrisi untuk pertumbuhan dan perkembangannya melalui mekanisme miko-heterotrof, yaitu dengan berasosiasi dengan jamur mikoriza.  Mikoriza bersimbiosis dengan akar tumbuhan autotrof untuk mendapatkan hasil fotosintesis, nutrisi tersebut kemudian ditransfer ke tumbuhan Monotropa. Sel-sel hifa yang berhubungan dengan epidermis akar tumbuhan autotrof dan Monotropa merupakan titik transfer nutrisi. Hifa mikoriza akan membentuk selubung (sheath) ke akar tumbuhan yang kemudian akan membentuk struktur hartig net yang menembus epidermis akar. Hartig net akan terus mengintrusi ke sel korteks akar yang kemudian akan membentuk fungal pegs. Fungal pegs ini yang akan menginduksi terbentuknya transfer sel untuk mentransfer nutrisi dari mikoriza ke Monotropa

1990 ◽  
Vol 68 (3) ◽  
pp. 579-593 ◽  
Author(s):  
H. B. Massicotte ◽  
R. L. Peterson ◽  
C. A. Ackerley ◽  
L. H. Melville

The ontogeny and ultrastructure of ectomycorrhizae synthesized between Betula alleghaniensis (yellow birch) and Pisolithus tinctorius, a broad host range fungus, were studied to determine the structural modifications in both symbionts during ectomycorrhiza establishment. A number of stages, including initial contact of hyphae with the root surface, early mantle formation, and mature mantle formation, were distinguished. Interactions between hyphae and root hairs were frequent. As a paraepidermal Hartig net developed, root epidermal cells elongated in a radial direction, but wall ingrowths were not formed. Repeated branching of Hartig net hyphae resulted in extensive fine branches and the compartmentalization of hyphal cytoplasm. Nuclei and elongated mitochondria were frequently located in the narrow cytoplasmic compartments, and [Formula: see text] thickenings developed along walls of cortical cells in primary roots.


1989 ◽  
Vol 46 (Supplement) ◽  
pp. 737s-740s ◽  
Author(s):  
I. Kottke ◽  
F. Oberwinkler
Keyword(s):  

2000 ◽  
Vol 35 (9) ◽  
pp. 1905-1910 ◽  
Author(s):  
EDUARDO LUIZ VOIGT ◽  
VETÚRIA LOPES DE OLIVEIRA ◽  
ÁUREA MARIA RANDI

Compatibility between Eucalyptus dunnii and the ectomycorrhizal fungi Hysterangium gardneri and Pisolithus sp. - from Eucalyptus spp. -, Rhizopogon nigrescens and Suillus cothurnatus - from Pinus spp.-, was studied in vitro. Pisolithus sp., H. gardneri and S. cothurnatus colonized the roots. Pisolithus sp. mycorrhizas presented mantle and Hartig net, while H. gardneri and S. cothurnatus mycorrhizas presented only mantle. S. cothurnatus increased phenolics level on roots. Pisolithus sp. and R. nigrescens decreased the level of these substances. The isolates from Eucalyptus seem to be more compatible towards E. dunnii than those from Pinus. The mechanisms involved could be related, at least in the cases of Pisolithus and Suillus, to the concentration of phenolics in roots.


PERENNIAL ◽  
2010 ◽  
Vol 6 (1) ◽  
pp. 11
Author(s):  
Melya Riniarti ◽  
Irdika Mansur ◽  
Arum Sekar Wulandari ◽  
Cecep Kusmana

Morphology and anatomy characteristics often used to identify ectomycorrhizal fungi. We used three Scleroderma spp. (Scleroderma columnare, S. dictyosporum), and S. sinnamariense) and inoculated to Shorea pinanga, Pinus merkusii, and Gnetum gnemon. After 6,8, and 10 months, each root tips were collected to determined hyphae colour, branching pattern, clamp-connection, hartig net and mantle. This result revealed that S. sinnamariense did not form association with S. pinanga and P. merkusii but form association with G. gnemon. On the other hand, S. columnare and S. dictyosporum could form association with all the host plants. S. columnare and S. dictyosporum formed white hyphae while S. sinnamariense formed yellow hyphae with monopodial branching pattern. The depth of hartig net and mantle was increased by timed. Key words: ectomycorrhizal fungi, hartig net, mantle, Scleroderma


2019 ◽  
Vol 222 (4) ◽  
pp. 1951-1964 ◽  
Author(s):  
Gang Sa ◽  
Jun Yao ◽  
Chen Deng ◽  
Jian Liu ◽  
Yinan Zhang ◽  
...  

1989 ◽  
Vol 67 (6) ◽  
pp. 1717-1726 ◽  
Author(s):  
Ken K. Y. Wong ◽  
Yves Piché ◽  
Diane Montpetit ◽  
Bradley R. Kropp

First-order laterals of Pinus banksiana seedlings were inoculated with variant strains of ectomycorrhizal Laccaria bicolor in an aseptic culture system. Macroscopic observations of 10 fungal strains indicated that 6 are mycorrhizal and 4 are apparently nonmycorrhizal. Furthermore, light microscopic examinations revealed significant intraspecific variation in mycorrhizal structures. The mean mantle thickness, mean mantle density, and mean Hartig net penetration of the six mycorrhizal strains ranged from 2.5 to 13.4 hyphae, 278 to 411 hyphae/mm and 2 to 2.8 root cell layers, respectively. Three of these strains formed fewer macroscopically observable mycorrhizae and developed significantly thinner mantles but their Hartig nets usually separated cortical cells more extensively. Three of the four apparently nonmycorrhizal strains showed infrequent and poor Hartig net development (mean penetration of 0.3 to 0.8 root cell layer), poor surface colonization, and no mantle development. These three strains were better able to colonize long roots. Only one strain could be considered truly nonmycorrhizal because it only colonized root surfaces poorly and never showed mantle or Hartig net formation. The observed intraspecific variability raises questions concerning the determinants of mycorrhiza development and structure.


1986 ◽  
Vol 64 (1) ◽  
pp. 177-192 ◽  
Author(s):  
H. B. Massicotte ◽  
R. L. Peterson ◽  
C. A. Ackerley ◽  
Y. Piché

Alnus crispa (Ait.) Pursh seedlings were grown in plastic pouches and inoculated with Frankia to induce nodules and subsequently with Alpova diplophloeus (Zeller & Dodge) Trappe & Smith to form ectomycorrhizae. The earliest events in ectomycorrhiza formation involved contact of the root surface by hyphae, hyphal proliferation to form a thin mantle, and further hyphal growth to form a thick mantle. Structural changes in the host, the mycosymbiont, and the fungus–epidermis interface were described at various stages in the ontogeny of ectomycorrhizae. Fungal hyphae in contact with epidermal cells in the regions of intercellular penetration and paraepidermal Hartig net developed numerous rough endoplastic reticulum cisternae. In more proximal regions of the mycorrhiza, these gradually became fewer in number and smooth. A complicated labyrinthine wall branching system also developed in the fungus in these regions. Concurrently, epidermal cells formed wall ingrowths in regions adjacent to Hartig net hyphae. There was a gradient in the formation of these epidermal transfer cells as the mycorrhiza developed, and an additional deposition of secondary cell wall over the wall ingrowths occurred as transfer cells senesced. Nonmycorrhizal control roots did not develop epidermal wall ingrowths. Electron-dense material, which was also autofluorescent, was deposited in the outer tangential walls of the exodermis contiguous to the paraepidermal Hartig net.


1989 ◽  
Vol 67 (1) ◽  
pp. 201-210 ◽  
Author(s):  
H. B. Massicotte ◽  
C. A. Ackerley ◽  
R. L. Peterson

Ultrastructural features of the two symbionts in ectomycorrhizae formed between Alnus rubra and Alpova diplophloeus change with developmental stage. In the root cap – meristem zone, hyphae penetrate between vacuolated root cap cells and become appressed to epidermal cells containing small vacuoles, plastids with starch, numerous Golgi bodies, mitochondria, and endoplasmic reticulum cisternae. In the young Hartig net zone, hyphae with few vacuoles penetrate between vacuolated epidermal cells that still contain numerous Golgi bodies but now have plastids with small starch grains. Hartig net hyphae begin to branch and eventually form a complex branching system in the mature Hartig net zone. Hartig net hyphae in the basal portion of the ectomycorrhizae synthesize lipid and finally become vacuolated.


1987 ◽  
Vol 17 (8) ◽  
pp. 846-854 ◽  
Author(s):  
H. B. Massicotte ◽  
C. A. Ackerley ◽  
R. L. Peterson

Seedlings of Alnuscrispa (Ait.) Pursh, Alnusrubra Bong., Eucalyptuspilularis Sm., and Betulaalleghaniensis Britt. were grown in plastic pouches and subsequently inoculated with Alpovadiplophloeus (Zeller & Dodge) Trappe & Smith (two different strains), Pisolithustinctorius (Pers.) Coker & Couch, and Laccariabicolor (R. Mre) Orton, respectively, to form ectomycorrhizae insitu. Alnus seedlings were inoculated with Frankia prior to inoculation with the mycosymbiont. The interface established between A. crispa and A. diplophloeus was complex, involving wall ingrowth formation in root epidermal cells and infoldings in Hartig net hyphae. Alnusrubra – A. diplophloeus ectomycorrhizae had an interface lacking epidermal cell wall ingrowths but with infoldings in Hartig net hyphae. The interface between E. pilularis –. tinctorius consisted of branching Hartig net hyphae between radially enlarged epidermal cells lacking wall ingrowths. Ectomycorrhizae between B. alleghaniensis and L. bicolor developed unique interfaces with radially enlarged epidermal cells near the apical meristem, which synthesized dense vacuolar deposits. Very fine branchings occurred in Hartig net hyphae.


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