Literature DB >> 16347548

Production of vesicular-arbuscular mycorrhizal fungus inoculum in aeroponic culture.

L L Hung1, D M Sylvia.   

Abstract

Bahia grass (Paspalum notatum) and industrial sweet potato (Ipomoea batatas) colonized by Glomus deserticola, G. etunicatum, and G. intraradices were grown in aeroponic cultures. After 12 to 14 weeks, all roots were colonized by the inoculated vesicular-arbuscular mycorrhizal fungi. Abundant vesicles and arbuscules formed in the roots, and profuse sporulation was detected intra-and extraradically. Within each fungal species, industrial sweet potato contained significantly more roots and spores per plant than bahia grass did, although the percent root colonization was similar for both hosts. Mean percent root colonization and sporulation per centimeter of colonized root generally increased with time, although with some treatments colonization declined by week 14. Spore production ranged from 4 spores per cm of colonized root for G. etunicatum to 51 spores per cm for G. intraradices. Infectivity trials with root inocula resulted in a mean of 38, 45, and 28% of bahia grass roots colonized by G. deserticola, G. etunicatum, and G. intraradices, respectively. The germination rate of G. etunicatum spores produced in soil was significantly higher than that produced in aeroponic cultures (64% versus 46%) after a 2-week incubation at 28 degrees C. However, infectivity studies comparing G. etunicatum spores from soil and aeroponic culture indicated no biological differences between the spore sources. Aeroponically produced G. deserticola and G. etunicatum inocula retained their infectivity after cold storage (4 degrees C) in either sterile water or moist vermiculite for at least 4 and 9 months, respectively.

Entities:  

Year:  1988        PMID: 16347548      PMCID: PMC202456          DOI: 10.1128/aem.54.2.353-357.1988

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  2 in total

1.  Method for growing plants aeroponically.

Authors:  R W Zobel; P Del Tredici; J G Torrey
Journal:  Plant Physiol       Date:  1976-03       Impact factor: 8.340

2.  Maintaining cultures of ectomycorrhizal and plant pathogenic fungi in sterile water cold storage.

Authors:  D H Marx; W J Daniel
Journal:  Can J Microbiol       Date:  1976-03       Impact factor: 2.419

  2 in total
  6 in total

Review 1.  Methods for large-scale production of AM fungi: past, present, and future.

Authors:  Marleen Ijdo; Sylvie Cranenbrouck; Stéphane Declerck
Journal:  Mycorrhiza       Date:  2010-08-28       Impact factor: 3.387

2.  Extraction of extraradical arbuscular mycorrhizal mycelium from compartments filled with soil and glass beads.

Authors:  Elke Neumann; Eckhard George
Journal:  Mycorrhiza       Date:  2005-04-07       Impact factor: 3.387

3.  Sheared-root inocula of vesicular-arbuscular mycorrhizal fungi.

Authors:  D M Sylvia; A G Jarstfer
Journal:  Appl Environ Microbiol       Date:  1992-01       Impact factor: 4.792

4.  Fatty Acid methyl ester profiles for characterization of glomalean fungi and their endomycorrhizae.

Authors:  J H Graham; N C Hodge; J B Morton
Journal:  Appl Environ Microbiol       Date:  1995-01       Impact factor: 4.792

Review 5.  Technologies for beneficial microorganisms inocula used as biofertilizers.

Authors:  E Malusá; L Sas-Paszt; J Ciesielska
Journal:  ScientificWorldJournal       Date:  2012-04-01

Review 6.  Arbuscular mycorrhizal fungi and production of secondary metabolites in medicinal plants.

Authors:  YanYan Zhao; Annalisa Cartabia; Ismahen Lalaymia; Stéphane Declerck
Journal:  Mycorrhiza       Date:  2022-05-13       Impact factor: 3.856

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.