Literature DB >> 3120792

Carbon and nitrogen metabolism in ectomycorrhizal fungi and ectomycorrhizas.

F Martin1, M Ramstedt, K Söderhäll.   

Abstract

The literature concerning the metabolism of carbon and nitrogen compounds in ectomycorrhizal associations of trees is reviewed. The absorption and translocation of mineral ions by the mycelia require an energy source and a reductant which are both supplied by respiratory catabolism of carbohydrates produced by the host plant. Photosynthates are also required to generate the carbon skeletons for amino acid and carbohydrate syntheses during the growth of the mycelia. Competition for photosynthates occurs between the fungal cells and the various vegetative sinks in the host tree. The nature of carbon compounds involved in these processes, their routes of metabolism, the mechanisms of control and the partitioning of metabolites between the various sites of utilization are only poorly understood. Both ascomycetous and basidiomycetous ectomycorrhizal fungi synthesize and some, if not all, accumulate mannitol, trehalose and triglycerides. The fungal strains employ the Embden--Meyerhof pathway of glucose catabolism and the key enzymes of the pentose phosphate pathway (6-phosphogluconate dehydrogenase, glucose-6-phosphate dehydrogenase, transaldolase and transketolase). Anaplerotic CO2 fixation, via pyruvate carboxylase and/or phosphoenolpyruvate carboxykinase, provides high pools of amino acids. This process could be important in the recapture and assimilation of respired CO2 in the rhizosphere. The ectomycorrhizas are thought to contain the Embden--Meyerhof pathway, the pentose phosphate pathway and the tricarboxylic acid cycle, which provide the carbon skeletons for the assimilation of ammonia into amino acids. The main route of assimilation of ammonia appears to be through the glutamine synthetase-glutamate synthase cycle in the ectomycorrhizas. Glutamate dehydrogenase plays a minor role in this process. Glutamate dehydrogenase and glutamine synthetase are present in free-living ectomycorrhizal fungi and they participate in the assimilation of ammonia and the synthesis of amino acids through the glutamate dehydrogenase/glutamine synthetase sequence. In both in vitro cultures of fungi and ectomycorrhizas, the assimilated nitrogen accumulates in glutamine. Glutamine, but also ammonia, are thought to be exported from the fungal tissues to the host cells. Studies on the metabolism of ectomycorrhizas and ectomycorrhizal fungi have focused on the metabolic pathways and compounds which accumulate in the symbiotic tissues. Studies on regulation of the overall process, and the control of enzyme activity in particular, are still fragmentary.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1987        PMID: 3120792     DOI: 10.1016/0300-9084(87)90176-3

Source DB:  PubMed          Journal:  Biochimie        ISSN: 0300-9084            Impact factor:   4.079


  8 in total

1.  Year-round monitoring of diversity and potential metabolic activity of the ectomycorrhizal community in a beech (Fagus silvatica) forest subjected to two thinning regimes.

Authors:  Marc Buée; Dominique Vairelles; Jean Garbaye
Journal:  Mycorrhiza       Date:  2004-06-25       Impact factor: 3.387

2.  Eucalypt NADP-dependent isocitrate dehydrogenase. cDNA cloning and expression in ectomycorrhizae.

Authors:  V Boiffin; M Hodges; S Gálvez; R Balestrini; P Bonfante; P Gadal; F Martin
Journal:  Plant Physiol       Date:  1998-07       Impact factor: 8.340

3.  Carbohydrate and Amino Acid Metabolism in the Ectomycorrhizal Ascomycete Sphaerosporella brunnea during Glucose Utilization : A C NMR Study.

Authors:  F Martin; M Ramstedt; K Söderhäll; D Canet
Journal:  Plant Physiol       Date:  1988-03       Impact factor: 8.340

4.  Carbohydrate and amino acid metabolism in the eucalyptus globulus-pisolithus tinctorius ectomycorrhiza during glucose utilization

Authors: 
Journal:  Plant Physiol       Date:  1998-10       Impact factor: 8.340

5.  Trees, fungi and bacteria: tripartite metatranscriptomics of a root microbiome responding to soil contamination.

Authors:  E Gonzalez; F E Pitre; A P Pagé; J Marleau; W Guidi Nissim; M St-Arnaud; M Labrecque; S Joly; E Yergeau; N J B Brereton
Journal:  Microbiome       Date:  2018-03-21       Impact factor: 14.650

6.  The genome of Rhizophagus clarus HR1 reveals a common genetic basis for auxotrophy among arbuscular mycorrhizal fungi.

Authors:  Yuuki Kobayashi; Taro Maeda; Katsushi Yamaguchi; Hiromu Kameoka; Sachiko Tanaka; Tatsuhiro Ezawa; Shuji Shigenobu; Masayoshi Kawaguchi
Journal:  BMC Genomics       Date:  2018-06-18       Impact factor: 3.969

7.  A "footprint" of plant carbon fixation cycle functions during the development of a heterotrophic fungus.

Authors:  Xueliang Lyu; Cuicui Shen; Jiatao Xie; Yanping Fu; Daohong Jiang; Zijin Hu; Lihua Tang; Liguang Tang; Feng Ding; Kunfei Li; Song Wu; Yanping Hu; Lilian Luo; Yuanhao Li; Qihua Wang; Guoqing Li; Jiasen Cheng
Journal:  Sci Rep       Date:  2015-08-11       Impact factor: 4.379

8.  Integrative Study Supports the Role of Trehalose in Carbon Transfer From Fungi to Mycotrophic Orchid.

Authors:  Jan Ponert; Jan Šoch; Stanislav Vosolsobě; Klára Čiháková; Helena Lipavská
Journal:  Front Plant Sci       Date:  2021-12-09       Impact factor: 5.753

  8 in total

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