| Issue |
BIO Web Conf.
Volume 23, 2020
II International Scientific Conference “Plants and Microbes: The Future of Biotechnology” (PLAMIC2020)
|
|
|---|---|---|
| Article Number | 02011 | |
| Number of page(s) | 6 | |
| Section | Microbial Biotechnology | |
| DOI | https://doi.org/10.1051/bioconf/20202302011 | |
| Published online | 14 August 2020 | |
Structural lipids and carbohydrates of the deep mycelium of phoma-like micromycetes, potential mycoherbicides
1 All-Russian Institute of Plant Protection, Laboratory of Toxicology and Biotechnology, 196608 Saint Petersburg, Russia
2 Saint-Petersburg State Institute of Technology, Department of Molecular Biotechnology, 190013 Saint Petersburg, Russia
3 Saint Petersburg State University, Research park, Centre for Molecular and Cell Technologies, 199034 Saint Petersburg, Russia
* Corresponding author: svsokornovs@vizr.spb.ru
The work is devoted to the mycelium biochemical composition of Stagonospora cirsii C-211, Calophoma complanata 32.121, Didymella macrostoma 32.52. These phylogenetically distant species of phoma-like micromycetes are the potential mycoherbicides of Cirsium arvense, Heracleum sosnowskyi, and Convolvulus arvensis, respectively. The S. cirsii C-211, C. complanata 32.121, D. macrostoma 32.52 mycelium in the early stationary growth phase was obtained on sucrose-soybean nutrient medium. It was shown that the lipid and carbohydrate (polyols, sugars) profiles of these strains have much in common. We suppose that levels of arabitol and trehalose influence to the stress-resistant of phoma-like micromycetes. In particularly, these carbohydrates serve structural and protective roles in the cell walls during osmotic and temperatures stress. The ratio of phosphatidylcholine to phosphatidylethanolamine and the proportion of phosphatidylserine among structural lipids also determine the properties of mycelium, and can be used to assess its quality.
© The Authors, published by EDP Sciences, 2020
This is an Open Access article distributed under the terms of the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
1 Introduction
Phytopathogenic phoma-like micromycetes can be used as a basis for the development of mycoherbicides for managing troublesome invasive grasses and worst weeds. An example is Phoma macrostoma (=Didymella macrostoma) strain 94-44B. Registered in Canada and the USA anti-broadleaf weeds bioherbicide were developed based on mycelium, spores and metabolites of this strain [1]. Phoma-like micromycetes are heterogeneous group of fungi formed by their morphological and cultural peculiarities. In this paper, we consider three phylogenetically distant species of phoma-like fungi belonging to different genera, including a strain of the same species Phoma macrostoma as in a commercial mycoherbicide. Two other strains of S. cirsii C-211, C. complanata 32.121, are positioned as potential mycoherbicides of Cirsium arvense and Heracleum sosnowskyi [2-3]. Recently, publications on the biochemistry of phytopathogenic micromycetes have reappeared. This is due to the fact that the quantitative and qualitative composition of structural lipids, free amino acids and carbohydrates (polyols and sugars) often allows us to predict the viability of pathogens (in the field conditions, during the stabilize organisms, distribution and storage), their resistance to stress-factors (drying up, UV, high and low temperatures), etc. For example, bioprotective effects of trehalose and polyols was shown [4]. In turn, structural lipids are responsible for fluidity, structure and durability membrane, cell signaling and adaptation process [5-7]. The aim of this work was a biochemical analysis of the deep mycelium S. cirsii C-211, C. complanata 32.121, D. macrostoma 32.52.
2 Materials and methods
Calophoma complanata 32.121 and Didymella macrostoma 32.52 strains from the Laboratory of Mycology and Phytopathology pure culture collection and Stagonospora cirsii C-211 from the Laboratory of Toxicology and Biotechnology collection of the All-Russian Institute of Plant Protection was used. The strains of S. cirsii C-211 was isolated from necrotic leaf lesions of Cirsium arvense, C. complanata 32.121 was isolated from Heracleum sibiricum, and D. macrostoma 32.52 was isolated from Convolvulus arvensis.
The sucrose-soybean growth medium contained sucrose 30 g/1, soy flour 14 g/1, KH2PO4 1 g/, MgSO4×7H2O 0.5 g/ 1. The mycelium was obtained by submerged cultivation during 144 h on an orbital shaker at 180 rpm at 24°C. The deep mycelium was harvest in the early stationary growth phase.
The extraction of structural lipids was carried out according to Bligh, Dyer (1959) [8] with modifications [9]. High performance thin layer chromatography (HPTLC) was used to determine structural lipid profiles. The mobile phases were solutions containing chloroform: methanol: water: ammonia (24%) 60:34:4:2 w/w. The developed plates were dried Once the spots have been visualized by the copper sulfate solution (20 g CuSO4, 200 ml methanol, 8 ml H2SO4, 8 ml H3PO4) with heating, the plates were scanned at 550 nm. Samples and standards were compared by Rf values and colors [10].
The extraction of carbohydrates mycelium was carried out by 80% ethanol at 80°C for 1 h. The alcohol extracts were concentrated in a rotary evaporator with vacuum controller at 40°C. The dried fractions were then redissolved in pyridine to obtain silyl derivatives which were analyzed by GC-MS according to Sokornova et al. [11].
The analysis of sugars in the ethanol extract of mycelium was performed by the HPTLC according to Sokornova et al. [12].
The experience was repeated 2 times, in at least 4 replications per variant. The data obtained was processed by analysis of variance. The difference significance assessment between the means was assessed by the smallest significant difference (HCP0.05).
3 Results and discussion
A biochemical analysis of the S. cirsii C-211, C. complanata 32.121, D. macrostoma 32.52 mycelium at the beginning of the stationary growth phase was carried out. It has been shown previously that the similar mycelium of S. cirsii is most resistant to drying [3].
The mycopesticides disadvantages include instability field efficacy, the difficulty of stabilizing propagules and the limited shelf life of the formulations. It is known that sugars, in particular trehalose, are the most effective cryoprotectants during drying or freezing. Their action is due to a slowdown in the rate of change of the lipid phase under extreme conditions, which maintains the integrity and function of the membrane [13]. In turn, the protective effect of polyols is associated with a decrease the temperature of freezing, support for osmotic pressure and protection of enzymes from adverse effects [14]. In the study we analyzed the content of lipids and carbohydrates in the mycelium of phoma-like fungi.
3.1 Phospholipids profiles of phoma-like micromycetes
The mycelium of phoma-like fungi had, in almost all cases, a typical for mycromicetes phospholipid profile [15]. The main lipid classes were phosphatidylcholine (PC) and phosphatidylethanolamine (PE), whose percentage of the mycelium structural lipids was 58.0 ± 3.2, 64.5 ± 4.0 and 65.8 ± 3.8 for S. cirsii C-211, C. complanata 32.121, D. macrostoma 32.52, respectively (Fig. 1). According to available data, that the ratio of these phospholipids, along with phosphatidylserine (PS) and ergosterol determines the adaptive properties of fungal membranes [7]. For S. cirsii C-211, C. complanata 32.121, D. macrostoma 32.52 mycelium of the same age, there was no significant difference in the ratio of PC to PE, it was 1.4, 1.5, and 1.5, respectively. In the same variants there were significant differences, however, between PS level (10.0 ± 2.8, 3.7 ± 2.2, and 7.5 ± 2.6 %) (Fig. 1). A sufficiently high level of phosphatidic acid (PA) was found in the S. cirsii C-211 and C. complanata 32.121. It should be noted that PA is a secondary messenger of eukaryotic cell processes. The strains were not different about phosphatidylinositol (PI) and glycoceramides (GlCer) levels.
Thus, we suppose, an evaluation of PS level makes it possible to characterization mycelium and thus its environmental impact stability.
 |
Fig. 1 The content of structural lipids in the mycelium of phoma-like micromycetes, LSD0.05=2.8 |
3.2 Carbohydrate profiles of phoma-like micromycetes
Disaccharides (trehalose, sucrose, mannose) and polyols (mannitol, arabitol, glycerol) accumulation is one of the several mechanisms employed by phoma-like fungi to cope with biotic and abiotic stress [16]. Often, the accumulation of intracellular polyols occurs in the stationary phase of growth. Also, carbohydrates are reserves of carbon and energy, mobilized during regrowth [17].
The amount of total polyol pool of S. cirsii C-211, C. complanata 32.121, D. macrostoma 32.52 mycelium was 9.4 ± 0.8, 9.2 ± 0.9, 10.8 ± 0.9 mg / g. For all species the major polyols were arabitol and mannitol. The S. cirsii C-211 and C. complanata 32.121 mycelium contained much more myo-inositol and erythritol than D. macrostoma 32.52 mycelium (Fig. 2). It is important to emphasize that phosphorylated myo-inositol is actively involved in the regulation of fungal development in response to stress [18]. In turn D. macrostoma 32.52 differed from other analyzed species in a rather high glycerol and sorbitol levels (1.2 ± 0.8 mg / g and 2.0 ± 0.8 mg / g, respectively).
The sugar profile of S. cirsii C-211, C. complanata 32.121 and D. macrostoma 32.52 mycelium showed that the major sugars are disaccharide trehalose and monosaccharides glucose and fructose. As in the case of polyols, the sugar pool of D. macrostoma 32.52 mycelium had some features. However, the trehalose and glucose levels did not differ significantly (Fig.3).
 |
Fig. 2 Polyols contents in the mycelium of phoma-like micromycetes, LSD0.05=0.9 |
 |
Fig. 3 Sugar contents in the mycelium of phoma-like micromycetes, LSD0.05=1.2 |
4 Conclusion
Thus, the phoma-like fungi had a very similar phospholipids and carbohydrates pools. It was previously shown that the accumulation of arabitol and trehalose correlates with the development of S. cirsii C-163 mycelium [11-12]. We suppose that levels of arabitol and trehalose influence to the stress-resistant of phoma-like micromycetes. In particularly, these carbohydrates serve structural and protective roles in the cell walls during osmotic and temperatures stress. The ratio of phosphatidylcholine to phosphatidylethanolamine and the proportion of phosphatidylserine among structural lipids also determine the properties of mycelium, and can be used to assess its quality.
This work was supported by RNF grant 16-16-00085. The authors acknowledge Centre for Molecular and Cell Technologies of Saint-Petersburg State University.
References
- Pest Management Regulatory Agency, Label Search (www.hc-sc.gc.ca/cpsspc/pest/index-eng.php) [Google Scholar]
- E.L. Gasich, L.B. Khlopunova, A.O. Berestetskiy, S.V. Sokornova, Patent Russian Federation No. 2439141 C1 Strain of fungi Phoma complanata (Tode) Desm 1,40 (AIPP) mycoherbicidal active against hogweed Sosnowski (2010) [Google Scholar]
- N.A. Pavlova, S.V. Sokornova, Plant Protection News 4, 67 (2018). DOI:10.31993/2308-6459-2018-4(98)-67-69 [CrossRef] [Google Scholar]
- L.M. Crowe, CBPA 131, 505 (2002). DOI:10.1016/S1095-6433(01)00503-7 [Google Scholar]
- G. van Meer, D.R. Voelker, G.W. Feigenson, Nat. Rev. Mol. Cell Biol. 9, 112 (2008). DOI:10.1038/nrm2330 [CrossRef] [PubMed] [Google Scholar]
- J. Wang, H. Wang, C. Zhang, T. Wu, Z. Ma, Y. Chen, Phytopathol. Research 1, 16 (2019). DOI:10.1186/s42483-019-0023-9 [CrossRef] [Google Scholar]
- P. Perczyk, A. Wójcik, P. Wydro, M. Broniatowski, BBA 1862, 183136 (2020). DOI:10.1016/j.bbamem.2019.183136 [CrossRef] [Google Scholar]
- E.G. Bligh, W.J. Dyer, Can. J. Biochem. Physiol. 37, 911 (1959) [Google Scholar]
- L. Li, J. Han, W. Zhenpeng, J. Liu, J. Wei, S. Xiong, Z. Zhao, Int. J. Mol. Sci. 15, 10492 (2014). DOI:10.3390/ijms150610492 [Google Scholar]
- G.M. Frolova, S.V. Sokornova, A.O. Berestetskiy, Appl. Biochem. Microbiol. 55, 556 (2019). DOI:10.1134/S0003683819050041 [Google Scholar]
- S. Sokornova, G. Frolova, A. Shavarda, N. Pavlova, A. Berestetskiy, BIO Web of Conf. 18, (2020). DOI:10.1051/bioconf/20201800028 [Google Scholar]
- S. Sokornova, M. Gomzhina, E. Gasich, I. Merkoulov, D. Aman, G. Frolova, A. Radaev, A. Berestetskiy, BIO Web of Conf. 18, (2020). DOI:10.1051/bioconf/20201800027 [Google Scholar]
- A.D. Brown, Adv. Microbial. Physiol. 17, 181 (1978). DOI:10.1016/S0065-2911(08)60058-2 [CrossRef] [Google Scholar]
- L.M. Crowe, C. Womersley, J.H. Crowe, D. Reid, L. Appel, A. Rudolph, BBA-Biomembranes 861, 131 (1986). DOI:10.1016/0005-2736(86)90411-6 [CrossRef] [Google Scholar]
- A.I.P.M de Kroon, P.J. Rijken, C.H. De Smet, Prog. Lipid Res. 52, 374 (2013). DOI:10.1016/j.plipres.2013.04.006 [CrossRef] [PubMed] [Google Scholar]
- L.M. Crowe, Comp. Biochem. Physiol. A Mol. Integr. Physiol. 131, 505 (2002). DOI:10.1016/s1095-6433(01)00503-7 [CrossRef] [PubMed] [Google Scholar]
- H. Kumdam, S.N. Murthy, S.N. Gummadi, IJSAR 1, 1 (2014) [Google Scholar]
- V.A. Morrissette, R.J. Rolfes, Current genetics (2020). DOI:10.1007/s00294-020-01078-8 [Google Scholar]
All Figures
|
Fig. 1 The content of structural lipids in the mycelium of phoma-like micromycetes, LSD0.05=2.8 |
| In the text | |
|
Fig. 2 Polyols contents in the mycelium of phoma-like micromycetes, LSD0.05=0.9 |
| In the text | |
|
Fig. 3 Sugar contents in the mycelium of phoma-like micromycetes, LSD0.05=1.2 |
| In the text | |
Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.
Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.
Initial download of the metrics may take a while.