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Plant-Microorganism Interactions

Arbuscular mycorrhizal fungi enhances salinity tolerance of Panicum turgidum Forssk by altering photosynthetic and antioxidant pathways

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Pages 230-242 | Received 24 Feb 2015, Accepted 13 May 2015, Published online: 27 Aug 2015

Figures & data

Figure 1. (a–i) Morphology of typical an intact crushed spores of AMF. (a, b, c) C. etunicatum (syn. G. etunicatum); (d, e, f) F. mosseae (syn. G. mosseae); (g, h, i), R. intraradices (syn. G. intraradices).

Figure 1. (a–i) Morphology of typical an intact crushed spores of AMF. (a, b, c) C. etunicatum (syn. G. etunicatum); (d, e, f) F. mosseae (syn. G. mosseae); (g, h, i), R. intraradices (syn. G. intraradices).

Figure 2. The colonization of AMF in the roots of P. turgidum. (a): vesicle (V) and spore (S) occurrence of the AMF-colonized root section, (b): Vesicles (V) formed in roots of P. turgidum, (c): Hyphae (H) and hyphal coils (HC) in roots of P. turgidum, (d): colonization of plant roots by AMF hyphae (H), vesicles (V) and spore density (S), (e): The root segments colonized by arbuscles (A), trank (T) and hyphae (H) of AMF, (f): Arbuscles (A), and hyphae (H) colonize the root.

Figure 2. The colonization of AMF in the roots of P. turgidum. (a): vesicle (V) and spore (S) occurrence of the AMF-colonized root section, (b): Vesicles (V) formed in roots of P. turgidum, (c): Hyphae (H) and hyphal coils (HC) in roots of P. turgidum, (d): colonization of plant roots by AMF hyphae (H), vesicles (V) and spore density (S), (e): The root segments colonized by arbuscles (A), trank (T) and hyphae (H) of AMF, (f): Arbuscles (A), and hyphae (H) colonize the root.

Table 1. Effect of NaCl (250 mM) on total spores (spore/50 g soil) and structural colonization (%) of AMF in P. turgidum.

Table 2. Effect of NaCl (250 mM) in presence and absence of AMF on photosynthetic pigment contents (mg/g fresh weight) in P. turgidum.

Figure 3. (a)–(d). The effect of NaCl (250 mM) in presence and absence of AMF on (a) superoxide dismutase (SOD), (b) catalase (CAT), (c) peroxidase (POD) and (d) glutathione reductase (GR) (EU mg−1 protein) activities in P. turgidum.

Figure 3. (a)–(d). The effect of NaCl (250 mM) in presence and absence of AMF on (a) superoxide dismutase (SOD), (b) catalase (CAT), (c) peroxidase (POD) and (d) glutathione reductase (GR) (EU mg−1 protein) activities in P. turgidum.

Figure 4. (a)–(f) Effect of NaCl (250 mM) in presence and absence of AMF on activities of carbon metabolizing enzymes (μmol/mg chlorophyll/min) in P. turgidum. (a) pyruvate orthophosphate dikinase; (b) phosphoenolpyruvate carboxylase; (c) NADP-malate dehydrogenase; and (d) NAD-malate dehydrogenase; (e) NADP-malic enzyme and (f) Rubisco.

Figure 4. (a)–(f) Effect of NaCl (250 mM) in presence and absence of AMF on activities of carbon metabolizing enzymes (μmol/mg chlorophyll/min) in P. turgidum. (a) pyruvate orthophosphate dikinase; (b) phosphoenolpyruvate carboxylase; (c) NADP-malate dehydrogenase; and (d) NAD-malate dehydrogenase; (e) NADP-malic enzyme and (f) Rubisco.

Table 3. Effect of NaCl (250 mM) in presence and absence of AMF on systemic resistance attributes [H2O2 (μMol/g fresh weight), MDA (nMol/g fresh weight), TP (mg/g fresh weight), GB (μMol/g fresh weight), and proline (μMol/g fresh weight) in P. turgidum.

Table 4. Effect of NaCl (250 mM) in presence and absence of AMF on sugars content (mg glucose/g dry weight) in P. turgidum.

Table 5. Effect of NaCl (250 mM) in presence and absence of AMF on ion accumulation (mg/g dry weight) in P. turgidum.