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Diversity of Varthemia candicans phytochemicals in response to growth habitat

Abstract Aerial parts of Varthemia candicans were collected seasonally for one year (winter, spring, summer and autumn) from Wadi Habbes (rocky habitat) and Sand Dunes habitat, West Marsa Matrouh, Egypt. The results of the plant photochemical analysis cleared out that the amount of soluble carbohydrates in the study habitats during the wet seasons (winter and autumn) was higher than that of the dry season, however the content of insoluble carbohydrates recorded a reverse trend. HPLC analysis of free sugars detected the occurrence of glucoronic acid, raffinose, glucose, galactose, fructose and fucose. The most abundant free sugar in WH was glucoronic acid but in SD was raffinose. Also, HPLC analysis of combined sugars detected the presence of glucose, mannose, fructose and maltose with the commonness of maltose in the two study habitats. The amount of soluble amino acids and soluble proteins were greater in SD habitat than WH habitat during all seasons, except autumn season. Free amino acids in WH habitat revealed the richness of the plant with asparagines, but in SD habitat with proline, but in case of protein amino acids proline was common in WH and aspartic acid was common in SD habitat. The total lipids content was greater in SD habitat than in WH. GC-MS analysis of fatty acids revealed that Hexadecanoic acid methyl ester was common in the plant aerial parts in WH habitat, however the fatty acid 6-Acetyl-8methoxy-2,2-dimethyl-2H-chromen-5-ol was common in the plant aerial parts in SD habitat.

Abstract Aerial parts of Varthemia candicans were collected seasonally for one year (winter, spring, summer and autumn) from Wadi Habbes (rocky habitat) and Sand Dunes habitat, West Marsa Matrouh, Egypt. The results of the plant photochemical analysis cleared out that the amount of soluble carbohydrates in the study habitats during the wet seasons (winter and autumn) was higher than that of the dry season, however the content of insoluble carbohydrates recorded a reverse trend. HPLC analysis of free sugars detected the occurrence of glucoronic acid, raffinose, glucose, galactose, fructose and fucose. The most abundant free sugar in WH was glucoronic acid but in SD was raffinose. Also, HPLC analysis of combined sugars detected the presence of glucose, mannose, fructose and maltose with the commonness of maltose in the two study habitats. The amount of soluble amino acids and soluble proteins were greater in SD habitat than WH habitat during all seasons, except autumn season. Free amino acids in WH habitat revealed the richness of the plant with asparagines, but in SD habitat with proline, but in case of protein amino acids proline was common in WH and aspartic acid was common in SD habitat. The total lipids content was greater in SD habitat than in WH. GC-MS analysis of fatty acids revealed that Hexadecanoic acid methyl ester was common in the plant aerial parts in WH habitat, however the fatty acid 6-Acetyl-8methoxy-2,2-dimethyl-2H-chromen-5-ol was common in the plant aerial parts in SD habitat.

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J. Bio. & Env. Sci. 2014<br />

Pho<strong>to</strong>gram 2. Comb<strong>in</strong>ed sugars (%) <strong>of</strong> the aerial parts <strong>of</strong> V. <strong>candicans</strong> <strong>in</strong> the study <strong>habitat</strong>s us<strong>in</strong>g HPLC<br />

technique.<br />

The plant grow<strong>in</strong>g <strong>in</strong> WH <strong>habitat</strong> was characterized<br />

by the presence <strong>of</strong> three comb<strong>in</strong>ed monosugars<br />

glucose and the disaccharide mal<strong>to</strong>se <strong>in</strong> the plant <strong>in</strong><br />

the two <strong>habitat</strong>s, <strong>in</strong> addition <strong>to</strong> the two<br />

monosaccharides mannose and fruc<strong>to</strong>se <strong>in</strong> the plant<br />

<strong>of</strong> WH <strong>habitat</strong>. The most abundant comb<strong>in</strong>ed sugar <strong>in</strong><br />

the plant aerial parts <strong>in</strong> this <strong>habitat</strong> was the<br />

disaccharide mal<strong>to</strong>se (96.5%), while the most<br />

<strong>in</strong>adequate sugar was the monosaccharide fruc<strong>to</strong>se<br />

(0.3%). However, the plant grow<strong>in</strong>g <strong>in</strong> SD <strong>habitat</strong> was<br />

characterized by lower number <strong>of</strong> comb<strong>in</strong>ed sugars,<br />

one comb<strong>in</strong>ed monosaccharide; glucose (14.2%) and<br />

one disaccharide, mal<strong>to</strong>se (85.8%). The data revealed<br />

that the two monosaccharides mannose and fruc<strong>to</strong>se<br />

have been vanished <strong>in</strong> SD <strong>habitat</strong>, so the plant<br />

compensated the deficiency <strong>of</strong> these two sugars by the<br />

abundance <strong>of</strong> the monosaccharide glucose.<br />

Li et al. (2013) found a slight <strong>in</strong>crease <strong>in</strong> soluble sugar<br />

concentration <strong>in</strong> Eremospar<strong>to</strong>n songoricum with the<br />

<strong>in</strong>crease <strong>in</strong> the osmotic potential. They reported that<br />

one <strong>of</strong> the osmotic stress defense mechanisms is the<br />

accumulation <strong>of</strong> organic osmolytes (such as prol<strong>in</strong>e,<br />

soluble sugars, glyc<strong>in</strong>e beta<strong>in</strong>e, and organic acids) <strong>in</strong><br />

the cy<strong>to</strong>plasm <strong>to</strong> ma<strong>in</strong>ta<strong>in</strong> the plant water potential<br />

dur<strong>in</strong>g drought stress. The severity <strong>of</strong> drought is<br />

unpredictable as it depends on many fac<strong>to</strong>rs such as<br />

occurrence and distribution <strong>of</strong> ra<strong>in</strong>fall, evaporative<br />

demands and moisture s<strong>to</strong>r<strong>in</strong>g capacity <strong>of</strong> soils (Wery<br />

et al., 1994). One <strong>of</strong> the most common stress<br />

<strong>to</strong>lerance strategies <strong>in</strong> plants is the overproduction <strong>of</strong><br />

different types <strong>of</strong> compatible organic solutes (Serraj<br />

and S<strong>in</strong>clair, 2002). S<strong>in</strong>gh (2004) proved that a<br />

greater accumulation <strong>of</strong> sugar lowers the osmotic<br />

potential <strong>of</strong> cells and reduces loss <strong>of</strong> turgidity <strong>in</strong><br />

plants. The other possible role <strong>of</strong> sugar may be as a<br />

readily available energy source.<br />

Soluble am<strong>in</strong>o acids and soluble prote<strong>in</strong> contents<br />

Data <strong>in</strong> Table (3) represent the variation <strong>in</strong> soluble<br />

am<strong>in</strong>o acids and soluble prote<strong>in</strong> contents <strong>in</strong> V.<br />

<strong>candicans</strong> aerial parts dur<strong>in</strong>g the study seasons <strong>in</strong> the<br />

studied <strong>habitat</strong>s (WH and SD). The variation <strong>in</strong> the<br />

contents <strong>of</strong> soluble am<strong>in</strong>o acids and soluble prote<strong>in</strong>s<br />

varied statistically with highly significant value<br />

(P

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