Stable isotope studies reveal pathways for the incorporation of non-essential amino acids in Acyrthosiphon pisum (pea aphids)

• Published in: Journal of experimental biology Vol. 218; no. Pt 23; pp. 3797 - 3806
• Main Authors: Haribal, Meena, Jander, Georg
• Format: Journal Article
• Language: English
• Published: England 01.12.2015
• Subjects: Amino Acids - metabolism; Animals; Aphids - metabolism; Asparagine - metabolism; Aspartic Acid - metabolism; Buchnera - metabolism; Carbon Isotopes; Glutamic Acid - metabolism; Glutamine - metabolism; Nitrogen - metabolism; Nitrogen Isotopes; Symbiosis; Glutamic acid; Buchnera aphidicola; Unbalanced diet; Asparagine; Endosymbiont; Aspartic acid; Biosynthesis; Aphid; Glutamine
• DOI: 10.1242/jeb.129189
• ISSN: 0022-0949

Plant roots incorporate inorganic nitrogen into the amino acids glutamine, glutamic acid, asparagine and aspartic acid, which together serve as the primary metabolites of nitrogen transport to other tissues. Given the preponderance of these four amino acids, phloem sap is a nutritionally unbalanced diet for phloem-feeding insects. Therefore, aphids and other phloem feeders typically rely on microbial symbionts for the synthesis of essential amino acids. To investigate the metabolism of the four main transport amino acids by the pea aphid (Acyrthosiphon pisum), and its Buchnera aphidicola endosymbionts, aphids were fed defined diets with stable isotope-labeled glutamine, glutamic acid, asparagine or aspartic acid (U-(13)C, U-(15)N; U-(15)N; α-(15)N; or γ-(15)N). The metabolic fate of the dietary (15)N and (13)C was traced using gas chromatography-mass spectrometry (GC-MS). Nitrogen was the major contributor to the observed amino acid isotopomers with one additional unit mass (M+1). However, there was differential incorporation, with the amine nitrogen of asparagine being incorporated into other amino acids more efficiently than the amide nitrogen. Higher isotopomers (M+2, M+3 and M+4) indicated the incorporation of varying numbers of (13)C atoms into essential amino acids. GC-MS assays also showed that, even with an excess of dietary labeled glutamine, glutamic acid, asparagine or aspartic acid, the overall content of these amino acids in aphid bodies was mostly the product of catabolism of dietary amino acids and subsequent re-synthesis within the aphids. Thus, these predominant dietary amino acids are not passed directly to Buchnera endosymbionts for synthesis of essential amino acids, but are rather are produced de novo, most likely by endogenous aphid enzymes.