Bel Yolanda, Rodríguez-Gómez Amador, Bielza Pablo, Ferré Juan
Laboratory of Biotechnological Control of Pests, Institute of Biotechnology and Biomedicine (BIOTECMED), Universitat de València, Burjassot, 46100 València, Spain.
Departament of Genetics, Universitat de València, Burjassot, 46100 València, Spain.
Insects. 2025 Jul 23;16(8):756. doi: 10.3390/insects16080756.
Nymphs of the mutant of (Fieber) are orange-colored instead of the yellowish color of the wild-type individuals. Since there were no previous studies of the pigments of this species, we searched for differences in pigments of the pteridine family between both strains. Fluorescent compounds from nymph extracts were separated by cellulose thin-layer chromatography (TLC) and by size exclusion chromatography, followed by LC/MS/MS. The present study has allowed the identification for the first time in of erythropterin, leucopterin, 7-methylxanthopterin, xanthopterin, isoxanthopterin, pterin, and biopterin. The quantification was performed by fluorometry after elution of the pteridines previously separated by TLC. The results showed that the orange color in the nymphs was due to the accumulation of the orange pigment erythropterin. Additionally, mutant nymphs exhibited significantly elevated levels of pterin and reduced levels of leucopterin. The possibility that these differences were due to differences in xanthine dehydrogenase (XDH) activity was tested; the results indicated that XDH deficiency is unlikely to be responsible for the mutant phenotype. Considering that the mutation is recessive, the mutant phenotype should, most likely, be due to a disruption in downstream metabolic steps involved in erythropterin processing.
(费伯)突变体的若虫是橙色的,而不是野生型个体的淡黄色。由于此前没有对该物种色素的研究,我们寻找了两个品系之间蝶啶家族色素的差异。若虫提取物中的荧光化合物通过纤维素薄层色谱(TLC)和尺寸排阻色谱进行分离,随后进行液相色谱/串联质谱分析。本研究首次在[具体物种]中鉴定出了红蝶呤、白蝶呤、7-甲基黄蝶呤、黄蝶呤、异黄蝶呤、蝶呤和生物蝶呤。通过对先前经TLC分离的蝶啶洗脱后的荧光测定法进行定量。结果表明,[具体物种]若虫的橙色是由于橙色色素红蝶呤的积累。此外,突变体若虫的蝶呤水平显著升高,白蝶呤水平降低。测试了这些差异是否由于黄嘌呤脱氢酶(XDH)活性差异所致;结果表明,XDH缺乏不太可能是突变体表型的原因。考虑到[具体物种]突变是隐性的,突变体表型很可能是由于红蝶呤加工过程中下游代谢步骤的中断所致。