Goyal Anna, Kalia Anu, Sodhi Harpreet Singh
Department of Microbiology, College of Basic Sciences and Humanities, Punjab Agricultural University, Ludhiana, Punjab, India.
EMN Laboratory, Department of Soil Science, College of Agriculture, Punjab Agricultural University, Ludhiana, Punjab, India.
Int J Med Mushrooms. 2018;20(12):1209-1221. doi: 10.1615/IntJMedMushrooms.2018028898.
Fruiting bodies of Ganoderma lucidum have been widely used as a source of potent nutraceutical products. However, the key proteins involved in fructifying G. lucidum, to our knowledge, have not yet been reported. We evaluated the protein profile of fruiting and nonfruiting G. lucidum strains at various developmental stages: mycelia, spawn running, pinning, and fruiting body. Four strains of G. lucidum (GL-I to GL-IV) were grown in both liquid medium (mushroom minimal medium broth) and bags of wheat straw, after which the biomass and fruiting bodies were harvested. Enzyme studies revealed enhanced intracellular and extracellular enzymatic activities during the spawn run stage compared with that during mycelial growth in broth. The esterase and peroxidase activities increased significantly during the pinning of the fruiting cultures, thus indicating their positive role in fructification. Fourier transform infrared spectroscopy of proteins at 3 stages of cultivation-spawn run, pin head formation, and fruiting-exhibited the presence of hydrophobic amino acids and an ordered protein structure in fruiting strains (GL-I and GL-II), indicating the presence of hydrophobin proteins and their role in mushroom fructification. However, basic and aromatic amino acids predominated in the nonfruiting strain GL-IV, and an unordered protein structure was present, which indicate the positive role of hydrophobic amino acids and hydrophobin proteins in mushroom fructification.
灵芝子实体已被广泛用作强效营养保健品的来源。然而,据我们所知,参与灵芝结实的关键蛋白质尚未见报道。我们评估了灵芝结实菌株和未结实菌株在不同发育阶段(菌丝体、发菌、现蕾和子实体阶段)的蛋白质谱。四株灵芝(GL-I至GL-IV)分别在液体培养基(蘑菇基本培养基肉汤)和麦秸袋中培养,之后收获生物量和子实体。酶学研究表明,与在肉汤中菌丝体生长阶段相比,发菌阶段的细胞内和细胞外酶活性增强。在结实培养物现蕾期间,酯酶和过氧化物酶活性显著增加,从而表明它们在结实过程中发挥了积极作用。对培养的三个阶段(发菌、针头形成和结实)的蛋白质进行傅里叶变换红外光谱分析,结果显示结实菌株(GL-I和GL-II)中存在疏水氨基酸和有序的蛋白质结构,表明存在疏水蛋白及其在蘑菇结实中的作用。然而,在未结实菌株GL-IV中,碱性和芳香族氨基酸占主导,且存在无序的蛋白质结构,这表明疏水氨基酸和疏水蛋白在蘑菇结实中发挥了积极作用。