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Tailoring fungal morphology of Aspergillus niger MYA 135 by altering the hyphal morphology and the conidia adhesion capacity: biotechnological applications

机译:通过改变菌丝形态和分生孢子粘附能力来定制黑曲霉MYA 135的真菌形态:生物技术应用

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摘要

Current problems of filamentous fungi fermentations and their further successful developments as microbial cell factories are dependent on control fungal morphology. In this connection, this work explored new experimental procedures in order to quantitatively check the potential of some culture conditions to induce a determined fungal morphology by altering both hyphal morphology and conidia adhesion capacity. The capacity of environmental conditions to modify hyphal morphology was evaluated by examining the influence of some culture conditions on the cell wall lytic potential of Aspergillus niger MYA 135. The relative value of the cell wall lytic potential was determined by measuring a cell wall lytic enzyme activity such as the mycelium-bound β-N-acetyl-D-glucosaminidase (Mb-NAGase). On the other hand, the quantitative value of conidia adhesion was considered as an index of its aggregation capacity. Concerning microscopic morphology, a highly negative correlation between the hyphal growth unit length (lHGU) and the specific Mb-NAGase activity was found (r = -0.915, P < 0.001). In fact, the environment was able to induce highly branched mycelia only under those culture conditions compatible with specific Mb-NAGase values equal to or higher than 190 U gdry.wt-1. Concerning macroscopic morphology, a low conidia adhesion capacity was followed by a dispersed mycelial growth. In fact, this study showed that conidia adhesion units per ml equal to or higher than 0.50 were necessary to afford pellets formation. In addition, it was also observed that once the pellet was formed the lHGU had an important influence on its final diameter. Finally, the biotechnological significance of such results was discussed as well.
机译:丝状真菌发酵的当前问题及其作为微生物细胞工厂的进一步成功发展取决于对照真菌的形态。在这方面,这项工作探索了新的实验程序,以便通过改变菌丝形态和分生孢子附着力来定量检查某些培养条件诱导确定的真菌形态的潜力。通过检查某些培养条件对黑曲霉MYA 135细胞壁裂解潜能的影响,评估了环境条件改变菌丝形态的能力。通过测量细胞壁裂解酶活性来确定细胞壁裂解潜能的相对值。例如结合菌丝体的β-N-乙酰基-D-氨基葡萄糖苷酶(Mb-NAGase)。另一方面,分生孢子粘附的定量值被认为是其聚集能力的指标。关于微观形态,发现菌丝生长单位长度(lHGU)和比Mb-NAGase活性之间高度负相关(r = -0.915,P <0.001)。实际上,只有在与等于或高于190 U gdry.wt -1 的特定Mb-NAGase值兼容的培养条件下,环境才能诱导高度分支的菌丝体。关于宏观形态,分生孢子粘附能力低,随后是菌丝散布。实际上,这项研究表明,每毫升分生孢子附着单位等于或高于0.50是形成小球所必需的。另外,还观察到一旦形成沉淀,lHGU对其最终直径具有重要影响。最后,还讨论了此类结果的生物技术意义。

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