Volford Bettina, Varga Mónika, Szekeres András, Kotogán Alexandra, Nagy Gábor, Vágvölgyi Csaba, Papp Tamás, Takó Miklós
Department of Microbiology, Faculty of Science and Informatics, University of Szeged, Közép fasor 52, H-6726 Szeged, Hungary.
MTA-SZTE "Lendület" Fungal Pathogenicity Mechanisms Research Group, University of Szeged, Közép fasor 52, H-6726 Szeged, Hungary.
J Fungi (Basel). 2021 Mar 19;7(3):229. doi: 10.3390/jof7030229.
β-Galactosidases of Mucoromycota are rarely studied, although this group of filamentous fungi is an excellent source of many industrial enzymes. In this study, 99 isolates from the genera , , , , and , were screened for their β-galactosidase activity using a chromogenic agar approach. Ten isolates from the best producers were selected, and the activity was further investigated in submerged (SmF) and solid-state (SSF) fermentation systems containing lactose and/or wheat bran substrates as enzyme production inducers. Wheat bran proved to be efficient for the enzyme production under both SmF and SSF conditions, giving maximum specific activity yields from 32 to 12,064 U/mg protein and from 783 to 22,720 U/mg protein, respectively. Oligosaccharide synthesis tests revealed the suitability of crude β-galactosidases from Szeged Microbiological Collection (SZMC) 11360 and SZMC 11025 to catalyze transgalactosylation reactions. In addition, the crude enzyme extracts had transfructosylation activity, resulting in the formation of fructo-oligosaccharide molecules in a sucrose-containing environment. The maximal oligosaccharide concentration varied between 0.0158 and 2.236 g/L depending on the crude enzyme and the initial material. Some oligosaccharide-enriched mixtures supported the growth of probiotics, indicating the potential of the studied enzyme extracts in future prebiotic synthesis processes.
毛霉亚门的β-半乳糖苷酶很少被研究,尽管这一类丝状真菌是许多工业酶的优良来源。在本研究中,使用显色琼脂法对来自根霉属、毛霉属、犁头霉属、脉孢菌属、曲霉属和青霉属的99个分离株进行了β-半乳糖苷酶活性筛选。从最佳产酶菌株中挑选出10个分离株,并在含有乳糖和/或麦麸底物作为酶生产诱导剂的深层发酵(SmF)和固态发酵(SSF)系统中进一步研究其活性。事实证明,麦麸在SmF和SSF条件下都有利于酶的生产,分别产生了32至12,064 U/mg蛋白质和783至22,720 U/mg蛋白质的最大比活性产量。寡糖合成试验表明,来自塞格德微生物保藏中心(SZMC)11360和SZMC 11025的粗β-半乳糖苷酶适合催化转半乳糖基化反应。此外,粗酶提取物具有转果糖基化活性,导致在含蔗糖的环境中形成低聚果糖分子。根据粗酶和初始原料的不同,最大寡糖浓度在0.0158至2.236 g/L之间变化。一些富含寡糖的混合物支持益生菌的生长,这表明所研究的酶提取物在未来益生元合成过程中具有潜力。