真菌表面结构的研究

I. Tani, M. Kuriyama, T. Otsuka
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引用次数: 1

摘要

许多真菌的细胞壁含有几丁质,一种n -乙酰氨基葡萄糖的聚合物。在一项有关真菌表面结构的研究过程中,对许多真菌全细胞及其纯化细胞壁进行了分析,以测量其几丁质含量。本文报道了几种真菌中甲壳素含量的定量分析结果,以及几种真菌对苯酚的敏感性随孵育时间(4-20天)的变化与甲壳素含量的关系。结果表明:1)甲壳素水解得到的盐酸氨基葡萄糖与标准盐酸氨基葡萄糖具有相同的吸收曲线,在530mm处有不同的最大值;本实验选用4株真菌(黑曲霉IAM 2020、白地霉IFO 6454、青霉菌IFO 4626、红毛霉IFO 5467)。分别在合成培养基和Sabouraud培养基中振荡培养4、8、12、16和20 d,定量测定干燥全细胞和纯化细胞壁的几丁质含量。随着孵育时间的增加,甲壳素含量逐渐增加。此外,还测定了用声波处理获得的纯化细胞壁制剂中所有真菌菌株8和16 d培养物的几丁质含量。用荧光显微镜、相衬显微镜和电子显微镜等多种显微方法检测细胞壁的纯度。结果如图3、图4、图1、图2、表1.3所示。)在真菌培养4-20天的时间内,估计培养基pH值的变化和培养滤液乙醇沉淀的干重。结果如图5和表2.4所示)在不考虑培养年龄和甲壳素含量的情况下,两种真菌(a.niger IAM 2020, g.c addum IFO 6454)对苯酚的敏感性没有变化。结果如表3所示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Studies on the Surface Structure of Fungi
The cell wall of many fungi contains chitin a polymer of N-acetylglucosamine. During the course of a study concerned with the surface structure of fungi, a number of fungal whole cells and their purified cell walls were analysed to measure their chitin contents. This report presents the results of quantitative analyses of chitin in several fungi and their susceptibility to phenol in relation to the changes of chitin content followed by the length of incubation (4-20 days).The results are as follows.1) Both the glucosamine hydrochloride obtained by hydrolysis of the chitin and standard D-glucosamine hydrochloride revealed identical absorption curves showing a distinct maximum value at 530mμ. The results are shown in Fig. 2.2) For this experiment, 4 fungal strains (Asperillus niger IAM 2020, Geotrichum candidum IFO 6454, Penicillium chrysogenum IFO 4626, Trichophyton rubrum IFO 5467) were used. Chitin contents of dry whole cell and purified cell wall were estimated quantitatively on each of 4, 8, 12, 16 and 20 daycultures which were grown in either synthetic or Sabouraud's medium by shaking culture. It was found that the chitin content increased gradually with the day of incubation. In addition to this, the chitin contents of 8 and 16 days old culture of all fungal strains were determined in purified preparations of cell walls which were obtained by means of sonic treatment. The purity of the cell wall was examined with several microscopic methods, such as fluorescence microscopy, phase-contrast microscopy and electron microscopy. The results are shown in Figs. 3 and 4, Photos 1 and 2 and Table 1.3) During 4-20 days incubation time of fungi, the changes of pH in the medium and the dry weight of ethanol precipitate of culture filtrate were estimated. The results are shown in Fig. 5 and Table 2.4) Without regard to the age of cultures or their chitin content, the susceptibility to phenol of two fungi (i.e. A. niger IAM 2020, G. candidum IFO 6454) was not changed. The results are shown in Table 3.
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