产香真菌GS-1挥发性物质特征分析及抑菌作用观察

产香真菌GS—1为分离自构树枯枝的一株丛赤壳Nectria cinnabarina，该菌株产生浓郁的香味，其挥发性物质对多种重要植物病原菌均有明显的熏蒸抑制作用。为明确菌株GS—1挥发性物质对植物病原菌的熏蒸抑菌机制、挥发性物质化学组分及菌株生长过程中的挥发性物质释放量的动态规律，利用扫描和透射电镜观察GS—1菌株挥发性物质对灰葡萄孢菌丝和细胞结构的影响，通过HS—SPME法萃取产香真菌GS—1挥发性物质，并通过GC—MS进行挥发性物质释放时间规律的测定和组分鉴定。结果表明，菌株GS—1挥发性物质处理后，灰葡萄孢菌丝出现皱缩、畸形、顶端尖细等现象，同时细胞质含量减少且空腔增多。菌株GS—1挥发性物质释放量随培养时间的延长总体呈先升高后略降低逐渐趋于平稳的趋势，在第12 d达到最大峰值。从菌株GS—1挥发性物质中分离到34个化学组分，鉴定了其中18个组分，主要组分为[3S—（3α，3aβ，5α）]—1，2，3，3a，4，5，6，7—八氢—α，α，3，8—四甲基—5—薁甲醇、表荜澄茄油烯醇和α—广藿香烯，分别占挥发性物质总量34.22%、10.70%和5.60%。这些结果为菌株GS—1挥发性物质在植物病害防控中的合理开发和高效利用提供了理论依据。     

食用菌多糖抗运动疲劳研究进展

采用文献资料法对食用菌多糖抗运动疲劳的研究进展情况进行了研究。结果表明:食用菌多糖提取方法不同而食用菌多糖的提取率也不相同,超声波法+复合酶法及微波法提取食用菌多糖提取率较高,2种方法科学合理的结合提取食用菌多糖以及不同产地、品种和不同部位提取率是未来学者们需要研究的领域;目前,只是对极少部分食用菌多糖抗运动疲劳进行了研究,研究对象(动物)、模型、指标、评价单一而没有确定最佳剂量的时间而没确定的量。为此,提出了未来应加强和重视食用菌多糖抗疲劳运动多食用菌、多对象(尤其是人)、多模型、多指标、多评价、最佳剂量的研究以及量-效、构-效关系的研究建议。     

基于投入产出方法的食用菌产业生态补偿演化博弈研究

为了解决传统食用菌产业生态补偿演化博弈模型演化稳定性差的问题,提出基于投入产出方法的食用菌产业生态补偿演化博弈模型。依据食用菌产业实际情况,界定食用菌产业生态补偿利益相关者,引入投入产出方法,以此为基础,构建食用菌产业生态补偿演化博弈模型。以模型为工具,计算模型平衡点,并演化博弈食用菌产业生态补偿情况。仿真试验结果表明:与传统演化博弈模型相比,构建的食用菌产业生态补偿演化博弈模型极大的提升了演化稳定性,表现出了良好的演化博弈性能。     

基于食用菌主题的农业观光园规划设计思路

以食用菌主题观光园规划设计为研究对象,对农业观光园规划设计中食用菌进行简单介绍,并重点从观光旅游综合一体化园区规划设计的角度入手,探讨食用菌主题农业观光园规划设计思路。     

食用菌内源脂肪酸的研究

食用菌富含膳食纤维、矿物质、微量元素、维生素和多种氨基酸,是多功能理想食物。尽管食用菌脂类物质含量较低,但包含人类必需的不饱和脂肪酸,如亚油酸、油酸和亚麻酸等。通过对食用菌脂类物质研究成果进行总结,尤其是不饱和脂肪酸种类、含量及其开发利用,以期为食用菌的资源开发提供参考。     

Inhibiting fungus on largemouth bass eggs with copper sulfate and its toxicity to fry and juveniles

This study determined the effectiveness of copper sulfate (CuSO₄) to inhibit fungal growth (caused by Saprolegnia spp.) on largemouth bass (LMB) eggs spawned on/in fiber mats in very high-alkalinity/-hardness waters; experiments also determined the toxicity of CuSO₄ to LMB fry and juveniles. An untreated control and three CuSO₄ concentrations (10, 20, and 40 mg/L) were tested under a flow-through scenario in the effectiveness experiment. Eggs were treated daily until hatching began. Fungal load at the time of hatch had a total area > 3.0 cm² in the untreated controls, total area 1.0 to <2.0 cm² in the 10 and 20 mg/L CuSO₄ treatments, and total area > 1.0 cm² in the 40 mg/L CuSO₄ treatments. Fungus samples were identified as Saprolegnia australis. The 24-hr median lethal concentration (LC50) values on the LMB yolk-sac and swim-up fry were 32.0 and 4.6 mg/L CuSO₄, respectively; the No Observed Effect Concentrations (NOEC) were 16.0 and 0.125 mg/L CuSO₄, respectively. Juvenile LMB were extremely tolerant to CuSO₄, and their 24-hr LC50 value was 185.5 mg/L; the NOEC was 64 mg/L. This study indicates that CuSO₄ can be an important resource for hatcheries to control egg fungus, especially in high-alkalinity/-hardness waters.     

食用菌菌包生产现状与发展趋势

介绍了食用菌栽培工艺流程及菌包生产国内外研究现状，指出存在的问题及改进措施，并提出食用菌工厂化生产的发展趋势。      

New Polyketides from the Antarctic Fungus Pseudogymnoascus sp. HSX2#-11

The species Pseudogymnoascus is known as a psychrophilic pathogenic fungus with a ubiquitous distribution in Antarctica. Meanwhile, the study of its secondary metabolites is infrequent. Systematic research of the metabolites of the fungus Pseudogymnoascus sp. HSX2#-11, guided by the method of molecular networking, led to the isolation of one novel polyketide, pseudophenone A (1), along with six known analogs (2–7). The structure of the new compound was elucidated by extensive spectroscopic investigation and single-crystal X-ray diffraction. Pseudophenone A (1) is a dimer of diphenyl ketone and diphenyl ether, and there is only one analog of 1 to the best of our knowledge. Compounds 1 and 2 exhibited antibacterial activities against a panel of strains. This is the first time to use molecular networking to study the metabolic profiles of Antarctica fungi.     

A fluorescence‐based assay for in vitro screening of Saprolegnia inhibitors

The incidence of fish pathogenic oomycetes, Saprolegnia, has increased significantly in aquaculture since the ban of malachite green. For the efficient characterization of anti‐Saprolegnia therapeutics, simple accurate methods are required. However, the current screening methods are limited by time, and none of them are confirming the viability of treated spores or hyphae. In this study, a modified fluorescence‐based assay for the in vitro screening of Saprolegnia inhibitors has been developed. This method involves the use of FUN‐1 viability dye combined with calcofluor white M2R, and is based on the formation of orange‐red cylindrical intravacuolar structures (CIVS) in metabolically active spores, hyphae and biofilms. Heat‐killed and bronopol‐treated Saprolegnia spores, hyphae and biofilms exhibited diffuse bright green fluorescence which confirms complete loss of viability. For boric acid‐treated spores, no germination was observed. However, tiny CIVS were observed in 50% of treated spores which indicated reduction in their viability. Our results proved that FUN‐1 dye is an efficient tool to distinguish between live and dead Saprolegnia spores, hyphae and biofilms and to monitor the change in Saprolegnia viability during qualitative evaluation of potential anti‐Saprolegnia compounds.