首页|大球盖菇液体菌种繁育工艺研究

大球盖菇液体菌种繁育工艺研究

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[目的]优化大球盖菇液体菌种培养基,探究液体培养过程中的生长规律,确立液体菌种繁育栽培种工艺参数。[方法]以大球盖菇 8号为试验菌株,以菌丝体生物量为评价指标,采用单因素和正交试验L9(34)优化液体菌种培养基。测定液体菌种菌丝体生物量,还原糖和氨基氮含量,羧甲基纤维素酶、淀粉酶、酸性蛋白酶、漆酶胞外酶酶活生理生化指标,确立优化配方的液体菌种最优培养时间。以平均满袋时间为指标,确立液体菌种扩繁栽培种接种量、培养基配方颗粒度和碳氮比。[结果]优化得到大球盖菇液体菌种最优配方为葡萄糖 20 g·L-1、小麦粉30 g·L-1、酵母粉 0。75 g·L-1、磷酸二氢钾 1。00 g·L-1、硫酸镁 0。50 g·L-1、起始pH 5。培养第 8 天时,大球盖菇菌丝体生物量最大,为 1。66 g·hmL-1;液体培养过程中还原糖含量由 12。23 mg·mL-1 降至 1。38 mg·mL-1,氨基氮含量由 0。09 mg·mL-1 降至 0。06 mg·mL-1;羧甲基纤维素酶和淀粉酶酶活在第 4 天最高,酶活分别为 6。49、5。16 U,酸性蛋白酶酶活在第 2 天最高,酶活为 1。80 U,漆酶酶活在第 6 天最大,酶活为 1。63 U。液体菌种扩繁栽培种生产工艺参数:接种量为 15 mL,菌包培养基配方颗粒度的粗细木屑比为 7∶3,碳氮比为 50∶1。[结论]大球盖菇液体菌种活性与上述指标具有一定的相关性,结合发酵液生理生化指标,判定第 7天的液体菌种活力最高。利用大球盖菇液体菌种扩繁栽培种,平均满袋时间为 23。7 d,缩短生长周期 2。7 d。本研究建立配套的制种工艺,为大球盖菇栽培种工厂化生产技术奠定基础。
Propagating Stropharia rugosoannulata in Liquid Medium
[Objective]Propagating Stropharia rugosoannulata in liquid culture medium was studied.[Methods]S.rugosoannulata No.8 was cultivated in experimental media to determine the mycelial biomass increase in a single factor and orthogonal test L9(34)for formulation and culture conditions optimization.Mycelial biomass,reducing sugars,and amino nitrogen content as well as the extracellular enzyme activities of carboxymethyl cellulase,amylase,acid protease,and laccase of the culture were monitored to determine cultivation end point.Average full-bag filling time was used as indicator for the inoculation amount,substrate particle size,and carbon-to-nitrogen ratio in a maximized reproduction and yield.[Results]The optimized liquid culture medium was formulated with 20 g·L-1 glucose,30 g·L-1 wheat flour,0.75 g·L-1 yeast powder,1.00 g·L-1 potassium dihydrogen phosphate,and 0.50 g·L-1 magnesium sulfate at an initial pH of 5.On the 8th day of culture,the mycelial biomass reached a maximum at 1.66 g·h mL-1.As the mycelia grew,the reducing sugar in the medium decreased from 12.23 mg·mL-1 to 1.38 mg·mL-1 and the amino nitrogen from 0.09 mg·L-1 to 0.06 mg·L-1 during the culture process.The activities of carboxymethyl cellulase and amylase were the highest on the 4th day with the activities of 6.49 U and 5.16 U,respectively.The activity of acid protease peaked at 1.80 U on the 2nd day;and that of laccase,at 1.63 U on the 6th day.The inoculum production was best carried out with an inoculation of 15 mL,a coarse-to-fine ratio of 7∶3 on the substrate particle size,and a carbon-to-nitrogen ratio of 50∶1.[Conclusion]Since the viability of the mushroom propagation correlated with some of the physiological and biochemical indicators of the liquid medium,7 d was determined to be the peak for the cultivation.For filling a hyphal bag,23.7d of culture was required,which was 2.7d shorter than what needed without the optimization.The results provided the basis for the development of a scale-up industrial operation.

Stropharia rugosoannulataliquid culturemediumoptimizationapplication

曾志恒、戴建清、陈文智、曾辉、郭仲杰、蔡志欣

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福建省农业科学院食用菌研究所/特色食用菌繁育与栽培国家地方联合工程研究中心,福建 福州 350014

大球盖菇 液体菌种 培养基 优化 应用

福建省科技计划公益类专项宁夏回族自治区重点研发计划项目福建省农业科学院东西部协作项目

2021R10350022022BBF02022-04闽农科政[2023]8号

2024

福建农业学报
福建省农业科学院

福建农业学报

CSTPCD北大核心
影响因子:0.656
ISSN:1008-0384
年,卷(期):2024.39(6)