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一种制备均匀菌丝体悬浮液新方法的评估

Evaluation of a new method for the preparation of homogeneous mycelial suspensions.

作者信息

GUIDRY D J, TRELLES G H

出版信息

J Bacteriol. 1962 Jan;83(1):53-60. doi: 10.1128/jb.83.1.53-60.1962.

Abstract

Guidry, D. J. (Louisiana State University, New Orleans) and G. H. Trelles. Evaluation of a new method for the preparation of homogeneous mycelial suspensions. J. Bacteriol. 83:53-60. 1962.-An all-glass tissue homogenizer (providing both conical and cylindrical grinding surfaces) was employed in the preparation of homogeneous mycelial suspensions. Pellets of mycelium from constant shake liquid culture were submitted to grinding for various periods of time. The effect of grinding time on optical density of the homogenate, hyphal fragment size, and viability of the fungus was determined. A grinding time of 4 min was found to yield suspensions of mycelium in which 89% of the hyphal fragments contained four or less than four cells. Optical density was used as the basis for both preparation of standard samples of inoculum and measurement of growth. Preparation of a light transmittance curve facilitates the preparation of suspensions of any desired concentration. Although plate colony counts on samples from the same flask showed satisfactory agreement, there was appreciable variation in counts on samples from different flasks. The variation in growth from flasks receiving equal samples of inoculum was also determined. Results indicate that, at concentrations of mycelium equal to an optical density of 0.301, a difference of 15% or more in the optical density of two samples (10 flasks per sample) can be accepted as significant. Some of the factors influencing variation in viability of inoculum as well as variation in flask growth have been determined. Ways in which experimental errors can be kept to a minimum are discussed.

摘要

吉德里,D. J.(路易斯安那州立大学,新奥尔良)和G. H. 特雷列斯。一种制备均匀菌丝体悬浮液新方法的评估。《细菌学杂志》83:53 - 60。1962年。——使用一种全玻璃组织匀浆器(提供圆锥形和圆柱形研磨表面)来制备均匀的菌丝体悬浮液。将来自持续振荡液体培养的菌丝体小球进行不同时间段的研磨。测定了研磨时间对匀浆光密度、菌丝片段大小和真菌活力的影响。发现研磨4分钟可得到菌丝体悬浮液,其中89%的菌丝片段含有四个或少于四个细胞。光密度既用作接种物标准样品制备的基础,也用作生长测量的基础。制备透光率曲线有助于制备任何所需浓度的悬浮液。尽管来自同一烧瓶的样品平板菌落计数显示出令人满意的一致性,但来自不同烧瓶的样品计数存在明显差异。还测定了接受等量接种物样品的烧瓶中生长的差异。结果表明,在菌丝体浓度等于光密度0.301时,两个样品(每个样品10个烧瓶)光密度相差15%或更多可被视为显著差异。已经确定了一些影响接种物活力变化以及烧瓶生长变化的因素。讨论了将实验误差保持在最低限度的方法。

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