Ibrahim Darah, Weloosamy Haritharan, Lim Sheh-Hong
Darah Ibrahim, Haritharan Weloosamy, Sheh-Hong Lim, Industrial Biotechnology Research Laboratory, School of Biological Sciences, Universiti Sains Malaysia, 11800 Penang, Malaysia.
World J Biol Chem. 2015 Aug 26;6(3):265-71. doi: 10.4331/wjbc.v6.i3.265.
To investigate the impact of agitation speed on pectinase production and morphological changing of Aspergillus niger (A. niger) HFD5A-1 in submerged fermentation.
A. niger HFM5A-1 was isolated from a rotted pomelo. The inoculum preparation was performed by adding 5.0 mL of sterile distilled water containing 0.1% Tween 80 to a sporulated culture. Cultivation was carried out with inoculated 1 × 10(7) spores/mL suspension and incubated at 30 °C with different agitation speed for 6 d. The samples were withdrawn after 6 d cultivation time and were assayed for pectinase activity and fungal growth determination. The culture broth was filtered through filter paper (Whatman No. 1, London) to separate the fungal mycelium. The cell-free culture filtrate containing the crude enzyme was then assayed for pectinase activity. The biomass was dried at 80 °C until constant weight. The fungal cell dry weight was then expressed as g/L. The 6 d old fungal mycelia were harvested from various agitation speed, 0, 50, 100, 150, 200 and 250 rpm. The morphological changing of samples was then viewed under the light microscope and scanning electron microscope.
In the present study, agitation speed was found to influence pectinase production in a batch cultivation system. However, higher agitation speeds than the optimal speed (150 rpm) reduced pectinase production which due to shear forces and also collision among the suspended fungal cells in the cultivation medium. Enzyme activity increased with the increasing of agitation speed up to 150 rpm, where it achieved its maximal pectinase activity of 1.559 U/mL. There were significant different (Duncan, P < 0.05) of the pectinase production with the agitation speed at static, 50, 100, 200 and 250 rpm. At the static condition, a well growth mycelial mat was observed on the surface of the cultivation medium and sporulation occurred all over the fungal mycelial mat. However with the increased in agitation speed, the mycelial mat turned slowly to become a single circular pellet. Thus, it was found that agitation speed affected the morphological characteristics of the fungal hyphae/mycelia of A. niger HFD5A-1 by altering their external as well as internal cell structures.
Exposure to higher shear stress with an increasing agitation speed could result in lower biomass yields as well as pectinase production by A. niger HFD5A-1.
研究搅拌速度对黑曲霉HFD5A-1在深层发酵中果胶酶产量及形态变化的影响。
从腐烂柚子中分离得到黑曲霉HFM5A-1。接种体制备是向产孢培养物中加入5.0 mL含0.1%吐温80的无菌蒸馏水。用接种1×10(7)个孢子/mL的悬浮液进行培养,在30℃下以不同搅拌速度培养6天。培养6天后取出样品,测定果胶酶活性和真菌生长情况。将培养液通过滤纸(Whatman No. 1,伦敦)过滤以分离真菌菌丝体。然后测定含粗酶的无细胞培养液的果胶酶活性。将生物质在80℃下干燥至恒重。真菌细胞干重以g/L表示。从不同搅拌速度(0、50、100、150、200和250 rpm)下培养6天的真菌菌丝体中收获样品。然后在光学显微镜和扫描电子显微镜下观察样品的形态变化。
在本研究中,发现搅拌速度在分批培养系统中会影响果胶酶的产量。然而,高于最佳速度(150 rpm)的搅拌速度会降低果胶酶产量,这是由于剪切力以及培养介质中悬浮真菌细胞之间的碰撞所致。酶活性随着搅拌速度增加到150 rpm而增加,此时达到其最大果胶酶活性1.559 U/mL。在静态、50、100、200和250 rpm的搅拌速度下,果胶酶产量存在显著差异(邓肯检验,P < 0.05)。在静态条件下,在培养基表面观察到生长良好的菌丝垫,并且在整个真菌菌丝垫上发生产孢。然而,随着搅拌速度的增加,菌丝垫逐渐变成单个圆形菌球。因此,发现搅拌速度通过改变黑曲霉HFD5A-1真菌菌丝/菌丝体的外部以及内部细胞结构来影响其形态特征。
随着搅拌速度增加而暴露于更高的剪切应力下,可能导致黑曲霉HFD5A-1的生物量产量以及果胶酶产量降低。