Uddin Mohammad Mosleh, Lima Suzana Afrin, Hossain Tanim Jabid, Kar Newton, Zahan Yeasmin, Olarewaju Babamale AbdulKareem
Department of Biochemistry and Molecular Biology, Mawlana Bhashani Science and Technology University, Santosh, Tangail 1902, Bangladesh.
Department of Biochemistry and Molecular Biology, University of Chittagong, Chittagong 4331, Bangladesh.
Trop Life Sci Res. 2021 Sep;32(3):53-68. doi: 10.21315/tlsr2021.32.3.4. Epub 2021 Sep 30.
Insects of the taxonomic order Coleoptera are recognised for considerable cellulolytic activity in their digestive fluid. The cellulolytic activity of the gut fluid in , a member of Coleoptera, however, remains unexplored. In this study, we, for the first time, report the qualitative and quantitative analysis of cellulolytic activity in the digestive fluid of this insect. The cellulolytic endo-1,4-β-D-glucanase activity was confirmed in the supernatant of the insect's digestive fluid by agar plate assay using carboxymethyl cellulose as the substrate. To determine the optimum pH, enzyme activity was further assessed in an acidic pH range of 5 to 6, and the highest activity was observed at pH 5.3. For quantitative analysis, endoglucanase activity was measured using 3,5-dinitrosalicylic acid method which revealed that the specific activity of the gut sample was 0.69 (±0.01) units per mg of protein. For further characterisation of the cellulases in the sample, SDS-PAGE and zymogram analysis were carried out. Two active cellulolytic bands were detected on the zymogram suggesting the presence of two distinct endoglucanases which completely disappeared upon heating the sample at 55°C. Our study, therefore, highlights prospect of the gut fluid of as an important source of cellulase enzymes that merits further investigations into their extensive characterisation for potential industrial applications.
鞘翅目昆虫因其消化液中具有相当的纤维素分解活性而闻名。然而,作为鞘翅目一员的[昆虫名称未给出]肠道液的纤维素分解活性仍未被探索。在本研究中,我们首次报告了对这种昆虫消化液中纤维素分解活性的定性和定量分析。通过以羧甲基纤维素为底物的琼脂平板试验,在昆虫消化液的上清液中证实了纤维素分解内切 - 1,4 - β - D - 葡聚糖酶活性。为了确定最佳pH值,在5至6的酸性pH范围内进一步评估酶活性,在pH 5.3时观察到最高活性。对于定量分析,使用3,5 - 二硝基水杨酸法测量内切葡聚糖酶活性,结果表明肠道样品的比活性为每毫克蛋白质0.69(±0.01)单位。为了进一步表征样品中的纤维素酶,进行了SDS - PAGE和酶谱分析。在酶谱上检测到两条活性纤维素分解带,表明存在两种不同的内切葡聚糖酶,在55°C加热样品后它们完全消失。因此,我们的研究突出了[昆虫名称未给出]肠道液作为纤维素酶重要来源的前景,值得对其进行更广泛的表征以用于潜在的工业应用进行进一步研究。