葡萄糖醛酸酶基因

IF 1.2 Q3 MULTIDISCIPLINARY SCIENCES ARO-THE SCIENTIFIC JOURNAL OF KOYA UNIVERSITY Pub Date : 2024-01-08 DOI:10.14500/aro.11239
H. Masyab, Qutaiba S. Al-Nema, Mozahim Q. Al-Mallah
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引用次数: 0

摘要

重氮葡萄糖醛酸杆菌以菌落的形式生活在植物组织细胞内,能排出约一半的固定氮,具有改善植物生长的潜在能力。本研究的目的是发现葡萄糖醛酸酶(GUS)标记的重氮乙酰杆菌与菠菜幼苗的相互作用,并使用 X-gluc 染料(5-溴-4-氯-3-吲哚基-β-D-葡萄糖醛酸)检测 GUS 基因。该 GUS 方案利用 X-gluc 染料进行化学检测,以检测菠菜幼苗组织中的 GUS 标记的重氮嗜血杆菌。结果表明,菠菜幼苗成功感染了 GUS 标记的重氮嗜血杆菌,幼苗在整个生长期都能存活,授粉幼苗的生长状况也有所改善。根切片的显微镜检查结果显示,细菌细胞存在于根尖,并集中在外围细胞的细胞壁区域。此外,子叶纵切片的显微镜检查结果显示,表皮细胞壁内存在大量细菌。这表明,这些细菌与菠菜幼苗之间相互作用的决定因素适合负责形成氮酶的基因的表达。
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Glucuronidase Gene
Gluconacetobacter diazotrophicus lives inside plant tissue cells in the form of colonies and excretes about half of the fixed nitrogen, which offers potential power that improves plant growth. The aim of this study is to find the interaction of glucuronidase (GUS)-labeled G. diazotrophicus with spinach seedlings and the detection of GUS genes using X-gluc dye (5-bromo-4-chloro-3-indolyl-β-D- glucuronic acid). The GUS protocol is used to detect GUS-labeled G. diazotrophicus in spinach seedling tissues by chemical detection using X-gluc dye. The results show that the spinach seedlings are successfully infected with GUS-labeled G. diazotrophicus , with the survival of the seedlings throughout their growth period and an improvement in the growth of pollinated seedlings. The outcomes of the microscopic inspection of the root slices reveal the presence of bacterial cells at the root tips and their concentration in the area of the cell walls of the peripheral cells. Furthermore, the findings of microscopic examinations of longitudinal sections for cotyledons show the presence of a number of bacteria within epidermal cell walls. This indicates that the determinants of the interaction between these bacteria and spinach seedlings are suitable for the expression of the gene responsible for the formation of the nitrogenase enzyme.
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来源期刊
ARO-THE SCIENTIFIC JOURNAL OF KOYA UNIVERSITY
ARO-THE SCIENTIFIC JOURNAL OF KOYA UNIVERSITY MULTIDISCIPLINARY SCIENCES-
自引率
33.30%
发文量
33
审稿时长
16 weeks
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