Zhang F., Lin J. J., Fox T. C., Mujer C. V., Rumpho M. E., Kennedy R. A.
Departments of Horticultural Sciences (T.C.F., C.V.M., M.E.R.) and Biology (R.A.K.), Texas A&M University, College Station, Texas 77843.
Plant Physiol. 1994 Aug;105(4):1149-1157. doi: 10.1104/pp.105.4.1149.
Echinochloa species differ in their ability to germinate and grow in the absence of oxygen. Seeds of Echinochloa crus-pavonis (H.B.K.) Schult do not germinate under anoxia but remain viable for extended periods (at least 30 d) when incubated in an anaerobic environment. E. crus-pavonis can be induced to germinate and grow in an anaerobic environment if the seeds are first subjected to a short (1-18 h) exposure to aerobic conditions (aerobic priming). Changes in polypeptide patterns (constitutive and de novo synthesized) and protein phosphorylation induced by aerobic priming were investigated. In the absence of aerobic priming protein degradation was not evident under anaerobic conditions, although synthesis of a 20-kD polypeptide was induced. During aerobic priming, however, synthesis of 37- and 55-kD polypeptides was induced and persisted upon return of the seeds to anoxia. Furthermore, phosphorylation of two 18-kD polypeptides was observed only in those seeds that were labeled with 32PO4 during the aerobic priming period. Subsequent chasing in an anaerobic environment resulted in a decrease in phosphorylation of these polypeptides. Likewise, phosphorylation of the 18-kD polypeptides was not observed if the seeds were labeled in an anaerobic atmosphere. These results suggest that the regulated induction of the 20-, 37-, and 55- kD polypeptides may be important for anaerobic germination and growth of E. crus-pavonis and that the specific phosphorylation of the 18-kD polypeptides may be a factor in regulating this induction.
稗属植物在无氧条件下的发芽和生长能力存在差异。稗草(Echinochloa crus-pavonis (H.B.K.) Schult)的种子在缺氧条件下不发芽,但在厌氧环境中培养时能长时间保持活力(至少30天)。如果稗草种子先经过短时间(1 - 18小时)的有氧条件处理(有氧引发),则可在厌氧环境中诱导发芽和生长。研究了有氧引发诱导的多肽模式(组成型和从头合成型)变化以及蛋白质磷酸化情况。在没有有氧引发的情况下,厌氧条件下蛋白质降解不明显,尽管诱导合成了一种20-kD的多肽。然而,在有氧引发期间,诱导合成了37-kD和55-kD的多肽,并且在种子回到缺氧状态后这些多肽仍持续存在。此外,仅在有氧引发期间用32PO4标记的那些种子中观察到两种18-kD多肽的磷酸化。随后在厌氧环境中追踪导致这些多肽的磷酸化减少。同样,如果种子在厌氧气氛中标记,则未观察到18-kD多肽的磷酸化。这些结果表明,20-kD、37-kD和55-kD多肽的调控诱导可能对稗草的厌氧发芽和生长很重要,并且18-kD多肽的特异性磷酸化可能是调节这种诱导的一个因素。