首页> 外文会议>Australian Society of Sugar Cane Technologists Conference >ISOLATION OF PROTOPLASTS AND VACUOLES FROM SUGARCANE SUSPENSION AND STEM PARENCHYMA CELLS
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ISOLATION OF PROTOPLASTS AND VACUOLES FROM SUGARCANE SUSPENSION AND STEM PARENCHYMA CELLS

机译:从甘蔗悬浮液和茎妥亚细胞中分离原生质体和液压液

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The vacuole is a compartment within sugarcane cells in which most of the sucrose is stored. Despite its importance, the sugarcane vacuole is not well understood, because it has been very difficult to examine from sucrose-accumulating stem cells. It is only separated from other cell components by a single membrane which is generally broken during attempts to isolate the vacuole for study. One new approach to sugarcane improvement is to direct novel enzymes into the vacuole to convert sucrose into higher value biomaterials. Unfortunately, the vacuole is very acidic and it also contains proteolytic enzymes that seem to degrade most introduced enzymes before they can perform useful bioconversions. This new potential led us to revisit the challenge of vacuole isolation from mature sugarcane stems. Our immediate interest was to use the isolated vacuoles to understand how to stabilise introduced enzymes. They would also be very useful in studies to understand how sugarcane achieves its exceptional stored sugar concentrations. A first step to vacuole isolation is the removal of the cellulose walls surrounding sugarcane cells, yielding protoplasts. So we developed a method to isolate protoplasts from sugarcane immature and mature stem parenchyma cells by: (ⅰ) using an enzyme solution containing cellulase onozuka RS, macerozyme, pectinase and driselase; (ⅱ) adjusting the solution to match the internode osmotic strength; (ⅲ) pretreating internodes at 4°C for 1-2 days before the enzyme treatment; (ⅳ) vacuum infiltration of tissues in enzyme solution and changing the solution after 1-2 hours of incubation; (ⅴ) purification of protoplasts in Ficoll gradients. However, osmotic lysis of these protoplasts yielded less than 2% of vacuoles in most trials and polybase-induced lysis did not yield any vacuoles.
机译:芳氢是甘蔗细胞内的隔室,其中大多数蔗糖被储存。尽管重要的是,甘蔗液泡并不熟知,因为从蔗糖积聚干细胞中难以检查。它仅通过单个膜与其他细胞组分分离,所述单个膜通常在试图分离液泡中进行研究时被破裂。甘蔗改善的一种新方法是将新酶直接进入液泡中以将蔗糖转化为更高价值的生物材料。不幸的是,液泡是非常酸性的,它还含有蛋白水解酶,似乎在它们进行有用的生物释放物之前似乎降低了大多数引入的酶。这种新潜力导致我们重新审视从成熟甘蔗茎的液泡分离的挑战。我们的立即兴趣是使用隔离的液体来了解如何稳定引入的酶。他们在研究中也非常有用,以了解甘蔗如何实现其卓越的储存糖浓度。漂浮隔离的第一步是除去甘蔗细胞周围的纤维素壁,产生原生质体。因此,我们开发了一种从甘蔗未成熟和成熟干预细胞中分离出原生质体的方法:(Ⅰ)使用含有纤维素酶Onozuka Rs,MeSerozyme,果胶酶和纱序列的酶溶液; (Ⅱ)调节溶液匹配节间渗透强度; (Ⅲ)在酶处理前1-2天预处理4°C的间隙; (ⅳ)酶溶液中组织的真空浸润,并在孵育1-2小时后改变溶液; (ⅴ)氟叶梯度纯化原生质体。然而,在大多数试验中,这些原生质体的渗透溶解在大多数试验中产生少于2%的真空液,并且聚酶诱导的裂解不产生任何真空粘附。

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