成熟度对‘红地球’葡萄氨基酸营养价值的影响

【目的】探明不同成熟度对‘红地球’葡萄氨基酸营养价值的影响。【方法】以不同成熟度(盛花期后88~123 d)的‘红地球’葡萄为试材,测定果实氨基酸含量。同时,以鸡蛋蛋白质为标准蛋白,WHO/FAO氨基酸参考模式为评价标准,进行氨基酸营养价值评估。【结果】‘红地球’葡萄至少包含18种氨基酸,包括8种必需氨基酸、2种儿童必需氨基酸。氨基酸含量随着采摘期变化而变化,其中必需氨基酸、非必需氨基酸、儿童必需氨基酸、药用氨基酸、支链氨基酸、增香与着色氨基酸、伯胺基氨基酸、特殊功效氨基酸含量(w,后同)分别为557.3~659.7、1 176.3~1 690.8、326.8~703.8、1 130.0~1 644.1、231.7~285.3、926.1~1 404.8、1 126.0~1 609.0、1 032.9~1 510.7 mg·kg^-1,组间差异显著(p <0.05),在完全成熟期Ⅰ达到峰值;精氨酸、天门冬氨酸和谷氨酸等风味氨基酸含量与其味觉阈值的比值分别介于2.62~6.31、4.50~5.47和4.64~6.09,随着采摘期的延长呈先升后降变化趋势。氨基酸评分、化学评分和氨基酸比值系数分依次为11.33~14.07、18.32~4.43、49.70~57.04。苯丙氨酸等8种氨基酸含量相对不足,赖氨酸和苏氨酸含量相对过剩。【结论】不同成熟度对‘红地球’葡萄氨基酸含量及其营养价值影响显著。     

辣椒秸秆复合基质对西瓜育苗质量的影响

为降低西瓜基质育苗生产成本,采用不同比例的辣椒秸秆与蛭石、珍珠岩进行复配,探讨其对西瓜幼苗形态建成及生理特性的影响,以明确最佳的草炭替代材料。试验设置L1(V_辣椒秸秆∶V_蛭石∶V_珍珠岩=1∶1∶1)、L2(V_辣椒秸秆∶V_蛭石∶V_珍珠岩=2∶1∶1)、L3(V_辣椒秸秆∶V_蛭石∶V_珍珠岩=4∶1∶1)3个处理和对照CK(V草炭∶V_蛭石∶V_珍珠岩=2∶1∶1)。结果表明,L2处理的西瓜幼苗株高、茎粗、叶片数、干鲜质量、根尖数、壮苗指数和根冠比最大,根系活力最高;L1处理的西瓜幼苗出苗率最高,但与L2差异不显著;L3处理的西瓜幼苗根长最大,但与L2差异不显著。L2处理的西瓜幼苗叶片叶绿素a、叶绿素b、叶绿素(a+b)、类胡萝卜素含量和净光合速率最高,较对照分别增加10.98%、11.51%、11.13%、7.71%和21.38%。因此,由辣椒秸秆、蛭石、珍珠岩体积比按2:1:1复合而成的育苗基质可以替代常规草炭育苗基质(V草炭∶V_蛭石∶V_珍珠岩=2∶1∶1)进行西瓜育苗。     

保安湖乌鳢渔获群体结构及生长特性

依据１９９２年和１９９３年４－５月收集的标本，分析保安湖乌鳢渔获体系结构和生长特征。年龄由Ⅰ－Ⅶ龄构成，Ⅰ－Ⅺ龄分别占渔获总尾数的１２．３７％，２４．７４％、４１．２４％和１７．５３％。Ⅴ－Ⅶ龄极少公占４．１２％。优势体长为３１－４２ｃｍ；优势体重为３５０－９５０ｇ。体长与体重关系为Ｗ＝０．００７９９１Ｌ＾３．１６０２。ＶｏｎＢｅｒｔａｌａｎｆｆｔｙ生长方程为Ｌｔ＝７７．３（１－ｅ＾－０．１９８８     

高浓度细胞分裂素诱导棉花悬浮细胞程序性死亡

棉花悬浮细胞经高浓度细胞分裂素（2mg／L KT或4mg／L KT）处理后第4天大量死亡，培养物呈褐黑色；抽提总DNA，进行琼脂糖胶电泳，结果表明：2mg／L KT和4mg／L KT两处理中有明显的大小为140～180bp及其倍增量片段的DNA“梯”。进行PI和FDA染色显微观察可以看到：2mg／L KT处理中大部分细胞的细胞核较小，核质浓缩，呈棒形或弯月形；胞质浓缩，出现了不对称的质壁分离，且丧失了FDA染色活性。这些结果表明，由高浓度细胞分裂素处理引起的棉花悬浮细胞大规模死亡是一种细胞程序性死亡（PCD）。不同的生理状态（UCSA和BAE）和不同生长时期（指数增长期和静止期）的棉花悬浮细胞对高浓度细胞分裂素的诱导反应存在差异。     

上海地区野鸟中伯氏疏螺旋体和西尼罗病毒感染的血清学调查

于2005年从飞抵上海的12种候鸟和4种留鸟中采集208份血清样品,采用酶联荧光测定(ELFA)法和酶联免疫吸附试验(ELISA),分别对伯氏疏螺旋体和西尼罗病毒的感染状况进行了血清抗体调查,结果受检野鸟样品的检测结果均为阴性。     

上海地区多种动物戊型肝炎血清学调查

在上海地区收集血液样品(猪、牛、山羊、马、鸡、鸭、鸽、犬和部分珍禽等)964份,应用双抗原夹心酶联免疫法(DS-ELISA)检测抗HEV抗体。结果表明,猪抗HEV抗体的阳性率为72.18%(301/417),其中母猪阳性率最高,为82.53%(222/269),育成猪阳性率为52.54%(62/118),保育猪阳性率为50.00%(15/30);22个猪场均检测到抗HEV抗体阳性猪,阳性率高于60%的猪场有16个,占阳性猪场的72.72%。在牛、山羊、马、鸡、鸭、鸽等血清中也检测到了抗HEV抗体,阳性率分别为6.00%,24.00%,16.00%,1.90%,12.77%和4.44%,明显低于猪群的阳性率。在宠物犬中检测到了抗体阳性犬,阳性率为17.82%(18/101),说明犬对HEV易感。珍禽中野鸭、火烈鸟对HEV也有一定的敏感性,阳性率分别为6.60%(1/15)和10%(1/10),在孔雀和鸵鸟的血清标本中未检测到HEV抗体。猪群中戊型肝炎病毒存在较普遍,其他与人类密切相关的多种动物也对HEV敏感。     

A Novel Gelatinase from Marine Flocculibacter collagenilyticus SM1988: Characterization and Potential Application in Collagen Oligopeptide-Rich Hydrolysate Preparation

Although the S8 family in the MEROPS database contains many peptidases, only a few S8 peptidases have been applied in the preparation of bioactive oligopeptides. Bovine bone collagen is a good source for preparing collagen oligopeptides, but has been so far rarely applied in collagen peptide preparation. Here, we characterized a novel S8 gelatinase, Aa2_1884, from marine bacterium Flocculibacter collagenilyticus SM1988^T, and evaluated its potential application in the preparation of collagen oligopeptides from bovine bone collagen. Aa2_1884 is a multimodular S8 peptidase with a distinct domain architecture from other reported peptidases. The recombinant Aa2_1884 over-expressed in Escherichia coli showed high activity toward gelatin and denatured collagens, but no activity toward natural collagens, indicating that Aa2_1884 is a gelatinase. To evaluate the potential of Aa2_1884 in the preparation of collagen oligopeptides from bovine bone collagen, three enzymatic hydrolysis parameters, hydrolysis temperature, hydrolysis time and enzyme-substrate ratio (E/S), were optimized by single factor experiments, and the optimal hydrolysis conditions were determined to be reaction at 60 ℃ for 3 h with an E/S of 400 U/g. Under these conditions, the hydrolysis efficiency of bovine bone collagen by Aa2_1884 reached 95.3%. The resultant hydrolysate contained 97.8% peptides, in which peptides with a molecular weight lower than 1000 Da and 500 Da accounted for 55.1% and 39.5%, respectively, indicating that the hydrolysate was rich in oligopeptides. These results indicate that Aa2_1884 likely has a promising potential application in the preparation of collagen oligopeptide-rich hydrolysate from bovine bone collagen, which may provide a feasible way for the high-value utilization of bovine bone collagen.     

优质脆李新品种‘中李5号’的选育

‘中李5号’李是以‘青脆李’为母本经自然实生选育而成。该品种生长势较强,树姿半开张;在河南省郑州市观察,3月上旬进入初花期,3月中旬进入盛花期,花期持续约10 d;果实发育期约120 d,于7月中旬成熟;果实近圆形,果顶扁平,缝合线浅,平均单果重46.8 g,果皮呈黄绿色,不着红色,果面有明显果粉层;果肉呈浅黄色,肉质细腻、硬脆,汁液多,纤维少,风味酸甜,无香气;果实可溶性固形物含量15.8%,维生素C含量6.82 mg/100 g,可溶性糖含量9.62%,可滴定酸含量0.82%,可食率97.9%;该品种5年生树的株产可达32 kg以上,丰产能力较强,在河南及周边省市李树适生区均可栽植。     

植原体引起雪花木小叶病在中国的首次报道

2022年首次在广州市发现园林植物雪花木小叶病病株, 采用分子生物学技术对其进行植原体的种类鉴定。以雪花木叶片总DNA为模板, 利用植原体16S rRNA通用引物P1/P7进行PCR扩增, 获得广东雪花木小叶病植原体(BLL-GD2022)16S rRNA基因片段(1 811 bp, GenBank登录号为OQ625536)。16S rRNA序列相似性显示, BLL-GD2022与16SrVI组植原体株系的相似性最高, 为97.05%~99.83%, 其中与隶属于16SrVI-D亚组的10个植原体株系相似性为99.21%~99.83%。系统进化分析显示, BLL-GD2022与16SrVI组各植原体株系聚类在一个大分支, 其中与16SrVI-D亚组成员聚类在一个小分支, 亲缘关系最近。基于16S rRNA序列的iPhyClassifier限制性内切酶虚拟RFLP分析表明, BLL-GD2022与16SrVI-D亚组的参考株系Brinjal little leaf phytoplasma (GenBank登录号为X83431)的酶切图谱一致, 相似系数为1.00。基于上述研究结果, 明确广州市雪花木小叶病植原体隶属16SrVI-D亚组成员。本研究首次在园林植物雪花木上检测到植原体, 通过16S rRNA序列分析明确为16SrVI-D亚组成员, 为开展16SrVI-D亚组植原体在蔬菜、花卉和园林植物的发生监测及病害防控提供科学依据。     

MicroLEIS: A microcomputer-based Mediterranean land evaluation information system

Abstract. A computer-based land evaluation information system (MicroLEIS) was developed for optimal use of agricultural and forestry land systems under Mediterranean conditions. Through an interactive procedure several land capability, suitability and yield prediction methods may be applied. The system addresses land evaluation at reconnaissance, semi-detailed and detailed scales in an interrelated manner. Biophysical land evaluation methods are incorporated using empirical, scale-appropriate models, which range from purely qualitative (reconnaissance) through semi-quantitative (semi-detailed) to quantitative (detailed). This software is helpful for teaching, research and development, predicting appropriate agroforestry land uses. Its use is illustrated by an example.
MicroLEIS runs on IBM PC, XT, AT, or a compatible microcomputer with at least 128 kilobytes of RAM and a PC-DOS or MS-DOS version 2.0 or later operating system. The software package on double or high density diskettes can be obtained from the first author.