矾根主要品种的叶色表型性状分析

通过目测进行分类的方式很难准确界定矾根品种叶色。为建立一套更为科学的基于叶色表型的矾根品种分类体系,笔者利用色差仪对72个矾根品种共计432个样品的叶色进行测定,对获得的L、a、b 3个色度值进行聚类分析,将72个矾根品种分为褐色系、深绿色系、黄色系、灰绿色系、浅绿色系5类色系。对矾根品种各色系的L、a、b值进行相关性分析,发现叶片正面的L值与a值、a值与b值呈负相关,L值与b值呈正相关,但相关性不明显;叶片背面的L值与a值、a值与b值呈负相关,L值与b值呈显著正相关。从多重比较的结果中可以看出,矾根品种各色系之间的L、a、b色度值差异显著,尤其是各色系间叶正面的颜色差异较大,在矾根品种选育工作中,叶片正面的颜色将作为主要参考。     

农村电网配电台区智能化改造及系统建设

强调了加强农村电网配电台区智能化改造及系统建设的重要性，阐述了农村电网配电台区的构成情况。重点以某农村地区为例，提出并实施了相应改造措施，评价了改造效果。      

The M43 domain-containing metalloprotease RcMEP1 in Rhizoctonia cerealis is a pathogenicity factor during the fungus infection to wheat

Wheat(Triticum aestivum L.) is an important staple crop for global human. The necrotrophic fungus Rhizoctonia cerealis is the causal pathogen of sharp eyespot, a devastating disease of wheat. Herein, we identified RcMEP1, a zinc metalloproteaseencoding gene from R. cerealis genomic sequences, and characterized its pathogenesis function. RcMEP1 expressed at markedly-high levels during R. cerealis infection process to wheat. The predicted protein RcMEP1 comprises of 287 amino acid residues and contains a signal peptide and a M43 metalloprotease domain harboring the active site motif(HEVGHWLGLYH). The assays of Agrobacterium tumefaciens-mediated transient expression in Nicotiana benthamiana leaves indicated that RcMEP1 is an apoplastic elicitor of cell death, and that the predicted signal peptide functions and is required for secretion and cell death-induction. The purified RcMEP1 protein and its M43 domain peptide were individually able to induce plant cell death and H2 O2 accumulation, and to inhibit expression of host chitinases when infiltrated into wheat and N. benthamiana leaves, while the M43 domain-deleting peptide and negative control lacked the capacity. Moreover, compared with the control pretreatment, the purified RcMEP1 protein or its M43-domain peptide resulted in enhanced pathogenesis in the inoculated wheat, whereas the M43 domain-deleting peptide failed. These results suggest that RcMEP1 acted as an important pathogenicity factor during R. cerealis infection to wheat and that its signal peptide and M43 domain are required for the secretion and pathogenesis of RcMEP1. This study provides insights into pathogenesis role of M43 domain-containing metalloproteases during R. cerealis infection to wheat.     

Effect of dietary calcium or phosphorus deficiency on bone development and related calcium or phosphorus metabolic utilization parameters of broilers from 22 to 42 days of age

This experiment was conducted to investigate the effect of dietary calcium (Ca) or phosphorus (P) deficiency on bone development and related Ca or P metabolic utilization parameters of broilers from 22 to 42 days of age based on our previous study, which indicated that dietary Ca or P deficiency impaired the bone development by regulating related Ca or P metabolic utilization parameters of broilers from 1 to 21 days of age. A total of 504 one-day-old Arbor Acres male broilers were randomly assigned to 1 of 4 treatments with 7 replicates in a completely randomized design, and fed the normal control and Ca- or P-deficient diets from 1 to 21 days of age. At 22 days of age, the broilers were further fed the normal control diet (0.90% Ca+0.35% non-phytate P (NPP)), the P-deficient diet (0.90% Ca+0.18% NPP), the Ca-deficient diet (0.30% Ca+0.35% NPP) or the Ca and P-deficient diet (0.30% Ca+0.18% NPP), respectively. The results showed that dietary Ca or P deficiency decreased (P<0.05) tibia bone mineral density (BMD), bone breaking strength (BBS), ash content, tibia ash Ca content and serum P content on days 28 and 42, but increased (P<0.05) tibia alkaline phosphatase (ALP) activity of broilers on day 42 compared with the control group. Furthermore, the broilers fed the P-deficient diet had the lowest (P<0.05) tibia BMD, BBS, ash content, serum P content and the highest (P<0.05) serum Ca content on day 28 compared with those fed the Ca-deficient or Ca and P-deficient diets. The results from the present study indicated that the bone development and related Ca or P metabolic utilization parameters of broilers were the most sensitive to dietary P deficiency, followed by dietary Ca deficiency or Ca and P-deficiency; dietary Ca or P deficiency impaired the bone development possibly by regulating serum Ca and P contents as well as tibia Ca content and ALP activity of broilers from 22 to 42 days of age.     

基于网络嵌入性的我国东北国有林区知识转移机理

文中从社会网络视角分析我国东北国有林区职工、家庭及林业企业知识转移的过程和影响因素，以期通过社会关系和网络结构促进林业企业转型。应用知识转移基本理论构建东北国有林区多层次知识转移理论模型，在此基础上从社会网络视角分析林区职工、家庭和林业企业3个层面的知识转移机理。研究表明:增强林区知识转移个体与利益相关者的联系程度、占据更多的结构洞位置以及提高个体网络中心度和凝聚程度有利于知识获取和内化；林区待岗职工与利益相关者的弱联系有利于其获得更多就业机会；国有森工企业由于过度嵌入社会网络，知识内化和创新动力不足。     

贮运条件对草莓主要色素成分稳定性的影响

草莓在贮藏和运输期间会产生褪色现象,花青素含量逐渐减少。为研究光照时间、温度、pH、金属离子对草莓花青素的影响,探索合适的加工与贮运条件,在花青素含量保持一致的情况下设置4种反应条件,探讨光照时间、温度、pH、金属离子对草莓花青素的影响。草莓花青素在自然光下照射8 h,吸光度值下降25%,温度高于60℃后,吸光度值下降67%。当pH>7时,吸光度值下降85%,添加Na⁺、Mg²⁺后的色素提取液反应2 h后所测吸光度值分别保持在0.070和0.050左右,而添加Fe³⁺后测得的吸光度值下降87%。实验结果表明,草莓在贮运过程中应避光、低温、保持酸性条件,且避免与铁制品接触。     

软枣猕猴桃叶片愈伤组织诱导技术的研究

[目的]由于软枣猕猴桃在初代培养中外植体诱导率极低且快繁效果差,因此进行其组织培养技术体系的研究,以期解决其人工种植的难题.[方法]本研究以软枣猕猴桃展叶为外植体,通过采用不同消毒试剂及消毒处理时间,筛选出最佳的灭菌程序;将不同培养基与不同浓度的KT、2,4-D组合,筛选出最佳的初代培养基配方.[结果]选用展叶为外植体,75％CH3CH2OH处理30 s后以10％NaClO处理20 min,0.1％HgCl2处理15 min后无菌水冲洗3～4次,接至pH=5.8的MS+1 mg·L-1 KT+0.5 mg·L-12,4-D+3％白糖+0.55％琼脂培养基上,置于光照2500 lx、8 h·d-1,26℃下培养8 d后有少部分愈伤组织出现,60 d后平均单芽愈伤组织达0.8 g以上,平均单个愈伤组织长度0.7～1.4 cm,属中块愈伤组织.[结论]以本实验得出的愈伤组织培养方法进行培养,可有效提高诱导率,达到快繁的目的.     

花生壳黄酮的提取纯化工艺

本文采用酶法预处理结合超声波辅助提取的方式，最大程度地提高了花生壳总黄酮的得率，并优化大孔树脂纯化工艺，提高了有效成分的纯度。花生壳黄酮的最佳提取工艺为：花生壳粉与水混合，半纤维素酶与木聚糖酶按1:1（m/m）复配，用量0.25‰，50℃酶解30 min后，按料液比1:20（m/V）加入乙醇至终浓度60%，于功率1000 W，55℃超声波辅助提取60 min，花生壳总黄酮的得率约为2.5%。选用D101型大孔树脂，上样缓冲液为pH 5.0的60%乙醇溶液，洗脱液为pH 10.0的70% 乙醇溶液，上样与洗脱流速为0.75 BV/h和1.5 BV/h。纯化后的花生壳总黄酮和木犀草素的纯度分别为10.54%和5.85%，提高了90%和120%。     

Bamboo NiR gene is associated with regeneration capacity

It was reported that the activity of NiR (nitrite reductase) enzyme encoded by the NiR gene was correlated with the regeneration ability in rice. To testify the function of NiR gene in bamboo, seven bamboo species whose calli had different differentiation rate were chosen to analyse their NiR enzyme activity. The results showed that bamboo NiR enzymatic activity had a certain correlation with the regeneration capacity. A NiR gene named DhNiR from Dendrocalamus hamiltonii with high regeneration capacity was cloned. Sequence analysis revealed that the ORF of DhNiR was 1779bp encoding 592 amino acids. Overexpression of DhNiR in rice reduced the time of shoot differentiation and increased the transformation rate, suggesting that DhNiR might play an important role in the regeneration ability of bamboo, and can be applied in regeneration and gene transformation of bamboo and other plant species.