Harpinpsta from Pseudomonas syringae pv. tabaci Is Defective and Deficient in Its Expression and HR-inducing Activity     

Fumiko TAGUCHI  Rui TANAKA  Sayuri KINOSHITA  Yuki ICHINOSE  Yoshiyuki IMURA  Salamah ANDI  Kazuhiro TOYODA  Tomonori SHIRAISHI  Tetsuji YAMADA 《Journal of General Plant Pathology》2001,67(2):116-123

To elucidate the role of harpins produced by Pseudomonas syringae, the corresponding hrpZ gene was isolated from P. s. pv. tabaci. The sequence information revealed that this gene carries a serious mutation with 326 bp lacking in the central region and potentially encodes only 140 N-terminal amino acids because of a frame shift. The investigation of biological properties using recombinant harpin indicated harpin_psta was incapable of inducing HR in both host and nonhost plants. Based on an immunoblot analysis to detect harpin from P. s. pathovars in hrp-inducing medium, the truncated harpin_psta was neither expressed nor secreted into the culture medium. These results suggest that harpin is not the sole determinant of the host-parasite specificity in P. s. pv. tabaci. Received 10 August 2000/ Accepted in revised form 21 December 2000  相似文献   

Determination of 2-thiocyanomethylthiobenzothiazole (TCMTB) in treated wood and wood preservative using Ultraviolet–visible spectrophotometer     

K. Tumirah  S. Salamah  A. Rozita  U. Salmiah  M. A. M. Nasir 《Wood Science and Technology》2012,46(6):1021-1031

Ultraviolet–visible Spectrophotometer method for the determination of 2-thiocyanomethylthiobenzothiazole (TCMTB) in treated wood and wood preservative was developed. The determination was done after conversion of TCMTB to 2-mercaptobenzothiazole (2-MBT). This conversion was obtained by reaction with 0.1?M cystein alkaline condition (pH 10). The extraction of 2-MBT was carried out with ethyl acetate containing 0.2% of ?-mercaptoethanol after acidification with 2?M phosphoric acid (pH 2.5). The sample absorbance was measured at 324?nm wavelength with a calibration curve range from 10 to 90?ppm of TCMTB. The Regression value, R ², achieved was 0.9998, while the precision, RSD, was <10% (n?=?6). The recovery was in the range of 90.7–103.2% (n?=?6). The result obtained with this colorimetric procedure is comparable to the HPLC–PDA method.  相似文献