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Caulobacter crescentus
June
1.With the help of Mr. Wanshun Ma and Qiong Guo from Beijing Institute of Nanoenergy and Nanosystems, Chinese Academy of Science(CAS), we got Caulobacter crescentus CB15 from ATCC.
2.We got E. coli S17-1 from Professor Tao Zhu in University of Science and Technology of Tianjin and also as key scientist of Cansino, which would be utilized for conjugation with C. crescentus.
3.Experiment Practice.
July 30th 1. Preparation of competent bacteria S17-1 and using it, red fluorescent protein (mRFP) was successfully transformed.
July 2nd 1. Start construction of the first shuttle plasmid for conjugation OriT-RFP.
July 4th With bacterial colony PCR, we were attempting to get DgrA and DgrB, which are indispensable for flagellum synthesis and fortunately, DgrA band appeared.
July 5th Again using bacterial colony PCR, we got DgrB band.
July 22nd Construct OriT-RFP plasmid using 3A assembly methods.
July 26th Successfully constructed Orit-RFP plasmid and made a conjugation using it. Though it seemed worked, results from electrophoresis were not exactly correct. The reason was unknown.
August 6th Trying to guide the plasmid into* C. crescentus* by electrotransformation, including the preparation of competent cell and electrotransformation procedure. This method was tried 6 times in August, but it failed again and again. Finally, we had no alternative but to try on conjugation again.
August 8th Redesign the primer used for standardization of DgrA, DgrB and HfiA which controls the biosynthesis of holdfast.
August 9th Add promoter on DgrA, DgrB and HfiA.
August 21st Failing to get the correct sequence of R0051-DgrA, we all ascribe to promoter in Parts.
August 24th Ligate DgrA with K592020.
September 25th Construction of R0082-HfiA, OriT-K592020 and OriT-K592016 have been accomplished. September 26th Alter the carrier and standardization of DgrA, DgrB and HfiA.
September Conjugate OriT-K592020 into C. crescentus
