In [1]:
from pydna.all import *
In [2]:
p567,p577,p468,p467,p568,p578,p775,p778,p167,p166 = parse("yeast_pahtway_kit_standard_primers.txt")
In [3]:
from Bio.Restriction import ZraI, AjiI, EcoRV
In [4]:
pYPK0 =read("pYPK0.gb")
In [5]:
promoter_clone = pYPKa_Z_RPS19a =read("pYPKa_Z_RPS19a.gb")
In [6]:
gene_clone = pYPKa_A_ScRKI1 =read("pYPKa_A_ScRKI1.gb")
In [7]:
terminator_clone = pYPKa_E_TPI1 =read("pYPKa_E_TPI1.gb")
In [8]:
p =pcr( p167, p567, promoter_clone)
g =pcr( p468, p467, gene_clone)
t =pcr( p568, p166, terminator_clone)
In [9]:
pYPK0_E_Z, stuffer = pYPK0.cut((EcoRV, ZraI))
In [10]:
(pYPK0_E_Z, p, g, t)
Out[10]:
In [11]:
asm =Assembly((pYPK0_E_Z, p, g, t), limit=31)
In [12]:
asm
Out[12]:
In [13]:
candidate = asm.assemble_circular()[0]
candidate.figure()
Out[13]:
In [14]:
result = candidate.synced(pYPK0)
The new construct should have cseguid 79JiqIENZc7fgGgYo9WS44MLsBA
and 7703 bp.
In [15]:
print(len(result))
result.cseguid()
Out[15]:
In [16]:
result.name = "pMEC1132"
result.description = "pYPK0_RPS19a_ScRKI1_TPI1tp"
result.stamp()
Out[16]:
In [17]:
result.write("pYPK0_RPS19a_ScRKI1_TPI1.gb")
In [18]:
from pydna.all import *
In [19]:
reloaded =read("pYPK0_RPS19a_ScRKI1_TPI1.gb")
In [20]:
reloaded.cseguid()
Out[20]:
In [21]:
reloaded.description
Out[21]: